The autophagy initiating kinase ULK1 is regulated via opposing phosphorylation by AMPK and mTOR

AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1

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Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy

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Atg1 phosphorylation is activated by AMPK and indispensable for autophagy induction in insects

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Autophagy: a necessary evil in cancer and inflammation

Mathur, A., Ritu, R., Chandra, P., & Das, A. (2024) · 3 Biotech · doi:10.1007/s13205-023-03864-w · Cited by 16

Aberrant STING activation promotes macrophage senescence by suppressing autophagy in vascular aging from diabetes

Ding, H., Zhang, Q., Yang, R., Fu, L., Jiang, H., Zhu, Q., & Tai, S. (2024) · iScience · doi:10.1016/j.isci.2024.111594 · Cited by 17

Ras transformation uncouples the kinesin-coordinated cellular nutrient response

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Metformin alleviates β‑glycerophosphate‑induced calcification of vascular smooth muscle cells via AMPK/mTOR‑activated autophagy

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C. elegans to model autophagy-related human disorders

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Intensity, Duration, and Context Dependency of the Responses to Nutrient Surplus and Deprivation Signaling in the Heart: Insights Into the Complexities of Cardioprotection

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Mechanism of autophagy induced by low concentrations of chlorantraniliprole in silk gland, Bombyx mori

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Metformin and bladder cancer: Drug repurposing as a potential tool for novel therapy: A review

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The energy sensing LKB 1– AMPK α1 pathway regulates IGF 1 secretion and consequent activation of the IGF 1R– PKB pathway in primary hepatocytes

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Increased autophagy signaling but not proteasome activity in human skeletal muscle after prolonged low‐intensity exercise with negative energy balance

Moberg, M., Hendo, G., Jakobsson, M., Mattsson, C. M., Ekblom‐Bak, E., Flockhart, M., Pontén, M., Söderlund, K., & Ekblom, B. T. (2017) · Physiological Reports · doi:10.14814/phy2.13518 · Cited by 14

Simultaneous loss of TSC1 and DEPDC5 in skeletal and cardiac muscles produces early-onset myopathy and cardiac dysfunction associated with oxidative damage and SQSTM1/p62 accumulation

Cho, C., Kim, Y., Park, S.-R., Kim, B. Y., Davis, C. S., Hwang, I., Brooks, S. V., Lee, J. H., & Kim, M. (2021) · Autophagy · doi:10.1080/15548627.2021.2016255 · Cited by 13

Using Intermittent Fasting as a Non-pharmacological Strategy to Alleviate Obesity-Induced Hypothalamic Molecular Pathway Disruption

Oliveira, L. D. C., Morais, G. P., Ropelle, E. R., de Moura, L. P., Cintra, D. E., Pauli, J. R., de Freitas, E. C., Rorato, R. C., & da Silva, A. S. R. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.858320 · Cited by 17

Cannabis smoke condensate induces human gingival epithelial cell damage through apoptosis, autophagy, and oxidative stress

Tazi, N., Semlali, A., Loubaki, L., Alamri, A. M., & Rouabhia, M. (2022) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2022.105498 · Cited by 13

Advances in nanotherapeutic strategies for Huntington's disease: Design, delivery, and neuroprotective mechanisms

Khan, S., Bano, N., Ahamad, S., Dar, N. J., Nazir, A., & Bhat, S. A. (2024) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2024.216206 · Cited by 14

Period 2 -Induced Activation of Autophagy Improves Cardiac Remodeling After Myocardial Infarction

Zhang, X., Wang, L., Yan, W., Lu, X., Li, X., & Sun, Y. (2019) · Human Gene Therapy · doi:10.1089/hum.2019.146 · Cited by 12

mTORC1 restricts hepatitis C virus RNA replication through ULK1-mediated suppression of miR-122 and facilitates post-replication events

Johri, M. K., Lashkari, H. V., Gupta, D., Vedagiri, D., & Harshan, K. H. (2019) · Journal of General Virology · doi:10.1099/jgv.0.001356 · Cited by 13

Updates from the Intestinal Front Line: Autophagic Weapons against Inflammation and Cancer

Madia, F., Grossi, V., Peserico, A., & Simone, C. (2012) · Cells · doi:10.3390/cells1030535 · Cited by 13

Nano-zinc oxide (nZnO) targets the AMPK-ULK1 pathway to promote bone regeneration

Chen, X., Weng, Z., Zhang, H., Jiao, J., Liang, J., Xu, J., Wang, D., Liu, Q., Yan, Q., & Gu, A. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04322-5 · Cited by 12

Depletion of p18/LAMTOR1 promotes cell survival via activation of p27kip1‐dependent autophagy under starvation

Zada, S., Noh, H. S., Baek, S. M., Ha, J. H., Hahm, J. R., & Kim, D. R. (2015) · Cell Biology International · doi:10.1002/cbin.10497 · Cited by 12

Deliberation on debilitating condition of cancer cachexia: Skeletal muscle wasting

Dave, S., & Patel, B. M. (2023) · Fundamental and Clinical Pharmacology · doi:10.1111/fcp.12931 · Cited by 12

Caprin-1 influences autophagy-induced tumor growth and immune modulation in pancreatic cancer

Yang, W., Chen, H., Li, G., Zhang, T., Sui, Y., Liu, L., Hu, J., Wang, G., Chen, H., Wang, Y., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04693-4 · Cited by 12

Multifaceted role of SMCR8 as autophagy regulator

Jung, J., & Behrends, C. (2017) · Small GTPases · doi:10.1080/21541248.2017.1346553 · Cited by 13

AMPKα promotes basal autophagy induction in Dictyostelium discoideum

Maurya, R., Kumar, R., & Saran, S. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.29373 · Cited by 12

β-guanidinopropionic acid and metformin differentially impact autophagy, mitochondria and cellular morphology in developing C2C12 muscle cells

Crocker, C. L., Baumgarner, B. L., & Kinsey, S. T. (2019) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-019-09568-0 · Cited by 13

Mineral trioxide aggregate‐induced AMPK activation stimulates odontoblastic differentiation of human dental pulp cells

Kim, Y., Kim, W., Bae, S., Yang, S., Park, S., Kim, S., & Jung, J. (2020) · International Endodontic Journal · doi:10.1111/iej.13460 · Cited by 12

A bibliometric analysis of myocardial ischemia/reperfusion injury from 2000 to 2023

Wang, Y., Guo, L., Zhang, Z., Fu, S., Huang, P., Wang, A., Liu, M., & Ma, X. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1180792 · Cited by 12

How to explain exercise-induced phenotype from molecular data: rethink and reconstruction based on AMPK and mTOR signaling

Qi, Z., Zhai, X., & Ding, S. (2013) · SpringerPlus · doi:10.1186/2193-1801-2-693 · Cited by 12

Autophagy and cancer

Schüller, H. E. K., & Gözüaçık, D. (2014) · TURKISH JOURNAL OF BIOLOGY · doi:10.3906/biy-1408-16 · Cited by 13

Disulfide Cleavage in a Dimeric Epipolythiodioxopiperazine Natural Product Diminishes Its Apoptosis-Inducing Effect but Enhances Autophagy in Tumor Cells

Li, E., Hou, B., Gao, Q., Yang, X., Zhang, C., Liu, X., Jiang, X., & Che, Y. (2020) · Journal of Natural Products · doi:10.1021/acs.jnatprod.9b00994 · Cited by 12

Programmed Cell Death in the Left and Right Ventricle of the Late Phase of Post-Infarction Heart Failure

Lichý, M., Szobi, A., Hrdlička, J., Neckář, J., Kolář, F., & Adameová, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207782 · Cited by 11

MAP3K11 facilitates autophagy activity and is correlated with malignancy of oral squamous cell carcinoma

Liu, P., Chen, H.-C., Ger, L., Tsai, W., Tseng, H., Lee, C., Yang, W., & Shu, C. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30881 · Cited by 12

Stefin B Inhibits NLRP3 Inflammasome Activation via AMPK/mTOR Signalling

Prebanda, M. T., Biasizzo, M., Dolinar, K., Pirkmajer, S., Turk, B., Brault, V., Hérault, Y., & Kopitar‐Jerala, N. (2023) · Cells · doi:10.3390/cells12232731 · Cited by 11

Roles of Autophagy and Oxidative Stress in Cardiovascular Disease

Yun, H. R., Singh, M. K., Han, S., Ranbhise, J. S., Ha, J., Kim, S. S., & Kang, I. (2025) · Antioxidants · doi:10.3390/antiox14101263 · Cited by 13

Mitophagy: At the heart of mitochondrial quality control in cardiac aging and frailty

Picca, A., Calvani, R., Coelho‐Júnior, H. J., & Marzetti, E. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2021.111508 · Cited by 11

Rapalogs induce non‐apoptotic, autophagy‐dependent cell death in HPV‐negative TP53 mutant head and neck squamous cell carcinoma

Alam, M. M., Fermin, J. M., Spiller, P. T., Burnett, C., Rong, X., Moore‐Medlin, T., Maxwell, C. O., Khandelwal, A. R., & Nathan, C. O. (2021) · Molecular Carcinogenesis · doi:10.1002/mc.23357 · Cited by 12

Novel insights into exhaustive exercise-induced myocardial injury: Focusing on mitochondrial quality control

Shi, M., Dong, Z., Zhao, K., He, X., Sun, Y., Ren, J. T., & Ge, W. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.1015639 · Cited by 12

The role of the HORMA domain proteins ATG13 and ATG101 in initiating autophagosome biogenesis

Nguyen, A., & Faesen, A. C. (2023) · FEBS Letters · doi:10.1002/1873-3468.14717 · Cited by 11

Intermittent Fasting to the Eye: A New Dimension Involved in Physiological and Pathological Changes

Feng, J., Zhang, S., Li, W., Bai, T., Liu, Y., & Chang, X. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.867624 · Cited by 11

Small molecule H89 renders the phosphorylation of S6K1 and AKT resistant to mTOR inhibitors

Melick, C. H., & Jewell, J. L. (2020) · Biochemical Journal · doi:10.1042/bcj20190958 · Cited by 13

Lipid-based DNA/siRNA transfection agents disrupt neuronal bioenergetics and mitophagy

Napoli, E., Liu, S., Marsilio, I., Zarbalis, K., & Giulivi, C. (2017) · Biochemical Journal · doi:10.1042/bcj20170632 · Cited by 12

Somatic Growth and Maturation

Cuttler, L., Misra, M., & Koontz, M. B. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-18907-1.00022-6 · Cited by 11

Iditarod , a Drosophila homolog of the Irisin precursor FNDC5 , is critical for exercise performance and cardiac autophagy

Cobb, T., Hwang, I., Soukar, M., Namkoong, S., Cho, U., Safdar, M., Kim, M., Wessells, R. J., & Lee, J. H. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2220556120 · Cited by 10

Beclin1 Deficiency Suppresses Epileptic Seizures

Yang, M., Lin, P., Jing, W., Guo, H., Chen, H., Chen, Y., Guo, Y., Gu, Y., He, M., Wu, J., et al. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.807671 · Cited by 9

Phosphorylation of the novel mTOR substrate Unkempt regulates cellular morphogenesis

Baskaran, P., Mihaylov, S. R., Vinsland, E., Shah, K., Granat, L., Ultanir, S. K., Tee, A. R., Murn, J., & Bateman, J. M. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102788 · Cited by 10

Autophagy: ‘Self-Eating’ Your Way to Longevity

Pattison, C. J., & Korolchuk, V. I. (2018) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-981-13-2835-0_2 · Cited by 10

Chronic Restraint Stress-Induced Muscle Atrophy Leads to Fatigue in Mice by Inhibiting the AMPK Signaling Pathway

Wang, Z., Xia, T., Jin, S., Liu, X., Pan, R., Yan, M., & Chang, Q. (2021) · Biomedicines · doi:10.3390/biomedicines9101321 · Cited by 10

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 10

Rapamycin improves satellite cells’ autophagy and muscle regeneration during hypercapnia

Balnis, J., Jackson, E. L., Drake, L. A., Singer, D. V., Ramos, R. B., Singer, H. A., & Jaitovich, A. (2024) · JCI Insight · doi:10.1172/jci.insight.182842 · Cited by 10

The multifaceted roles of nucleophagy in cancer development and therapy

Zhao, L., Li, W., Luo, X., & Sheng, S. (2020) · Cell Biology International · doi:10.1002/cbin.11504 · Cited by 9

6-Methyl flavone inhibits Nogo-B expression and improves high fructose diet-induced liver injury in mice

Gong, K., Zhang, Z., Chen, S., Zhu, X., Wang, M.-Y., Yang, X., Ding, C., Han, J., Li, Q., & Duan, Y. (2023) · Acta Pharmacologica Sinica · doi:10.1038/s41401-023-01121-7 · Cited by 9

A2AR antagonists triggered the AMPK/m-TOR autophagic pathway to reverse the calcium-dependent cell damage in 6-OHDA induced model of PD

Sophronea, T., Agrawal, S., Kumari, N., Mishra, J., Walecha, V., & Luthra, P. M. (2024) · Neurochemistry International · doi:10.1016/j.neuint.2024.105793 · Cited by 9

Electroconvulsive seizures induce autophagy by activating the AMPK signaling pathway in the rat frontal cortex

Kim, S. H., Yu, H. S., Park, S., Park, H. G., Ahn, Y. M., Kang, U. G., & Kim, Y. S. (2019) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyz055 · Cited by 9

Vasorin Deletion in C57BL/6J Mice Induces Hepatocyte Autophagy through Glycogen-Mediated mTOR Regulation

Yang, L., Cheng, X., Shi, W., Li, H., Zhang, Q., Huang, S., Huang, X., Wen, S., Gan, J., Liao, Z., et al. (2022) · Nutrients · doi:10.3390/nu14173600 · Cited by 10

Metastasis in Neuroblastoma and Its Link to Autophagy

Jahangiri, L. (2023) · Life · doi:10.3390/life13030818 · Cited by 9

The regulatory effect of acetylation of HMGN2 and H3K27 on pyocyanin‐induced autophagy in macrophages by affecting Ulk1 transcription

Du, Y., Guo, H., Guo, L., Miao, J., Ren, H., Liu, K., Ren, L., He, J., Wang, X., Chen, J., et al. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16788 · Cited by 9

Cyclosporine A as a Cardioprotective Agent During Donor Heart Retrieval, Storage, or Transportation: Benefits and Limitations

Gao, L., Hicks, M., Villanueva, J. E., Doyle, A., Chew, H. C., Qui, M. R., Jabbour, A., Dhital, K. K., & Macdonald, P. S. (2019) · Transplantation · doi:10.1097/tp.0000000000002629 · Cited by 9

Dendrobium officinale flowers flavonoids enriched extract protects against acute ethanol-induced gastric ulcers via AMPK/PI3K signaling pathways

Zhang, Z., Xie, H., Farag, M. A., Li, Z., Wu, Q., & Shao, P. (2024) · Food Science and Human Wellness · doi:10.26599/fshw.2023.9250048 · Cited by 10

SFRP4 promotes autophagy and blunts FSH responsiveness through inhibition of AKT signaling in ovarian granulosa cells

Bérubé, M., Abedini, A., Lapointe, É., Gusscott, S., Brind’Amour, J., Zamberlam, G., & Boerboom, D. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01736-1 · Cited by 8

Neuromuscular electrical stimulation alleviates stroke-related sarcopenia by promoting satellite cells myogenic differentiation via AMPK-ULK1-Autophagy axis

Xiang, X., Huang, L., Luo, W., Qin, L., Bian, M., Chen, W., Han, G., Wang, N., Mo, G., Zhang, C., et al. (2025) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2025.03.021 · Cited by 10

Elevated Phosphate Levels Trigger Autophagy-Mediated Cellular Apoptosis in H9c2 Cardiomyoblasts

Liu, Y., Lin, K., Tamilselvi, S., Chen, W.-K., Shen, C.-Y., Chen, R., Day, C. H., Wu, H., Viswanadha, V. P., & Huang, C. (2017) · Cardiorenal Medicine · doi:10.1159/000479010 · Cited by 8

Bromelain activates the AMP-activated protein kinase-autophagy pathway to alleviate hepatic lipid accumulation

Hu, P.-A., Hsu, M., Chen, S.-H., Chen, C., Kou, Y. R., Huang, J., & Lee, T. (2022) · Journal of Food and Drug Analysis · doi:10.38212/2224-6614.3416 · Cited by 10

Calcitonin gene-related peptide exerts inhibitory effects on autophagy in the heart of mice

Schavinski, A. Z., Machado, J., Morgan, H. J. N., Lautherbach, N. E. S., Paula-Gomes, S., Kettelhut, Í. D. C., & Navegantes, L. C. C. (2021) · Peptides · doi:10.1016/j.peptides.2021.170677 · Cited by 8

Inhibition of autophagy initiation: A novel strategy for oral squamous cell carcinomas

El-Aziz, Y. S. A., McKay, M. J., Molloy, M. P., McDowell, B., Moon, E. A., Sioson, L., Sheen, A., Chou, A. S. Y., Gill, A. J., Jansson, P. J., et al. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2023.119627 · Cited by 8

Autophagy

Hsu, C. (2019) · The Chinese Journal of Physiology · doi:10.4103/cjp.cjp_25_19 · Cited by 8

Reduced Retinal Pigment Epithelial Autophagy Due to Loss of Rab12 Prenylation in a Human iPSC-RPE Model of Choroideremia

Raeker, M. Ö., Perera, N. D., Karoukis, A. J., Chen, L., Feathers, K. L., Ali, R. R., Thompson, D. A., & Fahim, A. T. (2024) · Cells · doi:10.3390/cells13121068 · Cited by 7

Genetic Determinants of the Effects of Training on Muscle and Adipose Tissue Homeostasis in Obesity Associated with Lymphedema

Vettori, A., Paolacci, S., Maltese, P. E., Herbst, K. L., Cestari, M., Michelini, S., Michelini, S., Samaja, M., & Bertelli, M. (2020) · Lymphatic Research and Biology · doi:10.1089/lrb.2020.0057 · Cited by 8

The Protective Effect of Flavonoids in the Diet on Autophagy-Related Cardiac Impairment

L’Abbate, S., & Kusmic, C. (2024) · Nutrients · doi:10.3390/nu16142207 · Cited by 8

Transcriptomic Changes Associated with Loss of Cell Viability Induced by Oxysterol Treatment of a Retinal Photoreceptor-Derived Cell Line: An In Vitro Model of Smith–Lemli–Opitz Syndrome

Pfeffer, B. A., Xu, L., & Fliesler, S. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052339 · Cited by 7

BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients

Carrasco‐Rozas, A., Fernández‐Simón, E., Suárez‐Calvet, X., Piñol‐Jurado, P., Alonso‐Pérez, J., de Luna, N., Schoser, B. G. H., Meinke, P., Domínguez‐González, C., Hernández‐Laín, A., et al. (2022) · American Journal Of Pathology · doi:10.1016/j.ajpath.2022.05.003 · Cited by 7

ER Stress, UPR and Virus Infections in Plants

Zhang, L., & Wang, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-32919-2_7 · Cited by 7

Metabolic Changes in Cardiac Aging

Hao, Y., & Liu, W. (2023) · Reviews in Cardiovascular Medicine · doi:10.31083/j.rcm2403082 · Cited by 8

The novel ginseng Rh2 derivative 2-deoxy-Rh2, exhibits potent anticancer effect via the AMPK/mTOR/autophagy signaling pathway against breast cancer

Li, X., Yin, J., Song, Q., Yang, Q., Li, C., & Gao, H. (2025) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2025.111422 · Cited by 6

Dopamine Receptor D3 Induces Transient, mTORC1-Dependent Autophagy That Becomes Persistent, AMPK-Mediated, and Neuroprotective in Experimental Models of Huntington’s Disease

Luis-Ravelo, D., Fumagallo-Reading, F., Febles-Casquero, A., López-Fernández, J., Marcellino, D. J., & González‐Hernández, T. (2025) · Cells · doi:10.3390/cells14090652 · Cited by 6

MTOR signaling regulates the development of airway mucous cell metaplasia associated with severe asthma

Kudrna, K. M., Vilches, L. F., Eilers, E. M., Maurya, S. K., Brody, S. L., Horani, A., Bailey, K. L., Wyatt, T. A., & Dickinson, J. D. (2025) · JCI Insight · doi:10.1172/jci.insight.187904 · Cited by 8

Multiple Mechanisms of the Therapeutic Effect of Trehalose in Inhibition of Experimental Neurodegeneration

Pupyshev, A. B., Короленко, Т. А., & Tikhonova, M. A. (2023) · Neurochemical Journal · doi:10.1134/s1819712423040190 · Cited by 6

Overexpression of SLC40A1 inhibits the malignancy of hepatocellular carcinoma MHCC-97H cells by stimulation of autophagy

Peng, Y., Yang, J., Li, Z., Chen, S., Tang, X., & Zhou, J. (2022) · Biomedical Signal Processing and Control · doi:10.1016/j.bspc.2022.103554 · Cited by 6

Potential Diets to Improve Mitochondrial Activity in Amyotrophic Lateral Sclerosis

Yoshikawa, S., Taniguchi, K., Sawamura, H., Ikeda, Y., Tsuji, A., & Matsuda, S. (2022) · Diseases · doi:10.3390/diseases10040117 · Cited by 7

AMPK promotes lysosomal and mitochondrial biogenesis via folliculin:FNIP1

Freemantle, J. B., & Hardie, D. G. (2023) · Life Metabolism · doi:10.1093/lifemeta/load027 · Cited by 6

Inhibition of SIRT2 promotes death of human cytomegalovirus-infected peripheral blood monocytes via apoptosis and necroptosis

Cheung, J., Remiszewski, S., Chiang, L. W., Ahmad, E., Pal, M., Rahman, S. A., Nikolovska‐Coleska, Z., & Chan, G. C. T. (2023) · Antiviral Research · doi:10.1016/j.antiviral.2023.105698 · Cited by 6

Autophagy studies in Bombyx mori

Tian, L., & Li, S. (2015) · Invertebrate survival journal · Cited by 6

Polyunsaturated fatty acid deficiency affects sulfatides and other sulfated glycans in lysosomes through autophagy‐mediated degradation

Wang, Y., Nakajima, T., Diao, P., Yamada, Y., Nakamura, K., Nakayama, J., Tanaka, N., Aoyama, T., & Kamijo, Y. (2020) · The FASEB Journal · doi:10.1096/fj.202000030rr · Cited by 6

Targeting Mitochondria with Sweat: Improving Mitochondrial Function with Physical Activity

Beleza, J., Rizo‐Roca, D., Ascensão, A. A. M. R., & Magalhães, J. (2018) · Springer eBooks · doi:10.1007/978-3-319-73344-9_18 · Cited by 6

LRBA deficiency impairs autophagy and contributes to enhanced antigen presentation and T-cell dysregulation

Sindram, E., Deau, M., Ligeon, L., Sánchez‐Martín, P., Nestel, S., Jung, S., Ruf, S., Mishra, P., Proietti, M., Günther, S., et al. (2025) · EMBO Reports · doi:10.1038/s44319-025-00504-7 · Cited by 8

The Role of Non-Coding RNAs in Regulating Cachexia Muscle Atrophy

Chen, G., Zou, J., He, Q., Xia, S., Xiao, Q., Du, R., Zhou, S., Zhang, C., Wang, N., & Feng, Y. (2024) · Cells · doi:10.3390/cells13191620 · Cited by 5

Effects of caloric restriction on retinal aging and neurodegeneration

Adornetto, A., Morrone, L. A., Satriano, A., Laganà, M. L., Licastro, E., Nucci, C., Corasaniti, M. T., Tonin, P., Bagetta, G., & Russo, R. (2020) · Progress in brain research · doi:10.1016/bs.pbr.2020.07.005 · Cited by 6

Methods to Determine the Role of Autophagy Proteins in C. elegans Aging

Henis‐Korenblit, S., & Meléndez, A. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-8873-0_37 · Cited by 4

Anabolic signaling and response in sarcopenia as a model for microgravity induced muscle deconditioning: A systematic review

Rundfeldt, L. C., Gunga, H., & Steinach, M. (2019) · REACH · doi:10.1016/j.reach.2019.100025 · Cited by 5

Autophagy: clocking in for the night shift

Brooks, R. C., & Dang, C. V. (2019) · The EMBO Journal · doi:10.15252/embj.2019102434 · Cited by 5

6,6′-((Methylazanedyl)bis(methylene))bis(2,4-dimethylphenol) Induces Autophagic Associated Cell Death through mTOR-Mediated Autophagy in Lung Cancer

Sriratanasak, N., Wattanathana, W., & Pithi Chanvorachote, B. (2022) · Molecules · doi:10.3390/molecules27196230 · Cited by 5

Role of autophagy in cell survival and death: Mechanisms and therapeutic implications

Pallen, S., Tiwari, S., & Pandey, R. K. (2025) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2025.06.015 · Cited by 4

The Dual Role of Autophagy in the Pathogenesis of Arboviruses With a Focus on JEV and DENV

Wang, H., Wang, Y., Li, Y., Chen, X., Wang, X., Wang, X., & Yu, S. (2025) · Reviews in Medical Virology · doi:10.1002/rmv.70073 · Cited by 4

Cremastrae Pseudobulbus Pleiones Pseudobulbus (CPPP) Against Non-Small-Cell Lung Cancer: Elucidating Effective Ingredients and Mechanism of Action

Cao, Y., Hao, Z., Liu, M.-M., Xue, J., Wang, Y., Wang, Y., Li, J., Lu, Y., Wang, C., & Shi, J. (2024) · Pharmaceuticals · doi:10.3390/ph17111515 · Cited by 4

Identification of ferroptosis-related genes as diagnostic biomarkers and therapeutic targets in sorafenib-resistant HCC via machine learning and experimental validation

Zhang, J., Geng, W., Sun, H., Chen, J., Fan, Y., & Tan, K. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115557 · Cited by 4

Early Cardiac Ischemia–Reperfusion Injury: Interactions of Autophagy with Galectin-3 and Oxidative Stress

Al‐Salam, S., Hashmi, S., Jagadeesh, G. S., Sudhadevi, M., Awwad, A., & Nemmar, A. (2024) · Biomedicines · doi:10.3390/biomedicines12112474 · Cited by 4

Subacute Reperfusion in Ischemic Hearts: Study of Autophagy and its Possible Interconnection with Receptor-Interacting Protein Kinase 3

Horvath, C. G., Ravíngerová, T., Suleiman, M. S., & Adameová, A. (2022) · Reviews in Cardiovascular Medicine · doi:10.31083/j.rcm2306213 · Cited by 4

Flaviviruses and Autophagy

Jordan, T. X., & Randall, G. C. (2014) · Wiley eBooks · doi:10.1002/9781118677551.ch6 · Cited by 4

Growth factor-independent mTORC1 signaling promotes primary cilia length via suppression of autophagy

Shin, J., Tighanimine, K., Cormerais, Y., Rosenthal, D. M., Niroula, P., Lapp, S. C., Kalafut, K. C., Cissé, M. Y., Schrötter, S., & Manning, B. D. (2025) · iScience · doi:10.1016/j.isci.2025.114204 · Cited by 3

Dysregulated autophagy in endometriosis: molecular mechanisms, controversies, and clinical implications

Tellez-Quijorna, C., Juan-Lopez, A., Eritja, N., Llobet‐Navàs, D., & Devis, L. (2025) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-025-01494-w · Cited by 3

Unveiling the Complexities: Exploring Mechanisms of Anthracyclineinduced Cardiotoxicity

Tayal, R., Mannan, A., Singh, S., Dhiman, S., & Singh, T. G. (2024) · Current Cardiology Reviews · doi:10.2174/011573403x322928241021100631 · Cited by 3

Regulation of the autophagy initiating kinase ULK1 by nutrients: Roles of mTORC1 and AMPK

Kim, J., & Guan, K. (2011) · Cell Cycle · doi:10.4161/cc.10.9.15291 · Cited by 96

AMPK and mTOR coordinate the regulation of Ulk1 and mammalian autophagy initiation

Shang, L., & Wang, X. (2011) · Autophagy · doi:10.4161/auto.7.8.15860 · Cited by 206

AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1

Kim, J., Kundu, M., Viollet, B., & Guan, K.-L. (2011) · Nature Cell Biology · doi:10.1038/ncb2152 · Cited by 7,227

The serine/threonine kinase ULK1 is a target of multiple phosphorylation events

Bach, M., Larance, M., James, D. E., & Ramm, G. (2011) · Biochemical Journal · doi:10.1042/bj20101894 · Cited by 233

The Association of AMPK with ULK1 Regulates Autophagy

Lee, J. W., Park, S., Takahashi, Y., & Wang, H.-G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015394 · Cited by 482