Autophagy and the immune function in aging

A role for mitochondria in nlrp3 inflammasome activation

Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602 · see citing works

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 · see citing works

Autophagy and the Integrated Stress Response

Kroemer, G., Mariño, G., & Levine, B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.023 · Cited by 3,506 · see citing works

Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome

Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049 · see citing works

Thioredoxin-interacting protein links oxidative stress to inflammasome activation

Zhou, R., Tardivel, A., Thorens, B., Choi, I., & Tschopp, J. (2010) · Nature Immunology · doi:10.1038/ni.1831 · Cited by 2,708 · see citing works

Oxidized mitochondrial DNA activates the NLRP3 inflammasome during apoptosis

Shimada, K., Crother, T. R., Karlin, J., Dagvadorj, J., Chiba, N., Chen, S., Ramanujan, V. K., Wolf, A. J., Vergnes, L., Ojcius, D. M., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.01.009 · Cited by 2,282 · see citing works

Autophagy and Aging

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

Mammalian autophagy: core molecular machinery and signaling regulation

Yang, Z., & Klionsky, D. J. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2009.11.014 · Cited by 1,956 · see citing works

Autophagy in infection, inflammation and immunity

Deretic, V., Saitoh, T., & Akira, S. (2013) · Nature Reviews Immunology · doi:10.1038/nri3532 · Cited by 1,919 · see citing works

A key role for autophagy and the autophagy gene Atg16l1 in mouse and human intestinal Paneth cells

Cadwell, K., Liu, J. Y., Brown, S. L., Miyoshi, H., Loh, J., Lennerz, J. K., Kishi, C., Kc, W., Carrero, J. A., Hunt, S., et al. (2008) · Nature · doi:10.1038/nature07416 · Cited by 1,542 · see citing works

Activation of autophagy by inflammatory signals limits IL-1β production by targeting ubiquitinated inflammasomes for destruction

Shi, C.-S., Shenderov, K., Huang, N.-N., Kabat, J., Abu-Asab, M., Fitzgerald, K. A., Sher, A., & Kehrl, J. H. (2012) · Nature Immunology · doi:10.1038/ni.2215 · Cited by 1,367 · see citing works

Toll-like receptor signalling in macrophages links the autophagy pathway to phagocytosis

Sanjuan, M. A., Dillon, C. P., Tait, S. W. G., Moshiach, S., Dorsey, F., Connell, S., Komatsu, M., Tanaka, K., Cleveland, J. L., Withoff, S., et al. (2007) · Nature · doi:10.1038/nature06421 · Cited by 1,347 · see citing works

Autophagy Genes Are Essential for Dauer Development and Life-Span Extension in <i>C. elegans</i>

Meléndez, A., Tallóczy, Z., Seaman, M., Eskelinen, E.-L., Hall, D. H., & Levine, B. (2003) · Science · doi:10.1126/science.1087782 · Cited by 1,270 · see citing works

Discovery of Atg5/Atg7-independent alternative macroautophagy

Nishida, Y., Arakawa, S., Fujitani, K., Yamaguchi, H., Mizuta, T., Kanaseki, T., Komatsu, M., Otsu, K., Tsujimoto, Y., & Shimizu, S. (2009) · Nature · doi:10.1038/nature08455 · Cited by 1,095 · see citing works

NOD2 stimulation induces autophagy in dendritic cells influencing bacterial handling and antigen presentation

Cooney, R. M., BAKER, J. T., Brain, O., Danis, B., Pichulik, T., Allan, P., Ferguson, D. J. P., Campbell, B. J., Jewell, D. P., & Simmons, A. (2009) · Nature Medicine · doi:10.1038/nm.2069 · Cited by 1,046 · see citing works

Microautophagy of Cytosolic Proteins by Late Endosomes

Sahu, R., Kaushik, S., Clement, C. C., Cannizzo, E. S., Scharf, B., Follenzi, A., Potolicchio, I., Nieves, E., Cuervo, A. M., & Santambrogio, L. (2011) · Developmental Cell · doi:10.1016/j.devcel.2010.12.003 · Cited by 902 · see citing works

Chaperone-mediated autophagy: a unique way to enter the lysosome world

Kaushik, S., & Cuervo, A. M. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.05.006 · Cited by 850 · see citing works

Eating Oneself and Uninvited Guests

Levine, B. (2005) · Cell · doi:10.1016/j.cell.2005.01.005 · Cited by 785 · see citing works

A Role for Autophagy in the Extension of Lifespan by Dietary Restriction in C. elegans

Hansen, M., Chandra, A., Mitic, L. L., Onken, B., Driscoll, M., & Kenyon, C. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.0040024 · Cited by 766 · see citing works

Extracellular M. tuberculosis DNA Targets Bacteria for Autophagy by Activating the Host DNA-Sensing Pathway

Watson, R. O., Manzanillo, P. S., & Cox, J. S. (2012) · Cell · doi:10.1016/j.cell.2012.06.040 · Cited by 755 · see citing works

Antigen-loading compartments for major histocompatibility complex class II molecules continuously receive input from autophagosomes.

Schmid, D., Pypaert, M., & Münz, C. (2007) · Immunity · doi:10.1016/j.immuni.2006.10.018 · Cited by 732 · see citing works

Overexpression of Atg5 in mice activates autophagy and extends lifespan

Pyo, J.-O., Yoo, S.-M., Ahn, H.-H., Nah, J., Hong, S.-H., Kam, T.-I., Jung, S., & Jung, Y.-K. (2013) · Nature Communications · doi:10.1038/ncomms3300 · Cited by 721 · see citing works

NLRP6 Inflammasome Orchestrates the Colonic Host-Microbial Interface by Regulating Goblet Cell Mucus Secretion

Wlodarska, M., Thaiss, C. A., Nowarski, R., Henao-Mejia, J., Zhang, J.-P., Brown, E. M., Frankel, G., Levy, M., Katz, M. N., Philbrick, W. M., et al. (2014) · Cell · doi:10.1016/j.cell.2014.01.026 · Cited by 708 · see citing works

Autophagy promotes MHC class II presentation of peptides from intracellular source proteins

Dengjel, J., Schoor, O., Fischer, R., Reich, M. R., Kraus, M., Müller, M., Kreymborg, K., Altenberend, F., Brandenburg, J., Kalbacher, H., et al. (2005) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0501190102 · Cited by 680 · see citing works

Age-related decline in chaperone-mediated autophagy

Cuervo, A. M., & Dice, J. F. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002102200 · Cited by 665 · see citing works

A critical role for the autophagy gene Atg5 in T cell survival and proliferation

Pua, H. H., Dzhagalov, I., Chuck, M., Mizushima, N., & He, Y.-W. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061303 · Cited by 622 · see citing works

Acetylation Targets the M2 Isoform of Pyruvate Kinase for Degradation through Chaperone-Mediated Autophagy and Promotes Tumor Growth

Lv, L., Dong, L., Zhao, D., Lin, R., Chu, Y., Zhang, H., Zha, Z., Liu, Y., Li, Z., Xu, Y., et al. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.04.025 · Cited by 605 · see citing works

Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance

Arndt, V., Dick, N., Tawo, R., Dreiseidler, M., Wenzel, D., Hesse, M., Fürst, D. O., Säftig, P., Saint, R. B., Fleischmann, B. K., et al. (2010) · Current Biology · doi:10.1016/j.cub.2009.11.022 · Cited by 572 · see citing works

Canonical and non-canonical autophagy: variations on a common theme of self-eating?

Codogno, P., Mehrpour, M., & Proikas‐Cezanne, T. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3249 · Cited by 545 · see citing works

Autophagy in thymic epithelium shapes the T-cell repertoire and is essential for tolerance

Nedjic, J., Aichinger, M., Emmerich, J., Mizushima, N., & Klein, L. (2008) · Nature · doi:10.1038/nature07208 · Cited by 533 · see citing works

Consequences of the selective blockage of chaperone-mediated autophagy

Massey, A. C., Kaushik, S., Sovak, G., Kiffin, R., & Cuervo, A. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507436103 · Cited by 529 · see citing works

Restoration of chaperone-mediated autophagy in aging liver improves cellular maintenance and hepatic function

Zhang, C., & Cuervo, A. M. (2008) · Nature Medicine · doi:10.1038/nm.1851 · Cited by 520 · see citing works

In vivo requirement for Atg5 in antigen presentation by dendritic cells

Lee, H. K., Mattei, L. M., Steinberg, B. E., Alberts, P., Lee, Y. H., Chervonsky, A., Mizushima, N., Grinstein, S., & Iwasaki, A. (2010) · Immunity · doi:10.1016/j.immuni.2009.12.006 · Cited by 506 · see citing works

Autophagy enhances the efficacy of BCG vaccine by increasing peptide presentation in mouse dendritic cells

Jagannath, C., Lindsey, D. R., Dhandayuthapani, S., Xu, Y., Hunter, R. L., & Eissa, N. T. (2009) · Nature Medicine · doi:10.1038/nm.1928 · Cited by 486 · see citing works

Eating Oneself and Uninvited GuestsAutophagy-Related Pathways in Cellular Defense

Levine, B. (2005) · Cell · doi:10.1016/s0092-8674(05)00043-7 · Cited by 453 · see citing works

Autophagy protects against active tuberculosis by suppressing bacterial burden and inflammation

Castillo, E. F., Dekonenko, A., Arko‐Mensah, J., Mandell, M. A., Dupont, N., Jiang, S., Delgado-Vargas, M., Timmins, G. S., Bhattacharya, D., Yang, H., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210500109 · Cited by 451 · see citing works

Plasma cells require autophagy for sustainable immunoglobulin production

Pengo, N., Scolari, M., Oliva, L., Milan, E., Mainoldi, F., Raimondi, A., Fagioli, C., Merlini, A., Mariani, E., Pasqualetto, E., et al. (2013) · Nature Immunology · doi:10.1038/ni.2524 · Cited by 427 · see citing works

Autophagy Is Essential for Mitochondrial Clearance in Mature T Lymphocytes

Pua, H. H., Guo, J., Komatsu, M., & He, Y.-W. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0801143 · Cited by 424 · see citing works

Receptor interacting protein kinase 2–mediated mitophagy regulates inflammasome activation during virus infection

Lupfer, C., Thomas, P. G., Anand, P. K., Vogel, P., Milasta, S., Martinez, J., Huang, G., Green, M., Kundu, M., Chi, H., et al. (2013) · Nature Immunology · doi:10.1038/ni.2563 · Cited by 384 · see citing works

The autophagy gene <i>ATG5</i> plays an essential role in B lymphocyte development

Miller, B. C., Zhao, Z., Stephenson, L. M., Cadwell, K., Pua, H. H., Lee, H. K., Mizushima, N., Iwasaki, A., He, Y.-W., Swat, W., et al. (2008) · Autophagy · doi:10.4161/auto.5474 · Cited by 352 · see citing works

Noncanonical Autophagy Is Required for Type I Interferon Secretion in Response to DNA-Immune Complexes

Henault, J., Martinez, J., Riggs, J. M., Tian, J., Mehta, P., Clarke, L., Sasai, M., Latz, E., Brinkmann, M. M., Iwasaki, A., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.09.014 · Cited by 348 · see citing works

Phosphofructokinase deficiency impairs ATP generation, autophagy, and redox balance in rheumatoid arthritis T cells

Yang, Z., Fujii, H., Mohan, S. V., Goronzy, J. J., & Weyand, C. M. (2013) · Journal of Experimental Medicine · doi:10.1084/jem.20130252 · Cited by 334 · see citing works

Lamp-2a facilitates MHC class II presentation of cytoplasmic antigens.

Zhou, D.-L., Li, P., Lin, Y., Lott, J., Hislop, A. D., Canaday, D., Brutkiewicz, R., & Blum, J. (2005) · Immunity · doi:10.1016/j.immuni.2005.03.009 · Cited by 321 · see citing works

Delivery of Cytosolic Components by Autophagic Adaptor Protein p62 Endows Autophagosomes with Unique Antimicrobial Properties

Ponpuak, M., Davis, A. S., Roberts, E. A., Delgado, M. A., Dinkins, C., Zhao, Z., Virgin, H. W., Kyei, G. B., Johansen, T., Vergne, I., et al. (2010) · Immunity · doi:10.1016/j.immuni.2010.02.009 · Cited by 308 · see citing works

Mitochondrial dysfunction and oxidative stress mediate the physiological impairment induced by the disruption of autophagy

Wu, J., Quijano, C., Chen, E., Liu, H., Cao, L., Fergusson, M. M., Rovira, I. I., Gutkind, S., Daniels, M. P., Komatsu, M., et al. (2009) · Aging · doi:10.18632/aging.100038 · Cited by 305 · see citing works

Non‐autophagic roles of autophagy‐related proteins

Subramani, S. E., & Malhotra, V. (2013) · EMBO Reports · doi:10.1038/embor.2012.220 · Cited by 276 · see citing works

Macroautophagy Regulates Energy Metabolism during Effector T Cell Activation

Hubbard, V. M., Valdor, R., Patel, B., Singh, R., Cuervo, A. M., & Macian, F. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000576 · Cited by 275 · see citing works

Autophagy in antigen-presenting cells results in presentation of citrullinated peptides to CD4 T cells

Ireland, J. M., & Unanue, E. (2011) · Journal of Experimental Medicine · doi:10.1084/jem.20110640 · Cited by 249 · see citing works

Peroxisome Degradation by Microautophagy in Pichia pastoris : Identification of Specific Steps and Morphological Intermediates

Sakai, Y., Koller, A. A., Rangell, L. K., Keller, G. A., & Subramani, S. E. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.3.625 · Cited by 244 · see citing works

Vaccine Activation of the Nutrient Sensor GCN2 in Dendritic Cells Enhances Antigen Presentation

Ravindran, R., Khan, N., Nakaya, H. I., Li, S., Loebbermann, J., Maddur, M. S., Park, Y. H., Jones, D. P., Chappert, P., Davoust, J. M., et al. (2013) · Science · doi:10.1126/science.1246829 · Cited by 222 · see citing works

The Mechanism and Physiological Function of Macroautophagy

Klionsky, D. J., & Codogno, P. (2013) · Journal of Innate Immunity · doi:10.1159/000351979 · Cited by 221 · see citing works

Autophagy Regulates Endoplasmic Reticulum Homeostasis and Calcium Mobilization in T Lymphocytes

Jia, W., Pua, H. H., Li, Q.-J., & He, Y.-W. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001822 · Cited by 218 · see citing works

Selective Autophagy of the Adaptor Protein Bcl10 Modulates T Cell Receptor Activation of NF-κB

Paul, S., Kashyap, A. K., Jia, W., He, Y.-W., & Schaefer, B. C. (2012) · Immunity · doi:10.1016/j.immuni.2012.04.008 · Cited by 207 · see citing works

Autophagy Regulates Phagocytosis by Modulating the Expression of Scavenger Receptors

Bonilla, D. L., Bhattacharya, A., Sha, Y., Xu, Y., Xiang, Q., Kan, A., Jagannath, C., Komatsu, M., & Eissa, N. T. (2013) · Immunity · doi:10.1016/j.immuni.2013.08.026 · Cited by 191 · see citing works

Starch-binding domain-containing protein 1 (Stbd1) and glycogen metabolism: Identification of the Atg8 family interacting motif (AIM) in Stbd1 required for interaction with GABARAPL1

Jiang, S., Wells, C. D., & Roach, P. J. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.08.106 · Cited by 184 · see citing works

Canonical autophagy dependent on the class III phosphoinositide-3 kinase Vps34 is required for naive T-cell homeostasis

Willinger, T., & Flavell, R. A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1205305109 · Cited by 183 · see citing works

Beclin 1-Independent Pathway of Damage-Induced Mitophagy and Autophagic Stress: Implications for Neurodegeneration and Cell Death

Chu, C. T., Zhu, J.-H., & Dagda, R. (2007) · Autophagy · doi:10.4161/auto.4625 · Cited by 170 · see citing works

Impaired Autophagy, Defective T Cell Homeostasis, and a Wasting Syndrome in Mice with a T Cell–Specific Deletion of Vps34

Parekh, V. V., Wu, L., Boyd, K. L., Williams, J. A., Gaddy, J. A., Olivares–Villagómez, D., Cover, T. L., Zong, W., Zhang, J., & Kaer, L. V. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202071 · Cited by 165 · see citing works

A novel method for autophagy detection in primary cells: Impaired levels of macroautophagy in immunosenescent T cells

Phadwal, K., Alegre-Abarrategui, J., Watson, A. S., Pike, L., Anbalagan, S., Hammond, E. M., Wade-Martins, R., McMichael, A., Klenerman, P., & Simon, A. K. (2012) · Autophagy · doi:10.4161/auto.18935 · Cited by 155 · see citing works

Macroautophagy substrates are loaded onto MHC class II of medullary thymic epithelial cells for central tolerance

Aichinger, M., Wu, C., Nedjic, J., & Klein, L. (2013) · Journal of Experimental Medicine · doi:10.1084/jem.20122149 · Cited by 151 · see citing works

Age-related changes in the regulation of autophagic proteolysis in rat isolated hepatocytes

Donati, A., Cavallini, G., Paradiso, C., Vittorini, S., Pollera, M., Gori, Z., & Bergamini, E. (2001) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/56.7.b288 · Cited by 110 · see citing works

Up-to-date membrane biogenesis in the autophagosome formation

Hamasaki, M., Shibutani, S., & Yoshimori, T. (2013) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2013.03.004 · Cited by 107 · see citing works

Age-Related Oxidative Stress Compromises Endosomal Proteostasis

Cannizzo, E. S., Clement, C. C., Morozova, K., Valdor, R., Kaushik, S., Almeida, L. N., Follo, C., Sahu, R., Cuervo, A. M., Macian, F., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.06.005 · Cited by 95 · see citing works

Evolution of the immune system in humans from infancy to old age

Simon, A. K., Hollander, G. A., & McMichael, A. (2015) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2014.3085 · Cited by 1,796 · see citing works

Age and Age-Related Diseases: Role of Inflammation Triggers and Cytokines

Rea, I. M., Gibson, D. S., McGilligan, V., McNerlan, S. E., Alexander, H. D., & Ross, O. A. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00586 · Cited by 1,267 · see citing works

Measuring biological aging in humans: a quest

Ferrucci, L., Gonzalez‐Freire, M., Fabbri, E., Simonsick, E., Tanaka, T., Moore, Z., Salimi, S., Sierra, F., & de Cabo, R. (2020) · Aging Cell · doi:10.1111/acel.13080 · Cited by 781 · see citing works

Inflammation, epigenetics, and metabolism converge to cell senescence and ageing: the regulation and intervention

Zhu, X., Chen, Z., Shen, W., Huang, G., Sedivy, J. M., Wang, H., & Ju, Z. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00646-9 · Cited by 410 · see citing works

Autophagy in liver diseases: Time for translation?

Allaire, M., Rautou, P.-E., Codogno, P., & Lotersztajn, S. (2019) · Journal of Hepatology · doi:10.1016/j.jhep.2019.01.026 · Cited by 378 · see citing works

Targeting mitochondrial dysfunction can restore antiviral activity of exhausted HBV-specific CD8 T cells in chronic hepatitis B

Fisicaro, P., Barili, V., Montanini, B., Acerbi, G., Ferracin, M., Guerrieri, F., Salerno, D., Boni, C., Massari, M., Cavallo, M. C., et al. (2017) · Nature Medicine · doi:10.1038/nm.4275 · Cited by 344 · see citing works

Time and the Metrics of Aging

Ferrucci, L., Levine, M. E., Kuo, P.-L., & Simonsick, E. M. (2018) · Circulation Research · doi:10.1161/circresaha.118.312816 · Cited by 303 · see citing works

Aging, inflammation, immunity and periodontal disease

Ebersole, J. L., Graves, C. L., González, O. A., Dawson, D. R., Morford, L. A., Emecen‐Huja, P., Hartsfield, J. K., Huja, S. S., Pandruvada, S. N. M., & Wallet, S. M. (2016) · Periodontology 2000 · doi:10.1111/prd.12135 · Cited by 308 · see citing works

The crucial impact of lysosomes in aging and longevity

Carmona‐Gutiérrez, D., Hughes, A. L., Madeo, F., & Ruckenstuhl, C. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.04.009 · Cited by 244 · see citing works

Autophagy and aging: Maintaining the proteome through exercise and caloric restriction

Escobar, K. A., Cole, N. H., Mermier, C. M., & VanDusseldorp, T. A. (2018) · Aging Cell · doi:10.1111/acel.12876 · Cited by 226 · see citing works

Metabolic Alterations in Aging Macrophages: Ingredients for Inflammaging?

van Beek, A. A., Van den Bossche, J., Mastroberardino, P. G., de Winther, M. P. J., & Leenen, P. J. M. (2019) · Trends in Immunology · doi:10.1016/j.it.2018.12.007 · Cited by 207 · see citing works

Immunosenescence: A systems-level overview of immune cell biology and strategies for improving vaccine responses

Crooke, S. N., Ovsyannikova, I. G., Poland, G. A., & Kennedy, R. B. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2019.110632 · Cited by 143 · see citing works

The complex relationships between microglia, alpha-synuclein, and LRRK2 in Parkinson's disease

Schapansky, J., Nardozzi, J. D., & LaVoie, M. J. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2014.09.049 · Cited by 132 · see citing works

The immuno-oncological challenge of COVID-19

Derosa, L., Melenotte, C., Griscelli, F., Gachot, B., Marabelle, A., Kroemer, G., & Zitvogel, L. (2020) · Nature Cancer · doi:10.1038/s43018-020-00122-3 · Cited by 133 · see citing works

Proteostatic and Metabolic Control of Stemness

García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.04.011 · Cited by 123 · see citing works

Autophagy in Age-Associated Neurodegeneration

Metaxakis, A., Ploumi, C., & Tavernarakis, N. (2018) · Cells · doi:10.3390/cells7050037 · Cited by 121 · see citing works

Mitochondrial Function and Mitophagy in the Elderly: Effects of Exercise

Moreira, O. C., Estébanez, B., Martínez‐Flórez, S., Fernández, J. A. D. P., Cuevas, M. J., & González‐Gallego, J. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/2012798 · Cited by 120 · see citing works

Age-associated changes in human CD4+ T cells point to mitochondrial dysfunction consequent to impaired autophagy

Bektas, A., Schurman, S. H., Gonzalez-Freire, M., Dunn, C. A., Singh, A. K., Macian, F., Cuervo, A. M., Sen, R., & Ferrucci, L. (2019) · Aging · doi:10.18632/aging.102438 · Cited by 116 · see citing works

Strategies for late phase preclinical and early clinical trials of senolytics

Gerdes, E. O. W., Misra, A., Espíndola‐Netto, J. M., Tchkonia, T., & Kirkland, J. L. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111591 · Cited by 101 · see citing works

COVID-19 and Crosstalk With the Hallmarks of Aging

Salimi, S., & Hamlyn, J. M. (2020) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaa149 · Cited by 95 · see citing works

Macroautophagy and aging: The impact of cellular recycling on health and longevity

Nieto-Torres, J. L., & Hansen, M. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.101020 · Cited by 91 · see citing works

Biological ageing with HIV infection: evaluating the geroscience hypothesis

Montano, M. A., Oursler, K. K., Xu, K., Sun, Y. V., & Marconi, V. C. (2022) · The Lancet Healthy Longevity · doi:10.1016/s2666-7568(21)00278-6 · Cited by 89 · see citing works

Age and Periodontal Health—Immunological View

Ebersole, J. L., Dawson, D. R., Emecen‐Huja, P., Pandruvada, S. N. M., Basu, A., Nguyen, L., Zhang, Y., & González, O. A. (2018) · Current Oral Health Reports · doi:10.1007/s40496-018-0202-2 · Cited by 84 · see citing works

The Emerging Role of Sestrin2 in Cell Metabolism, and Cardiovascular and Age-Related Diseases

Wanqing, S., Wang, Y., Yang, Z., & Quan, N. (2020) · Aging and Disease · doi:10.14336/ad.2019.0320 · Cited by 80 · see citing works

Key roles of autophagy in regulating T‐cell function

Botbol, Y. M., Guerrero‐Ros, I., & Macián, F. (2016) · European Journal of Immunology · doi:10.1002/eji.201545955 · Cited by 78 · see citing works

Autophagy, EVs, and Infections: A Perfect Question for a Perfect Time

Pleet, M. L., Branscome, H., DeMarino, C., Pinto, D. O., Zadeh, M. A., Rodriguez, M., Sariyer, I. K., El‐Hage, N., & Kashanchi, F. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00362 · Cited by 71 · see citing works

Biological and Functional Biomarkers of Aging: Definition, Characteristics, and How They Can Impact Everyday Cancer Treatment

Colloca, G. A., Capua, B. D., Bellieni, A., Fusco, D., Ciciarello, F., Tagliaferri, L., Valentini, V., & Balducci, L. (2020) · Current Oncology Reports · doi:10.1007/s11912-020-00977-w · Cited by 77 · see citing works

Physical Exercise, a Potential Non-Pharmacological Intervention for Attenuating Neuroinflammation and Cognitive Decline in Alzheimer’s Disease Patients

Ribarič, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063245 · Cited by 72 · see citing works

Effects of aerobic training on markers of autophagy in the elderly

Mejías-Peña, Y., Rodriguez-Miguelez, P., Fernandez-Gonzalo, R., Martínez-Flórez, S., Almar, M., de Paz, J. A., Cuevas, M. J., & González-Gallego, J. (2016) · AGE · doi:10.1007/s11357-016-9897-y · Cited by 69 · see citing works

Autophagy in T Cell Function and Aging

Macián, F. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00213 · Cited by 69 · see citing works

Manipulating Autophagic Processes in Autoimmune Diseases: A Special Focus on Modulating Chaperone-Mediated Autophagy, an Emerging Therapeutic Target

Wang, F., & Muller, S. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00252 · Cited by 67 · see citing works

Effects of Physical Exercise on Autophagy and Apoptosis in Aged Brain: Human and Animal Studies

Andreotti, D., Silva, J. N., Matumoto, A. M., Orellana, A., Mello, P. S. D., & Kawamoto, E. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.00094 · Cited by 56 · see citing works

CISH impairs lysosomal function in activated T cells resulting in mitochondrial DNA release and inflammaging

Jin, J., Mu, Y., Zhang, H., Sturmlechner, I., Wang, C., Jadhav, R. R., Xia, Q., Weyand, C. M., & Goronzy, J. J. (2023) · Nature Aging · doi:10.1038/s43587-023-00399-w · Cited by 65 · see citing works

Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality

Scherag, A., Schöneweck, F., Kesselmeier, M., Taudien, S., Platzer, M., Felder, M., Sponholz, C., Rautanen, A., Hill, A. V. S., Hinds, C., et al. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.08.043 · Cited by 64 · see citing works

Autophagy as a Therapeutic Target to Enhance Aged Muscle Regeneration

Lee, D. E., Bareja, A., Bartlett, D. B., & White, J. P. (2019) · Cells · doi:10.3390/cells8020183 · Cited by 64 · see citing works

Autophagy in liver diseases

Kouroumalis, E., Voumvouraki, A., Augoustaki, A., & Samonakis, D. N. (2021) · World Journal of Hepatology · doi:10.4254/wjh.v13.i1.6 · Cited by 64 · see citing works

Activation-Induced Autophagy Is Preserved in CD4+ T-Cells in Familial Longevity

Raz, Y., Guerrero‐Ros, I., Maier, A. B., Slagboom, P. E., Atzmon, G., Barzilai, N., & Macián, F. (2017) · The Journals of Gerontology Series A · doi:10.1093/gerona/glx020 · Cited by 63 · see citing works

Integrating Environment and Aging Research: Opportunities for Synergy and Acceleration

Malecki, K. M. C., Andersen, J. K., Geller, A. M., Harry, G. J., Jackson, C. L., James, K. A., Miller, G. W., & Ottinger, M. A. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.824921 · Cited by 61 · see citing works

Myalgia and chronic fatigue syndrome following immunization: macrophagic myofasciitis and animal studies support linkage to aluminum adjuvant persistency and diffusion in the immune system

Gherardi, R. K., Crépeaux, G., & Authier, F. (2019) · Autoimmunity Reviews · doi:10.1016/j.autrev.2019.05.006 · Cited by 61 · see citing works

The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy

Aragonès, G., Rowan, S., Francisco, S. G., Whitcomb, E. A., Yang, W., Perini-Villanueva, G., Schalkwijk, C. G., Taylor, A., & Bejarano, E. (2021) · Cells · doi:10.3390/cells10081852 · Cited by 51 · see citing works

Ginseng gintonin, aging societies, and geriatric brain diseases

Choi, S.-H., Lee, R., Nam, S. M., Kim, D.-G., Cho, I., Kim, H., Cho, Y., Rhim, H., & Nah, S.-Y. (2020) · Integrative Medicine Research · doi:10.1016/j.imr.2020.100450 · Cited by 51 · see citing works

Treatment delay and fatal outcomes of pulmonary tuberculosis in advanced age: a retrospective nationwide cohort study

Lee, C., Wang, J., Lin, H.-C., Lin, P.-Y., Chang, J., Suk, C., Lee, L., Lan, C., & Bai, K. (2017) · BMC Infectious Diseases · doi:10.1186/s12879-017-2554-y · Cited by 51 · see citing works

The melting pot of the MHC II peptidome

Stern, L. J., & Santambrogio, L. (2016) · Current Opinion in Immunology · doi:10.1016/j.coi.2016.03.004 · Cited by 45 · see citing works

Orchestrating the network of molecular pathways affecting aging: Role of nonselective autophagy and mitophagy

Knuppertz, L., & Osiewacz, H. D. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.01.003 · Cited by 44 · see citing works

Reduced mitophagy in the cochlea of aged C57BL/6J mice

Oh, J., Youn, C. K., Jun, Y., Jo, E.-R., & Cho, S. I. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.110946 · Cited by 43 · see citing works

Maximizing Longevity and Healthspan: Multiple Approaches All Converging on Autophagy

Bareja, A., Lee, D. E., & White, J. P. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00183 · Cited by 41 · see citing works

Dendritic Polyglycerol Sulfates in the Prevention of Synaptic Loss and Mechanism of Action on Glia

Maysinger, D., Ji, J. X., Moquin, A., Hossain, S., Hancock, M. A., Zhang, I., Chang, P. K. ‐., Rigby, M., Anthonisen, M., Grütter, P., et al. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00301 · Cited by 37 · see citing works

The aged liver: Beyond cellular senescence

Allaire, M., & Gilgenkrantz, H. (2019) · Clinics and Research in Hepatology and Gastroenterology · doi:10.1016/j.clinre.2019.07.011 · Cited by 36 · see citing works

The Vici syndrome protein EPG5 regulates intracellular nucleic acid trafficking linking autophagy to innate and adaptive immunity

Mortari, E. P., Folgiero, V., Marcellini, V., Romania, P., Bellacchio, E., D’Alicandro, V., Bocci, C., Carrozzo, R., Martinelli, D., Petrini, S., et al. (2017) · Autophagy · doi:10.1080/15548627.2017.1389356 · Cited by 35 · see citing works

miR-142 induces accumulation of reactive oxygen species (ROS) by inhibiting pexophagy in aged bone marrow mesenchymal stem cells

Houri, K., Mori, T., Onodera, Y., Tsujimoto, T., Takehara, T., Nakao, S., Teramura, T., & Fukuda, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-60346-2 · Cited by 36 · see citing works

Cell Death and Skin Disease

Harberts, E. M., Heitmiller, K., & Gaspari, A. A. (2017) · Springer eBooks · doi:10.1007/978-3-319-29785-9_13 · Cited by 33 · see citing works

Targeting Autophagy in Obesity‐Associated Heart Disease

Castañeda, D., Gabani, M. H., Choi, S. K., Nguyen, Q. M., Chen, C., Mapara, A., Kassan, A., González, A. A., Ait‐Aissa, K., & Kassan, M. (2019) · Obesity · doi:10.1002/oby.22455 · Cited by 31 · see citing works

Humanin-induced autophagy plays important roles in skeletal muscle function and lifespan extension

Kim, S.-J., Devgan, A., Miller, B., Lee, S. M., Kumagai, H., Wilson, K. A., Wassef, G., Wong, R., Mehta, H. H., Cohen, P., et al. (2022) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2021.130017 · Cited by 30 · see citing works

The Interplay between Immunosenescence and Microbiota in the Efficacy of Vaccines

Cianci, R., Franza, L., Massaro, M. G., Borriello, R., Vito, F., & Gambassi, G. (2020) · Vaccines · doi:10.3390/vaccines8040636 · Cited by 31 · see citing works

Regulation of autophagy as a therapy for immunosenescence‐driven cancer and neurodegenerative diseases: The role of exercise

Batatinha, H., Diniz, T. A., Teixeira, A. A. D. S., Krüger, K., & Neto, J. C. R. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28318 · Cited by 29 · see citing works

Human cells involved in atherosclerosis have a sex

Franconi, F., Rosano, G. M. C., Basili, S., Montella, A., & Campesi, I. (2016) · International Journal of Cardiology · doi:10.1016/j.ijcard.2016.11.118 · Cited by 28 · see citing works

Role of autophagy in the pathogenesis of Alzheimer disease

Kızılarslanoğlu, M. C., & Ülger, Z. (2015) · TURKISH JOURNAL OF MEDICAL SCIENCES · doi:10.3906/sag-1407-75 · Cited by 24 · see citing works

Adenosine 5′-monophosphate-activated protein kinase ameliorates bovine adipocyte oxidative stress by inducing antioxidant responses and autophagy

Xu, Q., Fan, Y., Loor, J. J., Liang, Y., Sun, X., Jia, H., Zhao, C., & Xu, C. (2021) · Journal of Dairy Science · doi:10.3168/jds.2020-18728 · Cited by 23 · see citing works

The Mitochondrion-lysosome Axis in Adaptive and Innate Immunity: Effect of Lupus Regulator Peptide P140 on Mitochondria Autophagy and NETosis

Bendorius, M., Neeli, I., Wang, F., Bonam, S. R., Dombi, E., Buron, N., Borgne‐Sanchez, A., Poulton, J., Radic, M. Z., & Muller, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02158 · Cited by 23 · see citing works

Inhaled Corticosteroids Increase the Risk of Pneumonia in Patients With Chronic Obstructive Pulmonary Disease

Lee, M., Lee, C., Chien, S., Chang, J., She, H.-L., Wang, J., & Yu, M.-C. (2015) · Medicine · doi:10.1097/md.0000000000001723 · Cited by 22 · see citing works

New mechanisms driving muscle stem cell regenerative decline with aging

Sousa‐Victor, P., García‐Prat, L., & Muñoz‐Cánoves, P. (2018) · The International Journal of Developmental Biology · doi:10.1387/ijdb.180041pm · Cited by 22 · see citing works

Proteodynamics in aging human T cells – The need for its comprehensive study to understand the fine regulation of T lymphocyte functions

Witkowski, J. M., Mikosik, A., Bryl, E., & Fülöp, T. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.10.009 · Cited by 22 · see citing works

Age-associated reduction in ER-Mitochondrial contacts impairs mitochondrial lipid metabolism and autophagosome formation in the heart

Hong, W., Zeng, X., Ma, R., Tian, Y., Miu, H., Ran, X., Song, R., Luo, Z., Ju, D., Ma, D., et al. (2025) · Cell Death and Differentiation · doi:10.1038/s41418-025-01511-w · Cited by 21 · see citing works

“Reframing” dopamine signaling at the intersection of glial networks in the aged Parkinsonian brain as innate Nrf2/Wnt driver: Therapeutical implications

Marchetti, B., Giachino, C., Tirolo, C., & Serapide, M. F. (2022) · Aging Cell · doi:10.1111/acel.13575 · Cited by 22 · see citing works

Autophagic response to exercise in peripheral blood mononuclear cells from young men is intensity-dependent and is altered by exposure to environmental heat

McCormick, J. J., Côté, M. D., King, K. E., McManus, M. K., Goulet, N., Dokładny, K., Moseley, P. L., & Kenny, G. P. (2022) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00110.2022 · Cited by 21 · see citing works

HMGB1-induced autophagy in Schwann cells promotes neuroblastoma proliferation.

Liu, Y., & Song, L. (2015) · Europe PMC (PubMed Central) · Cited by 20 · see citing works

Food Antioxidants and Aging: Theory, Current Evidence and Perspectives

Miyazawa, T., Abe, C., Burdeos, G. C., Matsumoto, A., & Toda, M. (2022) · Nutraceuticals · doi:10.3390/nutraceuticals2030014 · Cited by 19 · see citing works

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 · see citing works

The interplay between physical exercise and autophagy signaling in brain health, neurodegenerative diseases and aging

Gao, B., Wang, L., Gong, J., Zhu, Z., Liu, Q., Han, Y., & Wang, H. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1579208 · Cited by 16 · see citing works

A Review of the Potential Effects of Melatonin in Compromised Mitochondrial Redox Activities in Elderly Patients With COVID-19

Su, W., Wu, C., Wu, S. V., Lee, M., Liao, M.-T., Lu, K., & Lu, C. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.865321 · Cited by 17 · see citing works

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 · see citing works

Hydroxychloroquine can potentially interfere with immune function in COVID-19 patients: Mechanisms and insights

Devarajan, A., & Vaseghi, M. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101810 · Cited by 17 · see citing works

The intensity-dependent effects of exercise and superimposing environmental heat stress on autophagy in peripheral blood mononuclear cells from older men

McCormick, J. J., McManus, M. K., King, K. E., Goulet, N., & Kenny, G. P. (2023) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00163.2023 · Cited by 16 · see citing works

Perturbation of bulk and selective macroautophagy, abnormal UPR activation and their interplay pave the way to immune dysfunction, cancerogenesis and neurodegeneration in ageing

Cirone, M. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101026 · Cited by 15 · see citing works

Autophagy and Glycative Stress: A Bittersweet Relationship in Neurodegeneration

Gómez, O., Perini-Villanueva, G., Yuste, A., Rodríguez‐Navarro, J. A., Poch, E., & Bejarano, E. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.790479 · Cited by 14 · see citing works

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 · see citing works

Endoplasmic Reticulum Stress in Elderly Patients with COVID-19: Potential of Melatonin Treatment

Yiang, G.-T., Wu, C.-C., Lu, C.-L., Hu, W.-C., Tsai, Y., Huang, Y.-M., Su, W.-L., & Lu, K.-C. (2023) · Viruses · doi:10.3390/v15010156 · Cited by 11 · see citing works

Mitochondrial DNA copy number and telomere length in peripheral blood mononuclear cells in comparison with whole blood in three different age groups

Zole, E., & Ranka, R. (2019) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2019.04.007 · Cited by 11 · see citing works

The Role of Autophagy in Aging

Markaki, M., Metaxakis, A., & Tavernarakis, N. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00002-0 · Cited by 7 · see citing works

Inflammatory Molecular Mediators and Pathways Involved in Vascular Aging and Stroke: A Comprehensive Review

Soliman, A. M., Das, S., & Mahakkanukrauh, P. (2021) · Current Medicinal Chemistry · doi:10.2174/0929867328666210901122359 · Cited by 5 · see citing works

Microglial Dysfunction in Brain Aging and Neurodegeneration

Marschallinger, J., Mosher, K. I., & Wyss‐Coray, T. (2017) · Springer eBooks · doi:10.1007/978-3-319-64597-1_149-1 · Cited by 4 · see citing works

Autophagy in Inflammation: the p38α MAPK-ULK1 Axis

She, H., He, Y., Zhao, Y., & Mao, Z. (2018) · Macrophage · doi:10.14800/macrophage.1629 · Cited by 4 · see citing works

Potential of nanoparticles and nanopolymers in treatment of age-associated diseases

Saadatpour, F., Mohammadipanah, F., Zohourian, N., & Hodjat, M. (2021) · Advances in Natural Sciences Nanoscience and Nanotechnology · doi:10.1088/2043-6262/ac42c7 · Cited by 3 · see citing works

Lower Beclin-1 mRNA Levels in Pediatric Compared With Adult Patients With Otitis Media With Effusion

Hoon, K. S., Gu, K. M., Shim, H. S., Su, K. S., Il, K. Y., & Geun, Y. S. (2018) · The Journal of International Advanced Otology · doi:10.5152/iao.2018.4481 · Cited by 4 · see citing works

Trends and delays in pulmonary tuberculosis diagnosis among elderly patients (≥ 60 Years) in Southern China: a 13-year surveillance data analysis (2010–2022)

Zhou, F., Sun, Q., Huang, S., Li, J., Chen, Y., & Feng, H. (2025) · BMC Public Health · doi:10.1186/s12889-025-23031-5 · Cited by 3 · see citing works

Mitophagy Decreases in the Peripheral Vestibular System of Aged C57BL/6J Mice

Cho, S. I., Jo, E.-R., & Lee, S. M. (2023) · In Vivo · doi:10.21873/invivo.13426 · Cited by 3 · see citing works

Integrative analysis of methylation and transcriptional profiles to predict aging and construct aging specific cross-tissue networks

Wang, Y., Huang, T., Xie, L., & Liu, L. (2016) · BMC Systems Biology · doi:10.1186/s12918-016-0354-4 · Cited by 3 · see citing works

A Geroscience Approach to Preventing Pathologic Consequences of COVID-19

Dou, Y., Fatemi, S., Darvas, M., Gale, M., & Ladiges, W. (2020) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2020.29018.dou · Cited by 3 · see citing works

Immunosenescence and infectious diseases

Moutschen, M. P., Martens, H., & Geenen, V. G. (2017) · doi:10.1093/med/9780198701590.003.0079 · Cited by 2 · see citing works

Autophagy

Cuervo, A. M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00220-0 · Cited by 2 · see citing works

Target Autophagy as a Novel Therapeutic Strategy in Autoimmune Diseases

Wilhelm, M., & Muller, S. (2016) · Springer eBooks · doi:10.1007/978-3-319-30079-5_13 · Cited by 1 · see citing works

Age-Related Changes in Immune Regulation by Noncoding RNAs

Wang, W., Qian, F., & Montgomery, R. R. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_109 · Cited by 1 · see citing works

Sestryny jako modulatory procesów starzenia i chorób związanych z wiekiem*

Gabryel, B., & Duszkiewicz, R. (2021) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/01.3001.0014.9471 · Cited by 1 · see citing works

Microglial Dysfunction in Brain Aging and Neurodegeneration

Marschallinger, J., Mosher, K. I., & Wyss‐Coray, T. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_149 · Cited by 1 · see citing works

“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 1 · see citing works

Protein Degradation and the Lysosomal System

Kaushik, S., & Cuervo, A. M. (2020) · Wiley eBooks · doi:10.1002/9781119436812.ch11 · Cited by 1 · see citing works

Autophagy

Cuervo, A. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.30054-2 · Cited by 1 · see citing works

Ultrastructural changes of lymphocytes in patients with schizophrenia treated with olanzapine

Бонарцев, П. Д., Рахманова, В. И., & Uranova, N. A. (2016) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro20161163149-54

The aging immune system and nutritional interventions

van Beek, A. A. (2017) · doi:10.18174/392235

Autophagy and T Cell Aging

Macián, F. (2018) · Springer eBooks · doi:10.1007/978-3-319-64597-1_112-1

Autophagy in Immunity and Cell-Autonomous Defense Against

Microbes, I., & Deretic, V. P. (2015)

Autophagy in immunity and cell‐autonomous defense against intracellular microbes

Deretic, V. P. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00995.x · Cited by 363 · see citing works

Autophagy in the immune system

Vávra, D. (2011) · Digital Repository (National Repository of Grey Literature)

Autophagy and autophagy-related proteins in the immune system

Shibutani, S., Saitoh, T., Nowag, H., Münz, C., & Yoshimori, T. (2015) · Nature Immunology · doi:10.1038/ni.3273 · Cited by 581 · see citing works

Autophagy as an immune defense mechanism.

Deretic, V. (2006) · Current Opinion in Immunology · doi:10.1016/j.coi.2006.05.019 · Cited by 208 · see citing works