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LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing.

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p62/SQSTM1 Binds Directly to Atg8/LC3 to Facilitate Degradation of Ubiquitinated Protein Aggregates by Autophagy

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Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation

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A novel role of the mitochondrial permeability transition pore in (−)-gossypol-induced mitochondrial dysfunction

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The role of autophagy in the midgut epithelium of Parachela (Tardigrada)

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Innovations in Geroscience to enhance mobility in older adults

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Mechanism of Mir-218-5P in Autophagy, Apoptosis and Oxidative Stress in Rheumatoid Arthritis Synovial Fibroblasts is Mediated by Klf9 and Jak/Stat3 Pathways

Chen, M., Li, M., Zhang, N., Sun, W., Wang, H., & Wei, W. (2021) · Journal of Investigative Medicine · doi:10.1136/jim-2020-001437 · Cited by 36

Autophagy in Tenebrio molitor Immunity: Conserved Antimicrobial Functions in Insect Defenses

Jo, Y. H., Lee, J. H., Patnaik, B. B., Keshavarz, M., Lee, Y. S., & Han, Y. S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.667664 · Cited by 38

Copper-induced Genotoxicity, Oxidative Stress, and Alteration in Transcriptional Level of Autophagy-associated Genes in Snakehead Fish Channa punctatus

Kumar, M., Singh, S., Dwivedi, S., Trivedi, A., Dubey, I., & Trivedi, S. P. (2022) · Biological Trace Element Research · doi:10.1007/s12011-022-03301-8 · Cited by 40

Mitochondrial-Mediated Apoptosis Pathway in Alveolar Epithelial Cells Exposed to the Metals in Combustion-Generated Particulate Matter

Visalli, G., Baluce, B., Bertuccio, M. P., Picerno, I., & Pietro, A. D. (2015) · Journal of Toxicology and Environmental Health · doi:10.1080/15287394.2015.1024081 · Cited by 36

The activation of autophagy protects neurons and astrocytes against bilirubin-induced cytotoxicity

Qaisiya, M., Mardešić, P., Pastore, B., Tiribelli, C., & Bellarosa, C. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.09.056 · Cited by 35

A bibliometric analysis of autophagy in lung diseases from 2012 to 2021

Lin, F., Chen, Y., Mo, W., Zhou, H., Xiao, Z., Hu, S., Shi, X., Liu, M., Wei, J., Zhu, W., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1092575 · Cited by 36

Coronarin D induces reactive oxygen species-mediated cell death in human nasopharyngeal cancer cells through inhibition of p38 MAPK and activation of JNK

Chen, J., Hsieh, M., Lin, C., Lin, C.-C., Hsi, Y., Lo, Y., Chuang, Y., Hsieh, M.-J., & Chen, M. (2017) · Oncotarget · doi:10.18632/oncotarget.22444 · Cited by 35

Hedychium coronarium extract arrests cell cycle progression, induces apoptosis, and impairs migration and invasion in HeLa cervical cancer cells

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Protective Effects of Melatonin Against Zearalenone Toxicity on Porcine Embryos in vitro

Xu, Y. Q., Zhang, K., Sun, M., Lan, M., Wan, X., Zhang, Y., & Sun, S. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00327 · Cited by 35

Tension induces intervertebral disc degeneration via endoplasmic reticulum stress-mediated autophagy

Chen, J., Lin, Z., Deng, K., Shao, B., & Yang, D. (2019) · Bioscience Reports · doi:10.1042/bsr20190578 · Cited by 35

Tanshinone IIA ameliorates oxaliplatin-induced neurotoxicity via mitochondrial protection and autophagy promotion.

Cheng, W., Xiang, W., Wang, S., & Xu, K. L. (2019) · PubMed Central · Cited by 35

Cilostazol alleviate nicotine induced cardiomyocytes hypertrophy through modulation of autophagy by CTSB/ROS/p38MAPK/JNK feedback loop

Wang, S., Ni, X., Hu, K., Meng, F.-L., Li, M., Ma, X., Meng, T., Wu, H., Ge, D., Zhao, J., et al. (2020) · International Journal of Biological Sciences · doi:10.7150/ijbs.43825 · Cited by 35

Ectopic expression of DJ-1/PfpI domain containing Erianthus arundinaceus Glyoxalase III (EaGly III) enhances drought tolerance in sugarcane

Mohanan, M. V., Anunanthini, P., Padmanabhan, T. S. S., Selvarajan, D., Jayanarayanan, A. N., Arun Kumar, R., Ramalingam, S., Karuppasamy, S. N., Subbiah, R., Ram, B., et al. (2020) · Plant Cell Reports · doi:10.1007/s00299-020-02585-1 · Cited by 35

Rapamycin Removes Damaged Mitochondria and Protects Human Trabecular Meshwork (TM-1) Cells from Chronic Oxidative Stress

He, J. N., Zhang, S. D., Qu, Y., Wang, H. L., Tham, C. C. Y., Pang, C. P., & Chu, W. K. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1559-5 · Cited by 35

The over-expression of ERbeta modifies estradiol effects on mitochondrial dynamics in breast cancer cell line

Sastre-Serra, J., Nadal-Serrano, M., Pons, D. G., Roca, P., & Oliver, J. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.04.007 · Cited by 34

Thymol as a Potential Neuroprotective Agent: Mechanisms, Efficacy, and Future Prospects

Peng, X., Zhang, X., Sharma, G., & Dai, C. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c06461 · Cited by 36

Pathways for salvage and protection of the heart under stress: novel routes for cardiac rejuvenation

Cannata, A. N., Camparini, L., Sinagra, G., Giacca, M., & Loffredo, F. S. (2016) · Cardiovascular Research · doi:10.1093/cvr/cvw106 · Cited by 34

Identification of dual mechanisms mediating 5-hydroxytryptamine receptor 1F-induced mitochondrial biogenesis

Gibbs, W. S., Garrett, S. M., Beeson, C. C., & Schnellmann, R. G. (2017) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00324.2017 · Cited by 33

Decreased ceramide underlies mitochondrial dysfunction in Charcot‐Marie‐Tooth 2F

Schwartz, N. U., Linzer, R. W., Truman, J., Гуревич, М. А., Hannun, Y. A., Senkal, C. E., & Obeid, L. M. (2017) · The FASEB Journal · doi:10.1096/fj.201701067r · Cited by 37

Discovery of the novel autophagy inhibitor aumitin that targets mitochondrial complex I

Robke, L., Futamura, Y., Konstantinidis, G., Wilke, J., Aono, H., Mahmoud, Z., Watanabe, N., Wu, Y., Osada, H., Laraia, L., et al. (2018) · Chemical Science · doi:10.1039/c7sc05040b · Cited by 34

Modern ideas about cell death

Deev, R. V., Bilyalov, A. I., & Жампеисов, Т. М. (2018) · Genes and Cells · doi:10.23868/201805001 · Cited by 34

In-depth phenotypic characterization of reticulocyte maturation using mass cytometry

Thomson-Luque, R., Wang, C. C. Q., Ntumngia, F. B., Xu, S., Szekeres, K., Conway, A., Adapa, S. R., Barnes, S. J., Adams, J. H., & Jiang, R. H. Y. (2018) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2018.06.004 · Cited by 35

Knockdown of Long Non-Coding RNA GAS5 Increases miR-23a by Targeting ATG3 Involved in Autophagy and Cell Viability

Li, L., Huang, C., He, Y., Sang, Z., Liu, G., & Dai, H. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000492300 · Cited by 36

Antioxidant effect of human placenta hydrolysate against oxidative stress on muscle atrophy

Bak, D., Na, J., Im, S. I., Oh, C. T., Kim, J. Y., Park, S., Han, H. J., Seok, J., Choi, S. Y., Ko, E. J., et al. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27034 · Cited by 35

Autophagy in pulmonary hypertension: Emerging roles and therapeutic implications

Zhang, C., Zhao, F., Xu, S., Liu, J., Xing, X., & Yang, J. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28531 · Cited by 35

Inhibition of autophagy by hydroxychloroquine enhances antioxidant nutrients and delays postharvest fruit senescence of Ziziphus jujuba

Deng, B., Guo, M., Liu, H., Tian, S., & Zhao, X. (2019) · Food Chemistry · doi:10.1016/j.foodchem.2019.05.189 · Cited by 34

Melatonin and regulation of autophagy: Mechanisms and therapeutic implications

Wu, J., Bai, Y., Wang, Y., & Ma, J. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105279 · Cited by 34

Novel PET Biomarkers to Disentangle Molecular Pathways across Age-Related Neurodegenerative Diseases

Wilson, H., Politis, M., Rabiner, E. A., & Middleton, L. T. (2020) · Cells · doi:10.3390/cells9122581 · Cited by 34

Hepatic autophagy and mitophagy status in dairy cows with subclinical and clinical ketosis

Shen, T., Xu, F., Fang, Z., Loor, J. J., Ouyang, H., Chen, M., Jin, B., Wang, X., Shi, Z., Zhu, Y., et al. (2021) · Journal of Dairy Science · doi:10.3168/jds.2020-19150 · Cited by 34

Nanocarrier mediated autophagy: An emerging trend for cancer therapy

Singh, A., Handa, M., Ruwali, M., Flora, S. J. S., Shukla, R., & Kesharwani, P. (2021) · Process Biochemistry · doi:10.1016/j.procbio.2021.07.011 · Cited by 34

Icariin Protects H9c2 Rat Cardiomyoblasts from Doxorubicin-Induced Cardiotoxicity: Role of Caveolin-1 Upregulation and Enhanced Autophagic Response

Scicchitano, M., Carresi, C., Nucera, S., Ruga, S., Maiuolo, J., Macrì, R., Scarano, F., Bosco, F., Mollace, R., Cardamone, A., et al. (2021) · Nutrients · doi:10.3390/nu13114070 · Cited by 34

Perfluorooctane Sulfonate Induces Autophagy-Dependent Apoptosis through Spinster 1-Mediated lysosomal-Mitochondrial Axis and Impaired Mitophagy

Yao, X., Sha, S., Wang, Y., Sun, X., Cao, J., Kang, J., Jiang, L., Chen, M., & Ma, Y. (2016) · Toxicological Sciences · doi:10.1093/toxsci/kfw118 · Cited by 33

Regulatory role of exercise-induced autophagy for sarcopenia

Liang, J., Zeng, Z., Zhang, Y., & Chen, N. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2019.110789 · Cited by 33

DL0410, a novel dual cholinesterase inhibitor, protects mouse brains against Aβ-induced neuronal damage via the Akt/JNK signaling pathway

Zhou, D., Zhou, W., Song, J.-K., Feng, Z., Yang, R., Wu, S., Wang, L., Liu, A., & Du, G. (2016) · Acta Pharmacologica Sinica · doi:10.1038/aps.2016.87 · Cited by 33

TM9SF4 is a novel factor promoting autophagic flux under amino acid starvation

Sun, L., Meng, Z., Zhu, Y., Lu, J., Li, Z., Zhao, Q., Huang, Y., Jiang, L., & Yao, X. (2017) · Cell Death and Differentiation · doi:10.1038/cdd.2017.166 · Cited by 34

Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy

Bernstein, A. M., Ritch, R. H., & Wolosin, J. M. (2018) · Journal of Glaucoma · doi:10.1097/ijg.0000000000000919 · Cited by 33

Mitochondrial DNA content and oxidation in bipolar disorder and its role across brain regions

Bodenstein, D. F., Kim, H. K., Brown, N. C., Navaid, B., Young, L. T., & Andreazza, A. C. (2019) · Schizophrenia · doi:10.1038/s41537-019-0089-5 · Cited by 33

Autophagy Deficiency Leads to Impaired Antioxidant Defense via p62-FOXO1/3 Axis

Zhao, L., Li, H., Wang, Y., Zheng, A., Cao, L., & Liu, J. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/2526314 · Cited by 34

Maternal organic selenium supplementation during gestation improves the antioxidant capacity and reduces the inflammation level in the intestine of offspring through the NF-κB and ERK/Beclin-1 pathways

Mou, D., Ding, D., Yang, M., Jiang, X., Zhao, L., Che, L., Fang, Z., Xu, S., Lin, Y., Zhuo, Y., et al. (2020) · Food & Function · doi:10.1039/d0fo02274h · Cited by 35

Preventing Developmental Origins of Cardiovascular Disease: Hydrogen Sulfide as a Potential Target?

Hsu, C., & Tain, Y. (2021) · Antioxidants · doi:10.3390/antiox10020247 · Cited by 34

How Cells Deal with the Fluctuating Environment: Autophagy Regulation under Stress in Yeast and Mammalian Systems

Lei, Y., Huang, Y. J., Wen, X., Yin, Z., Zhang, Z., & Klionsky, D. J. (2022) · Antioxidants · doi:10.3390/antiox11020304 · Cited by 36

A Novel Role of Proline Oxidase in HIV-1 Envelope Glycoprotein-induced Neuronal Autophagy

Pandhare, J., Dash, S., Jones, B., Villalta, F., & Dash, C. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.652776 · Cited by 33

Reactive oxygen species H2O2 and OH, but not O2− promote oridonin-induced phagocytosis of apoptotic cells by human histocytic lymphoma U937 cells

Zang, L., He, H., Xu, Q., Yu, Y., Zheng, N., Liu, W., Hayashi, T., Tashiro, S., Onodera, S., & Ikejima, T. (2013) · International Immunopharmacology · doi:10.1016/j.intimp.2013.01.004 · Cited by 33

Oxidative stress, a new hallmark in the pathophysiology of Lafora progressive myoclonus epilepsy

Mateo, C. R., Aguado, C., García‐Giménez, J. L., Knecht, E., Sanz, P., & Pallardó, F. V. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.01.034 · Cited by 33

Established Principles and Emerging Concepts on the Interplay between Mitochondrial Physiology andS-(De)nitrosylation: Implications in Cancer and Neurodegeneration

Giacomo, G. D., Rizza, S., Montagna, C., & Filomeni, G. (2012) · International Journal of Cell Biology · doi:10.1155/2012/361872 · Cited by 33

Managing Erectile Dysfunction in Heart Failure

Giagulli, V. A., Moghetti, P., Kaufman, J., Guastamacchia, E., Iacoviello, M., & Triggiani, V. (2013) · Endocrine Metabolic & Immune Disorders - Drug Targets · doi:10.2174/1871530311313010015 · Cited by 33

MKK3 influences mitophagy and is involved in cigarette smoke-induced inflammation

Mannam, P., Rauniyar, N., Lam, T. T., Luo, R., Lee, P. J., & Srivastava, A. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.10.001 · Cited by 33

Mycotoxin‐assisted mitochondrial dysfunction and cytotoxicity: Unexploited tools against proliferative disorders

Islam, M. T., Mishra, S. K., Tripathi, S., de Alencar, M. V. O. B., Sousa, J. M. D. C. E., Rolim, H. M. L., de Medeiros, M. D. G. F., Ferreira, P. M. P., Rouf, R., Uddin, S. J., et al. (2018) · IUBMB Life · doi:10.1002/iub.1932 · Cited by 33

Title efficacy of phosphodiesterase 5 inhibitor on distant burn-induced muscle autophagy, microcirculation, and survival rate

Hosokawa, S., Koseki, H., Nagashima, M., Maeyama, Y., Yomogida, K., Mehr, C. R., Rutledge, M., Greenfeld, H., Kaneki, M., Tompkins, R. G., et al. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00078.2013 · Cited by 32

The Roles of Mitochondria in Autophagic Cell Death

Chen, Z., Liu, X., & Ma, S. (2016) · Cancer Biotherapy and Radiopharmaceuticals · doi:10.1089/cbr.2016.2057 · Cited by 32

17β-estradiol ameliorates oxidative stress and blue light-emitting diode-induced retinal degeneration by decreasing apoptosis and enhancing autophagy

Wei, Q., Liang, X., Ye, P., Yu, D., Zhang, R., Jin, H., Fan, J., Cai, W., Ren, C., & Yu, J. (2018) · Drug Design Development and Therapy · doi:10.2147/dddt.s176349 · Cited by 32

Familiness, socio-emotional goals and the internationalization of French family SMEs

Basly, S., & Saunier, P.-L. (2019) · Journal of International Entrepreneurship · doi:10.1007/s10843-019-00265-0 · Cited by 32

Distinctive Evidence Involved in the Role of Endocannabinoid Signalling in Parkinson’s Disease: A Perspective on Associated Therapeutic Interventions

Behl, T., Kaur, G., BUNGAU, S. G., Jhanji, R., Kumar, A., Mehta, V., Zengin, G., Brata, R. D., Hassan, S. S. U., & Frățilă, O. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176235 · Cited by 34

Selenium triggers Nrf2-AMPK crosstalk to alleviate cadmium-induced autophagy in rabbit cerebrum

Xue, H., Cao, H., Xing, C., Feng, J., Zhang, L., Zhang, C., Hu, G., & Yang, F. (2021) · Toxicology · doi:10.1016/j.tox.2021.152855 · Cited by 32

Small Molecules Targeting Programmed Cell Death in Breast Cancer Cells

Maniam, S., & Maniam, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22189722 · Cited by 33

Mitophagy in Ischaemia/Reperfusion Induced Cerebral Injury

Liu, K., Sun, Y., Gu, Z., Shi, N., Zhang, T., & Sun, X. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1033-0 · Cited by 32

Effect of the pituitary adenylate cyclase-activating polypeptide on the autophagic activation observed in in vitro and in vivo models of Parkinson's disease

Lamine-Ajili, A., Fahmy, A. M., Létourneau, M., Chatenet, D., Labonté, P., Vaudry, D., & Fournier, A. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.01.005 · Cited by 32

Nature and Implications of Oxidative and Nitrosative Stresses in Autoimmune Hepatitis

Czaja, A. J. (2016) · Digestive Diseases and Sciences · doi:10.1007/s10620-016-4247-6 · Cited by 32

Maternal L-Carnitine Supplementation Improves Brain Health in Offspring from Cigarette Smoke Exposed Mothers

Chan, Y. L., Saad, S., Al‐Odat, I., Oliver, B. G. G., Pollock, C. A., Jones, N. M., & Chen, H. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00033 · Cited by 33

Characterizing Adversity of Lysosomal Accumulation in Nonclinical Toxicity Studies: Results from the 5th ESTP International Expert Workshop

Lenz, B. F., Braendli-Baiocco, A., Engelhardt, J. A., Fant, P., Fischer, H., Francke, S., Fukuda, R., Gröters, S., Harada, T., Harleman, H., et al. (2018) · Toxicologic Pathology · doi:10.1177/0192623317749452 · Cited by 32

Targeting mitochondria in dermatological therapy: beyond oxidative damage and skin aging

Wikramanayake, T. C., Chéret, J., Sevilla, A., Birch‐Machin, M. A., & Paus, R. (2022) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2022.2049756 · Cited by 31

Development of a Golgi-targeted superoxide anion fluorescent probe for elucidating protein GOLPH3 function in myocardial ischemia-reperfusion injury

Li, A., Liu, Y., Labapuchi, Chen, Z., Li, S., Zhong, R., Cheng, D., He, L., & He, L. (2023) · Analytica Chimica Acta · doi:10.1016/j.aca.2023.341100 · Cited by 31

Salidroside protects retinal endothelial cells against hydrogen peroxide-induced injury via modulating oxidative status and apoptosis

Shi, K., Wang, X., Zhu, J., Cao, G., Zhang, K., & Su, Z. (2015) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2015.1038212 · Cited by 31

Novel and emerging targeted-based cancer therapy agents and methods

Hojjat‐Farsangi, M. (2015) · Tumor Biology · doi:10.1007/s13277-015-3184-x · Cited by 31

Stress is an agonist for the induction of programmed cell death: A review

Zhou, D. R., Eid, R., Boucher, É. L., Miller, K. A., Mandato, C. A., & Greenwood, M. T. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.12.001 · Cited by 32

An evolutionary, or “Mitocentric” perspective on cellular function and disease

Brown, J. A., Sammy, M. J., & Ballinger, S. W. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101568 · Cited by 31

Pregnancy as a model for aging

Giller, A., Andrawus, M., Gutman, D., & Atzmon, G. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101093 · Cited by 33

Free Radical Medicine and Biology

Das, K. K., Das, S. N., Biradar, M. S., Bobbarala, V., & Tata, S. S. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.77829 · Cited by 32

Integrating DNA damage response and autophagy signalling axis in ultraviolet-B induced skin photo-damage: a positive association in protecting cells against genotoxic stress

Umar, S. A., & Tasduq, S. A. (2020) · RSC Advances · doi:10.1039/d0ra05819j · Cited by 33

Halogen-Induced Chemical Injury to the Mammalian Cardiopulmonary Systems

Addis, D. R., Aggarwal, S., Lazrak, A., Jilling, T., & Matalon, S. (2021) · Physiology · doi:10.1152/physiol.00004.2021 · Cited by 29

Autophagy modulation in multiple sclerosis and experimental autoimmune encephalomyelitis

Shen, D., Liu, K., Wang, H., & Wang, H. (2022) · Clinical & Experimental Immunology · doi:10.1093/cei/uxac017 · Cited by 32

From clinical description, to in vitro and animal studies, and backward to patients: Oxidative stress and mitochondrial dysfunction in Fanconi anemia

Pagano, G., Talamanca, A. A., Castello, G., d’Ischia, M., Pallardó, F. V., Petrović, S. Ž., Porto, B., Tiano, L., & Zatterale, A. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.01.015 · Cited by 30

Insulin receptor substrate-1 prevents autophagy-dependent cell death caused by oxidative stress in mouse NIH/3T3 cells

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The phenoptosis problem: What is causing the death of an organism? Lessons from acute kidney injury

Zorov, D. B., Plotnikov, E. Y., Jankauskas, S. S., Исаев, Н. К., Silachev, D. N., Zorova, L. D., Pevzner, I. B., Pulkova, N. V., Zorov, S. D., & Morosanova, M. A. (2012) · Biochemistry (Moscow) · doi:10.1134/s0006297912070073 · Cited by 31

In-Depth Proteomics Identifies a Role for Autophagy in Controlling Reactive Oxygen Species Mediated Endothelial Permeability

Patella, F., Neilson, L. J., Athineos, D., Erami, Z., Anderson, K. I., Blyth, K., Ryan, K. M., & Zanivan, S. R. (2016) · Journal of Proteome Research · doi:10.1021/acs.jproteome.6b00166 · Cited by 32

The effects of resveratrol on aging vessels

Diaz, M., Degens, H., Vanhees, L., Austin, C., & Azzawi, M. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.09.016 · Cited by 31

Ultraviolet B radiation down-regulates ULK1 and ATG7 expression and impairs the autophagy response in human keratinocytes

Chen, X., Li, L., Xu, S., Bu, W., Chen, K., Li, M., & Gu, H. (2017) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2017.08.043 · Cited by 31

Oxidative stress-induced autophagy: Role in pulmonary toxicity

Malaviya, R., Laskin, J. D., & Laskin, D. L. (2014) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2013.12.022 · Cited by 30

Beyond multiple mechanisms and a unique drug: Defective autophagy as pivotal player in cerebral cavernous malformation pathogenesis and implications for targeted therapies

Marchi, S., Trapani, E., Corricelli, M., Goitre, L., Pinton, P., & Retta, S. F. (2016) · Rare Diseases · doi:10.1080/21675511.2016.1142640 · Cited by 32

A research update on the anticancer effects of bufalin and its derivatives (Review)

Lan, Y., Lou, J., Jiang, X., Wang, X., Xing, J., Li, S., & Zhang, B. (2019) · Oncology Letters · doi:10.3892/ol.2019.10062 · Cited by 30

The Potential Role of Nrf2 Signaling in Leishmania Infection Outcomes

Vivarini, Á. D. C., & Lopes, U. G. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00453 · Cited by 30

Comparing Early Eukaryotic Integration of Mitochondria and Chloroplasts in the Light of Internal ROS Challenges: Timing is of the Essence

Speijer, D., Hammond, M., & Lukeš, J. (2020) · mBio · doi:10.1128/mbio.00955-20 · Cited by 31

Oregano Phytocomplex Induces Programmed Cell Death in Melanoma Lines via Mitochondria and DNA Damage

Nanni, V., Marco, G. D., Sacchetti, G., Canini, A., & Gismondi, A. (2020) · Foods · doi:10.3390/foods9101486 · Cited by 33

Synthesis of Indofulvin Pseudo‐Natural Products Yields a New Autophagy Inhibitor Chemotype

Burhop, A., Bag, S., Grigalunas, M., Woitalla, S., Bodenbinder, P., Brieger, L., Carsten Strohmann, B., Pahl, A., Sievers, S., & Waldmann, H. (2021) · Advanced Science · doi:10.1002/advs.202102042 · Cited by 30

Melatonin Induces Autophagy via Reactive Oxygen Species-Mediated Endoplasmic Reticulum Stress Pathway in Colorectal Cancer Cells

Chok, K. C., Koh, R. Y., Ng, M. G., Ng, P. Y., & Chye, S. M. (2021) · Molecules · doi:10.3390/molecules26165038 · Cited by 37

Nogo-A reduces ceramide de novo biosynthesis to protect from heart failure

Sasset, L., Manzo, O. L., Zhang, Y., Marino, A., Rubinelli, L., Riemma, M. A., Chalasani, M. L. S., Dasoveanu, D., Roviezzo, F., Jankauskas, S. S., et al. (2022) · Cardiovascular Research · doi:10.1093/cvr/cvac108 · Cited by 31

Nootkatone Supplementation Ameliorates Carbon Tetrachloride-Induced Acute Liver Injury via the Inhibition of Oxidative Stress, NF-κB Pathways, and the Activation of Nrf2/HO-1 Pathway

Dai, C., Zhang, X., Lin, J., & Shen, J. (2023) · Antioxidants · doi:10.3390/antiox12010194 · Cited by 30

Dimethyl fumarate ameliorates parkinsonian pathology by modulating autophagy and apoptosis via Nrf2-TIGAR-LAMP2/Cathepsin D axis

Khot, M., Sood, A., Tryphena, K. P., Pinjala, P., Srivastava, S., Singh, S. B., & Khatri, D. K. (2023) · Brain Research · doi:10.1016/j.brainres.2023.148462 · Cited by 30

Autophagy activation aggravates neuronal injury in the hippocampus of vascular dementia rats

Liu, B., Tang, J. Y., Zhang, J., Li, S., Yuan, M., & Wang, R. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.137576 · Cited by 30

Pomegranate and green tea extracts protect against ER stress induced by a high-fat diet in skeletal muscle of mice

Rodriguez, J., Gilson, H., Jamart, C., Naslain, D., Pierre, N., Deldicque, L., & Francaux, M. (2014) · European Journal of Nutrition · doi:10.1007/s00394-014-0717-9 · Cited by 30

Do antioxidants inhibit oxidative‐stress‐induced autophagy of tenofibroblasts?

Kim, R.-J., Hah, Y., Sung, C., Kang, J., & Park, H. B. (2014) · Journal of Orthopaedic Research® · doi:10.1002/jor.22608 · Cited by 30

Ketogenic diet change cPLA2/clusterin and autophagy related gene expression and correlate with cognitive deficits and hippocampal MFs sprouting following neonatal seizures

Ni, H., Zhao, D., & Tian, T. (2015) · Epilepsy Research · doi:10.1016/j.eplepsyres.2015.11.021 · Cited by 30

Sickness-Associated Anorexia: Mother Nature’s Idea of Immunonutrition?

van Niekerk, G., Isaacs, A. W., Nell, T. A., & Engelbrecht, A. (2016) · Mediators of Inflammation · doi:10.1155/2016/8071539 · Cited by 32

Pyrrolidine Dithiocarbamate (PDTC) Inhibits DON-Induced Mitochondrial Dysfunction and Apoptosis via the NF-κB/iNOS Pathway

Wan, D., Wu, Q.-H., Qu, W., Liu, G., & Wang, X. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/1324173 · Cited by 31

Augmenter of Liver Regeneration Protects against Ethanol-Induced Acute Liver Injury by Promoting Autophagy

Liu, L., Xie, P., Li, W., Wu, Y., & An, W. (2018) · American Journal Of Pathology · doi:10.1016/j.ajpath.2018.11.006 · Cited by 29

Disruption of peroxisome proliferator–activated receptor γ coactivator (PGC)-1α reverts key features of the neoplastic phenotype of glioma cells

Bruns, I., Sauer, B., Burger, M. C., Eriksson, J. A., Hofmann, U., Braun, Y., Harter, P. N., Luger, A., Ronellenfitsch, M. W., Steinbach, J. P., et al. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006993 · Cited by 31

Pathophysiological characterization of MERRF patient-specific induced neurons generated by direct reprogramming

Paz, M. V., Povea-Cabello, S., Villalón-García, I., Suarez-Rivero, J. M., Álvarez-Córdoba, M., de la Mata, M., Talaverón-Rey, M., Jackson, S., & Sánchez-Alcázar, J. A. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2019.02.010 · Cited by 31

REVIEW ARTICLE Autophagy, mitochondria and oxidative stress: cross-talk and redox

Lee, J., Giordano, S. S., & Zhang, J. (2013)

Roles of Autophagy in Oxidative Stress

Yun, H. R., Jo, Y. H., Kim, J., Shin, Y., Kim, S. S., & Choi, T. G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093289 · Cited by 413

The Roles of Autophagy in Oxidative Stress.

Mehrdar, M. T., & Rasool, M. (2025) · PubMed · doi:10.32598/ari.80.6.3391

Redox homeostasis, oxidative stress and mitophagy

Garza-Lombó, C., Pappa, A., Panayiotidis, M. I., & Franco, R. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.01.002 · Cited by 168

Oxidative Stress, Redox Signaling, and Autophagy: Cell Death Versus Survival

Navarro-Yepes, J., Burns, M., Anandhan, A., Khalimonchuk, O., Razo, L. M. D., Quintanilla‐Vega, B., Pappa, A., Panayiotidis, M. I., & Franco, R. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5837 · Cited by 467