The role of the Atg1/ULK1 complex in autophagy regulation

TOR signaling in growth and metabolism

Wullschleger, S., Loewith, R., & Hall, M. N. (2006) · Cell · doi:10.1016/j.cell.2006.01.016 · Cited by 5,787

p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

Bjørkøy, G., Lamark, T., Brech, A., Outzen, H., Perander, M., Øvervatn, A., Stenmark, H., & Johansen, T. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200507002 · Cited by 3,276

Defining the role of mTOR in cancer

Guertin, D. A., & Sabatini, D. M. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.05.008 · Cited by 2,833

Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

Ravikumar, B., Vacher, C., Berger, Z., Davies, J. E., Luo, S., Oroz, L. G., Scaravilli, F., Easton, D. F., Duden, R., O'Kane, C. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1362 · Cited by 2,347

Autophagosome formation: core machinery and adaptations

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

Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice.

Komatsu, M., Waguri, S., Koike, M., Sou, Y.-S., Ueno, T., Hara, T., Mizushima, N., Iwata, J.-I., Ezaki, J., Murata, S., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.035 · Cited by 2,124

Nutrient-dependent mTORC1 Association with the ULK1–Atg13–FIP200 Complex Required for Autophagy

Hosokawa, N., Hara, T., Kaizuka, T., Kishi, C., Takamura, A., Miura, Y., Iemura, S.-I., Natsume, T., Takehana, K., Yamada, N., et al. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-12-1248 · Cited by 2,076

ULK-Atg13-FIP200 Complexes Mediate mTOR Signaling to the Autophagy Machinery

Jung, C. H., Jun, C. B., Ro, S.-H., Kim, Y.-M., Otto, N. M., Cao, J., Kundu, M., & Kim, D.-H. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-12-1249 · Cited by 2,025

Autophagy: molecular machinery for self-eating

Yorimitsu, T., & Klionsky, D. J. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401765 · Cited by 1,566

ULK1·ATG13·FIP200 Complex Mediates mTOR Signaling and Is Essential for Autophagy

Ganley, I. G., Lam, D. H., Wang, J., Ding, X., Chen, S., & Jiang, X. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m900573200 · Cited by 1,447

Molecular mechanisms of selective autophagy in Drosophila

Gohel, R., Kournoutis, A., Petridi, S., & Nezis, I. P. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2019.08.003 · Cited by 27

Nutrient Sensor mTORC1 Regulates Insulin Secretion by Modulating β-Cell Autophagy

Israeli, T., Riahi, Y., Garzon, P., Louzada, R. A. N., Werneck‐de‐Castro, J. P., Blandino-Rosano, M., Yeroslaviz-Stolper, R., Kadosh, L., Tornovsky-Babeay, S., Hacker, G., et al. (2021) · Diabetes · doi:10.2337/db21-0281 · Cited by 28

Autophagy in the Neuronal Ceroid Lipofuscinoses (Batten Disease)

Kim, W. D., Wilson‐Smillie, M. L. D. M., Thanabalasingam, A., Lefrançois, S., Cotman, S. L., & Huber, R. J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.812728 · Cited by 29

Fission Yeast Autophagy Machinery

Xu, D., & Du, L. (2022) · Cells · doi:10.3390/cells11071086 · Cited by 29

Regulation of autophagy by Forkhead box (FOX) O transcription factors

van der Vos, K. E., Gomez‐Puerto, M. C., & Coffer, P. J. (2011) · Advances in Biological Regulation · doi:10.1016/j.advenzreg.2011.10.002 · Cited by 29

Autophagy Suppression by Appendicitis and Appendectomy Protects Against Colitis

Cheluvappa, R., Luo, A. S., & Grimm, M. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000034 · Cited by 27

Constitutive Activation of PINK1 Protein Leads to Proteasome-mediated and Non-apoptotic Cell Death Independently of Mitochondrial Autophagy

Akabane, S., Matsuzaki, K., Yamashita, S., Arai, K., Okatsu, K., Kanki, T., Matsuda, N., & Oka, T. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.714923 · Cited by 27

In Silico Knockout Studies of Xenophagic Capturing of Salmonella

Scheidel, J., Amstein, L., Ackermann, J., Đikić, I., & Koch, I. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005200 · Cited by 26

Dysregulation of autophagy during photoaging reduce oxidative stress and inflammatory damage caused by UV

Zhang, Z., Tan, R., Xiong, Z., Feng, Y., & Chen, L. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1562845 · Cited by 31

Autophagy and PTEN in DNA damage-induced senescence

Sharma, A., & Almasan, A. (2021) · Advances in cancer research · doi:10.1016/bs.acr.2021.01.006 · Cited by 26

Cardiomyocyte Atrophy, an Underestimated Contributor in Doxorubicin-Induced Cardiotoxicity

Chen, D.-S., Yan, J., & Yang, P. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.812578 · Cited by 26

β Cell and Autophagy: What Do We Know?

Mohammadi‐Motlagh, H., Sadeghalvad, M., Yavari, N., Primavera, R., Soltani, S., Chetty, S. S., Ganguly, A., Regmi, S., Fløyel, T., Kaur, S., et al. (2023) · Biomolecules · doi:10.3390/biom13040649 · Cited by 27

The “Janus-Faced Role” of Autophagy in Neuronal Sickness: Focus on Neurodegeneration

Viscomi, M. T., & D’Amelio, M. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8296-3 · Cited by 26

Autophagy suppresses cell migration by degrading GEF-H1, a RhoA GEF

Yoshida, T., Tsujioka, M., Honda, S., Tanaka, M., & Shimizu, S. (2016) · Oncotarget · doi:10.18632/oncotarget.8883 · Cited by 26

Differences in the starvation-induced autophagy response in MDA-MB-231 and MCF-7 breast cancer cells

Zhu, W., Qu, H., Xu, K., Jia, B., Li, H., Yi-min, D., Liu, G., Wei, H., & Zhao, H. (2017) · Animal Cells and Systems · doi:10.1080/19768354.2017.1330763 · Cited by 26

The STING controlled cytosolic-DNA activated innate immune pathway and microbial disease

Konno, H., & Barber, G. N. (2014) · Microbes and Infection · doi:10.1016/j.micinf.2014.10.002 · Cited by 26

Astragaloside IV alleviates senescence of vascular smooth muscle cells through activating Parkin-mediated mitophagy

Li, H., Xu, J., Zhang, Y., Hong, L., He, Z., Zeng, Z., & Zhang, L. (2022) · Human Cell · doi:10.1007/s13577-022-00758-6 · Cited by 25

The identification and analysis of phosphorylation sites on the Atg1 protein kinase

Yeh, Y.-Y., Shah, K. H., Chou, C., Hsiao, H., Wrasman, K., Stephan, J. S., Stamatakos, D., Khoo, K., & Herman, P. K. (2011) · Autophagy · doi:10.4161/auto.7.7.15155 · Cited by 26

Involvement of autophagy in tri-ortho-cresyl phosphate- induced delayed neuropathy in hens

Song, F., Kou, R., Zou, C., Gao, Y., Zeng, T., & Xie, K. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.10.017 · Cited by 25

Signaling in the Physiology and Pathophysiology of Pancreatic Stellate Cells – a Brief Review of Recent Advances

Kusiak, A. A., Szopa, M. D., Jakubowska, M. J., & Ferdek, P. E. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00078 · Cited by 28

Protein Homeostasis Networks and the Use of Yeast to Guide Interventions in Alzheimer’s Disease

Dhakal, S., & Macreadie, I. G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218014 · Cited by 26

Melatonin Modulates Neuronal Cell Death Induced by Endoplasmic Reticulum Stress under Insulin Resistance Condition

Song, J., & Kim, O. Y. (2017) · Nutrients · doi:10.3390/nu9060593 · Cited by 23

Propofol-induced MiR-20b expression initiates endogenous cellular signal changes mitigating hypoxia/re-oxygenation-induced endothelial autophagy in vitro

Lu, Y., Wang, S., Cai, S., Gu, X., Wang, J., Yang, Y., Hu, Z., Zhang, X.-H., Ye, Y., Shen, S., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02828-9 · Cited by 25

Autophagy and antiviral defense

Ke, P. (2021) · IUBMB Life · doi:10.1002/iub.2582 · Cited by 23

Research progress on the relationship between autophagy and chronic complications of diabetes

Ge, X., Wang, L., Fei, A., Ye, S., & Zhang, Q. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.956344 · Cited by 25

Decreased Whole‐Body Fat Mass Produced by Chronic Alcohol Consumption is Associated with Activation of S6K1‐Mediated Protein Synthesis and Increased Autophagy in Epididymal White Adipose Tissue

Crowell, K. T., Steiner, J. L., Coleman, C. S., & Lang, C. H. (2016) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13159 · Cited by 24

Angelicin inhibits the malignant behaviours of human cervical cancer potentially via inhibiting autophagy

Wang, Y., Chen, Y., Chen, X., Liang, Y., Yang, D., Dong, J., Yang, N., & Liang, Z. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.7985 · Cited by 24

Novel strategies to overcome chemoresistance in human glioblastoma

Tang, Q., Ren, T., Bai, P., Wang, X., Zhao, L., Zhong, R., & Sun, G. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116588 · Cited by 24

Transiently expressed ATG16L1 inhibits autophagosome biogenesis and aberrantly targets RAB11-positive recycling endosomes

Li, J., Chen, Z., Stang, M. T., & Gao, W. (2016) · Autophagy · doi:10.1080/15548627.2016.1256521 · Cited by 23

Roles of Autophagy in Ischemic Heart Diseases and the Modulatory Effects of Chinese Herbal Medicine

Wang, D., Weiqing, Y., Liu, Y., Zhong, G., Zhao, Z., Xia, Y., & Liu, Q. (2017) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x17500768 · Cited by 23

Noninvasive diagnostic criteria for nonalcoholic steatohepatitis based on gene expression levels in peripheral blood mononuclear cells

Kado, A., Tsutsumi, T., Enooku, K., Fujinaga, H., Ikeuchi, K., Okushin, K., Moriya, K., Yotsuyanagi, H., & Koike, K. (2019) · Journal of Gastroenterology · doi:10.1007/s00535-019-01565-x · Cited by 23

Autophagy Regulates Craniofacial Bone Acquisition

Thomas, N., Choi, H. K., Wei, X., Wang, L., Mishina, Y. M., Guan, J., & Liu, F. (2019) · Calcified Tissue International · doi:10.1007/s00223-019-00593-2 · Cited by 23

Docosahexaenoic acid promotes the formation of autophagosomes in MCF-7 breast cancer cells through oxidative stress-induced growth inhibitor 1 mediated activation of AMPK/mTOR pathway

Tsai, C.-H., Lii, C., Wang, T., Liu, K., Chen, H., Huang, C., & Li, C. (2021) · Food and Chemical Toxicology · doi:10.1016/j.fct.2021.112318 · Cited by 28

HDAC6 Inhibition Extinguishes Autophagy in Cancer: Recent Insights

Passaro, E., Papulino, C., Chianese, U., Toraldo, A., Congi, R., Gaudio, N. D., Nicoletti, M. M., Benedetti, R., & Altucci, L. (2021) · Cancers · doi:10.3390/cancers13246280 · Cited by 25

Recent Advances in Chinese Herbal Medicine for Cerebral Ischemic Reperfusion Injury

Huang, P. C., Wan, H., Shao, C., Li, C., Zhang, L., & He, Y. T. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.688596 · Cited by 23

Therapeutic potential of targeting mTOR in T-cell acute lymphoblastic leukemia (Review)

Evangelisti, C., Evangelisti, C., Chiarini, F., Lonetti, A., Buontempo, F., Bressanin, D., Cappellini, A., Orsini, E., McCubrey, J. A., & Martelli, A. M. (2014) · International Journal of Oncology · doi:10.3892/ijo.2014.2525 · Cited by 26

Goniothalamin induces apoptosis associated with autophagy activation through MAPK signaling in SK-BR-3 cells

Innajak, S., Mahabusrakum, W., & Watanapokasin, R. Y. (2016) · Oncology Reports · doi:10.3892/or.2016.4655 · Cited by 22

Caspase-1 participates in apoptosis of salivary glands in Rhipicephalus haemaphysaloides

Yu, X., Zhou, Y., Cao, J., Zhang, H., Gong, H., & Zhou, J. (2017) · Parasites & Vectors · doi:10.1186/s13071-017-2161-1 · Cited by 23

The intracellular microbial sensor NLRP4 directs Rho-actin signaling to facilitate Group A Streptococcus-containing autophagosome-like vacuole formation

Nozawa, T., Aikawa, C., Minowa‐Nozawa, A., & Nakagawa, I. (2017) · Autophagy · doi:10.1080/15548627.2017.1358343 · Cited by 23

Yorkie Growth-Promoting Activity Is Limited by Atg1-Mediated Phosphorylation

Tyra, L. K., Nandi, N., Tracy, C., & Krämer, H. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.01.011 · Cited by 26

Roles of circRNAs on tumor autophagy

Cui, W., Dang, Q., Chen, C., Yuan, W., & Sun, Z. (2021) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2021.01.002 · Cited by 23

Is autophagy induction by PARP inhibitors a target for therapeutic benefit?

Elshazly, A. M., NGUYEN, T. V. V., & Gewirtz, D. A. (2022) · Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics · doi:10.32604/or.2022.026459 · Cited by 22

Acetylation modification in the regulation of macroautophagy

Huang, L., & Guo, H. (2024) · Advanced Biotechnology · doi:10.1007/s44307-024-00027-7 · Cited by 24

Dissecting the function of Atg1 complex in Dictyostelium autophagy reveals a connection with the pentose phosphate pathway enzyme transketolase

Mesquita, A., Tábara, L. C., Martínez-Costa, Ó. H., Santos-Rodrigo, N., Vincent, O., & Escalante, R. (2015) · Open Biology · doi:10.1098/rsob.150088 · Cited by 22

Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications

Chen, H., Liu, C.-C., & Chen, R. (2016) · Cell Division · doi:10.1186/s13008-016-0017-2 · Cited by 21

Autophagy – molecular mechanism, apoptosis and cancer

Polewska, J. (2012) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/17322693.1021109 · Cited by 22

Oncosuppressive functions of tribbles pseudokinase 3

Salazar‐Roa, M., Lorente, M., Orea‐Soufi, A., Dávila, D., Erazo, T., Lizcano, J. M., Carracedo, A., Kiss‐Toth, E., & Velasco, G. (2015) · Biochemical Society Transactions · doi:10.1042/bst20150124 · Cited by 24

Structural insights into pro-aggregation effects of C. elegans CRAM-1 and its human ortholog SERF2

Balasubramaniam, M., Ayyadevara, S., & Reis, R. J. S. (2018) · Scientific Reports · doi:10.1038/s41598-018-33143-1 · Cited by 24

P38α MAPK coordinates the activities of several metabolic pathways that together induce atrophy of denervated muscles

Odeh, M., Tamir, Y., Haas, T., & Bengal, E. (2019) · FEBS Journal · doi:10.1111/febs.15070 · Cited by 22

Cancer Cachexia Induces Preferential Skeletal Muscle Myosin Loss When Combined With Denervation

Yamada, T., Ashida, Y., Tatebayashi, D., Abe, M., & Himori, K. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00445 · Cited by 22

Blockade of HCN2 Channels Provides Neuroprotection Against Ischemic Injury via Accelerating Autophagic Degradation in Hippocampal Neurons

Chen, C., Liu, L., Shu, Y.-Q., Jing, P., Lu, Y., Zhang, X., Zong, X., Guo, L., & Li, C.-J. (2020) · Neuroscience Bulletin · doi:10.1007/s12264-020-00513-7 · Cited by 22

Autophagy coordinates chondrocyte development and early joint formation in zebrafish

Moss, J. J., Wirth, M., Tooze, S. A., Lane, J. D., & Hammond, C. L. (2021) · The FASEB Journal · doi:10.1096/fj.202101167r · Cited by 22

The emerging roles of ATG1/ATG13 kinase complex in plants

Wang, Q., & Hou, S. (2022) · Journal of Plant Physiology · doi:10.1016/j.jplph.2022.153653 · Cited by 21

Regulation of transferrin receptor trafficking by optineurin and its disease-associated mutants

Moharir, S. C., Sirohi, K., & Swarup, G. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.06.019 · Cited by 22

Loss of miR-144/451 alleviates β-thalassemia by stimulating ULK1-mediated autophagy of free α-globin

Keith, J., Christakopoulos, G. E., Fernandez, A. G., Yao, Y., Zhang, J., Mayberry, K. D., Telange, R., Sweileh, R. B. A., Dudley, M., Westbrook, C., et al. (2023) · Blood · doi:10.1182/blood.2022017265 · Cited by 22

Modulation of Cell Death in Age-Related Diseases

Tezil, T., & Başağa, H. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113196660702 · Cited by 21

Targeting Metabolism and Autophagy in the Context of Haematologic Malignancies

Banerji, V., & Gibson, S. B. (2012) · International Journal of Cell Biology · doi:10.1155/2012/595976 · Cited by 20

Neurodegenerative diseases: model organisms, pathology and autophagy

Suresh, S., Verma, V., Sateesh, S., Clement, J. P., & Manjithaya, R. R. (2018) · Journal of Genetics · doi:10.1007/s12041-018-0955-3 · Cited by 22

Association of single nucleotide autophagy‐related protein 5 gene polymorphism rs2245214 with susceptibility to non–small cell lung cancer

Nikseresht, M., Shahverdi, M., Dehghani, M., Abidi, H., Mahmoudi, R., Ghalamfarsa, G., Manzouri, L., & Ghavami, S. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27467 · Cited by 21

Unc-51-like kinase (ULK) complex-independent autophagy induced by hypoxia

Feng, Y., Kang, H. H., Wong, P., Gao, M., Wang, P., & Jiang, X. (2018) · Protein & Cell · doi:10.1007/s13238-018-0584-x · Cited by 21

Tetrahydroxystilbene Glucoside Suppresses NAPDH Oxidative Stress to Mitigate Apoptosis and Autophagy Induced by Cerebral Ischemia/Reperfusion Injury in Mice

Feng, Y., Wei, X., Dong, L., Hu, X., Huang, D., & Wang, K. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/3913981 · Cited by 21

The inducible amphisome isolates viral hemagglutinin and defends against influenza A virus infection

Omi, J., Watanabe‐Takahashi, M., Igai, K., Shimizu, E., Tseng, C.-Y., Miyasaka, T., Waku, T., Hama, S., Nakanishi, R., Goto, Y., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-13974-w · Cited by 21

The Role of WIPI2, ATG16L1 and ATG12-ATG5 in Selective and Nonselective Autophagy

Campisi, D., Hawkins, N., Bonjour, K., & Wollert, T. (2025) · Journal of Molecular Biology · doi:10.1016/j.jmb.2025.169138 · Cited by 22

ULK1 affects cell viability of goat Sertoli cell by modulating both autophagy and apoptosis

Pang, J., Han, L., Liu, Z.-F., Zheng, J., Zhao, J., Deng, K.-P., Wang, F., & Zhang, Y.-L. (2019) · In vitro Cellular & Developmental Biology-Animal · doi:10.1007/s11626-019-00371-2 · Cited by 15

Role of macrophage autophagy in atherosclerosis: modulation by bioactive compounds

Zahid, M. K., Sufian, H. B., Choudhury, M., Yamasaki, M., Al‐Harrasi, A., Moustaïd‐Moussa, N., & Rahman, S. M. (2021) · Biochemical Journal · doi:10.1042/bcj20200894 · Cited by 20

Polymerase delta-interacting protein 2 regulates collagen accumulation via activation of the Akt/mTOR pathway in vascular smooth muscle cells

Fujii, M., Amanso, A. M., Abrahão, T. B., Lassegue, B. P., & Griendling, K. K. (2016) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2016.01.016 · Cited by 20

Tauopathies: Mechanisms and Therapeutic Strategies

Tan, C., Zhang, X.-Y., Tan, L., & Yu, J. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170187 · Cited by 21

miR‐26a suppresses autophagy in swine Sertoli cells by targeting ULK2

Ran, M.-L., Li, Z., Cao, R., Weng, B., Peng, F.-Z., He, C., & Chen, B. (2018) · Reproduction in domestic animals = Zuchthygiene · doi:10.1111/rda.13177 · Cited by 21

Vps34-mediated macropinocytosis in Tuberous Sclerosis Complex 2-deficient cells supports tumorigenesis

Filippakis, H., Belaïd, A., Siroky, B. J., Wu, C., Alesi, N., Hougard, T. R., Nijmeh, J., Lam, H. C., & Henske, E. P. (2018) · Scientific Reports · doi:10.1038/s41598-018-32256-x · Cited by 19

Scaffold proteins in bulk and selective autophagy

Eickhorst, C., Licheva, M., & Kraft, C. (2020) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2020.01.009 · Cited by 22

Autophagy and the nutritional signaling pathway

He, L., Eslamfam, S., Ma, X., & Li, D. (2016) · Frontiers of Agricultural Science and Engineering · doi:10.15302/j-fase-2016106 · Cited by 20

The interplay of microRNAs and transcription factors in autophagy regulation in nonalcoholic fatty liver disease

Kim, Y., Lee, D.-H., Park, S., Jeon, T., & Jung, C. H. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00611-0 · Cited by 19

Protein Quality Control at the Sarcomere: Titin Protection and Turnover and Implications for Disease Development

Kötter, S., & Krüger, M. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.914296 · Cited by 22

Forkhead box protein A2 alleviates toll-like receptor 4-mediated inflammation, endoplasmic reticulum stress, autophagy, and apoptosis induced by lipopolysaccharide in bovine hepatocytes.

Xie, W., Xue, Y., Song, X., Zhang, H., Chang, G., & Shen, X.-Z. (2022) · Journal of Dairy Science · doi:10.3168/jds.2022-22252 · Cited by 17

Role of O-linked N-acetylglucosamine protein modification in oxidative stress-induced autophagy: a novel target for bone remodeling

Li, S., Ren, W., Zheng, J., Li, S., Zhi, K., & Gao, L. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01734-3 · Cited by 21

Molecular mechanism of hepatic steatosis: pathophysiological role of autophagy

Wang, K. (2016) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2016.14 · Cited by 19

Serine/Threonine Kinase Unc-51-like Kinase-1 (Ulk1) Phosphorylates the Co-chaperone Cell Division Cycle Protein 37 (Cdc37) and Thereby Disrupts the Stability of Cdc37 Client Proteins

Li, R., Yuan, F., Fu, W., Zhang, L., Zhang, N., Wang, Y., Ma, K., Li, X., Wang, L., Zhu, W.-G., et al. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.762443 · Cited by 19

Saturated hydrogen saline ameliorates lipopolysaccharide-induced acute lung injury by reducing excessive autophagy (Review)

Liu, Y., & Zhang, J. (2017) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2017.4353 · Cited by 19

Evaluation of cell damage induced by irradiated Zinc-Phthalocyanine-gold dendrimeric nanoparticles in a breast cancer cell line

Mfouo-Tynga, I. S., Houreld, N. N., & Abrahamse, H. (2018) · Biomedical Journal · doi:10.1016/j.bj.2018.05.002 · Cited by 19

Notch pathway: a bistable inducer of biological noise?

Vujovic, F., Hunter, N., & Farahani, R. H. (2019) · Cell Communication and Signaling · doi:10.1186/s12964-019-0453-0 · Cited by 18

The ULK1/2 and AMPK Inhibitor SBI-0206965 Blocks AICAR and Insulin-Stimulated Glucose Transport

Knudsen, J. R., Madsen, A. B., Persson, K. W., Henríquez‐Olguín, C., Li, Z., & Jensen, T. E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072344 · Cited by 19

The Protein Factor-arrest 11 (Far11) Is Essential for the Toxicity of Human Caspase-10 in Yeast and Participates in the Regulation of Autophagy and the DNA Damage Signaling

Lisa-Santamaría, P., Jiménez, A., & Revuelta, J. L. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.344192 · Cited by 18

Extracellular pH regulates autophagy via the AMPK–ULK1 pathway in rat cardiomyocytes

Zhao, L., Cui, L., Jiang, X., Zhang, J., Zhu, M., Jia, J., Zhang, Q., Zhang, J., Zhang, D., & Huang, Y. (2016) · FEBS Letters · doi:10.1002/1873-3468.12359 · Cited by 19

Dormancy, Quiescence, and Diapause: Savings Accounts for Life

Ozguldez, H. O., & Bulut-Karslıoğlu, A. (2024) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-112122-022528 · Cited by 17

Nanomedicine Approaches for Autophagy Modulation in Cancer Therapy

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In Vitro Screening Platforms for Identifying Autophagy Modulators in Mammalian Cells

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