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The machinery of macroautophagy
Open accessAbstract
Autophagy is a primarily degradative pathway that takes place in all eukaryotic cells. It is used for recycling cytoplasm to generate macromolecular building blocks and energy under stress conditions, to remove superfluous and damaged organelles to adapt to changing nutrient conditions and to maintain cellular homeostasis. In addition, autophagy plays a critical role in cytoprotection by preventing the accumulation of toxic proteins and through its action in various aspects of immunity including the elimination of invasive microbes and its participation in antigen presentation. The most prevalent form of autophagy is macroautophagy, and during this process, the cell forms a double-membrane sequestering compartment termed the phagophore, which matures into an autophagosome. Following delivery to the vacuole or lysosome, the cargo is degraded and the resulting macromolecules are released back into the cytosol for reuse. The past two decades have resulted in a tremendous increase with regard to the molecular studies of autophagy being carried out in yeast and other eukaryotes. Part of the surge in interest in this topic is due to the connection of autophagy with a wide range of human pathophysiologies including cancer, myopathies, diabetes and neurodegenerative disease. However, there are still many aspects of autophagy that remain unclear, including the process of phagophore formation, the regulatory mechanisms that control its induction and the function of most of the autophagy-related proteins. In this review, we focus on macroautophagy, briefly describing the discovery of this process in mammalian cells, discussing the current views concerning the donor membrane that forms the phagophore, and characterizing the autophagy machinery including the available structural information.
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“ATG7 is strictly required for autophagosome formation; it is an E1-like activating enzyme present in ubiquitin-like conjugation systems that promotes both cleavage and lipidation of LC3 and GABARAP [43].”
From A gene toolbox for monitoring autophagy transcription (2021) · cites this paper as [43]
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“ULK1 is considered as the master regulator of autophagy induction, triggering a cascade of signals, through direct phosphorylation of ATG proteins, that culminate in autophagosome formation [3, 43].”
From A gene toolbox for monitoring autophagy transcription (2021) · cites this paper as [43]
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“Indeed, autophagy functions as a quality control mechanism, maintaining cellular homeostasis by destroying aggregate-prone proteins and damaged organelles [45].”
From Unlocking the Therapeutic Potential of Medicinal Plants for Alzheimer’s Disease: Preclinical to Clinical Trial Insights (2023) · cites this paper as [45]
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Cites
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
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., & Shimizu, N. (1998) · Nature · doi:10.1038/33416 · Cited by 5,227
Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue
Duve, C. D., Pressman, B. C., Gianetto, R., Wattiaux, R., & Appelmans, F. (1955) · Biochemical Journal · doi:10.1042/bj0600604 · Cited by 4,176
Autophagy: process and functionPreprint
Mizushima, N. (2007) · Genes & Development · doi:10.1101/gad.1599207 · Cited by 4,104
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
Valente, E. M., Abou-Sleiman, P. M., Caputo, V., Muqit, M. M. K., Harvey, K., Gispert, S., Ali, Z., Del Turco, D., Bentivoglio, A. R., Healy, D. G., et al. (2004) · Science · doi:10.1126/science.1096284 · Cited by 3,481
Induction of autophagy and inhibition of tumorigenesis by beclin 1
Liang, X. H., Jackson, S., Seaman, M., Brown, K., Kempkes, B., Hibshoosh, H., & Levine, B. (1999) · Nature · doi:10.1038/45257 · Cited by 3,347
Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273
de Duve, C., & Wattiaux, R. (1966) · Annual Review of Physiology · doi:10.1146/annurev.ph.28.030166.002251 · Cited by 3,033
The Role of Atg Proteins in Autophagosome Formation
Mizushima, N., Yoshimori, T., & Ohsumi, Y. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154005 · Cited by 2,978
Autophagy in Health and Disease: A Double-Edged Sword
Shintani, T., & Klionsky, D. J. (2004) · Science · doi:10.1126/science.1099993 · Cited by 2,559
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Role of ERLINs in the Control of Cell Fate through Lipid Rafts
Manganelli, V., Longo, A., Mattei, V., Recalchi, S., Riitano, G., Caissutti, D., Capozzi, A., Sorice, M., Misasi, R., & Garofalo, T. (2021) · Cells · doi:10.3390/cells10092408 · Cited by 46
Lee, J., Xu, Y., Saidi, L. F., Xu, M., Zinsmaier, K. E., & Ye, Y. (2022) · Autophagy · doi:10.1080/15548627.2022.2065618 · Cited by 43
The role of protein acetylation in carcinogenesis and targeted drug discovery
Yang, J., Song, C., & Zhan, X. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.972312 · Cited by 42
Aveic, S., & Tonini, G. P. (2016) · Cancer Cell International · doi:10.1186/s12935-016-0341-2 · Cited by 44
Li, H., Tang, Y., Wen, L., Kong, X., Chen, X., Liu, P., Zhou, Z., Chen, W., Xiao, C., Xiao, P., et al. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.01.180 · Cited by 42
Prenatal alcohol exposure impairs autophagy in neonatal brain cortical microvessels
Girault, V., Gilard, V., Marguet, F., Lesueur, C., Hauchecorne, M., Ramdani, Y., Laquerrière, A., Marret, S., Jégou, S., Gonzalez, B. J., et al. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.29 · Cited by 46
Extracellular Collagen VI Has Prosurvival and Autophagy Instructive Properties in Mouse Fibroblasts
Castagnaro, S., Chrisam, M., Cescon, M., Braghetta, P., Grumati, P., & Bonaldo, P. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01129 · Cited by 42
Aqueous extract of clove inhibits tumor growth by inducing autophagy through AMPK/ULK pathway
Li, C., Xu, H., Chen, X., Chen, J., Li, X., Qiao, G., Tian, Y., Yuan, R., Su, S., Liu, X., et al. (2019) · Phytotherapy Research · doi:10.1002/ptr.6367 · Cited by 42
Talebian, S., Daghagh, H., Yousefi, B., Özkul, Y., Ilkhani, K., Seif, F., & Alivand, M. R. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111309 · Cited by 45
Luo, H., Pi, J., Zhang, J., Yang, E., Xu, H., Luo, H., Shen, L., Peng, Y., Liu, G.-B., Song, C., et al. (2021) · Clinical & Translational Immunology · doi:10.1002/cti2.1254 · Cited by 43
The pleiotropic roles of autophagy in Alzheimer’s disease: From pathophysiology to therapy
Festa, B. P., Barbosa, A. D., Rob, M., & Rubinsztein, D. C. (2021) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2021.07.011 · Cited by 41
Functional Amino Acids and Autophagy: Diverse Signal Transduction and Application
Liu, C., Ji, L., Hu, J., Zhao, Y., Johnston, L. J., Zhang, X., & Ma, X. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111427 · Cited by 44
The hunger strikes back: an epigenetic memory for autophagy
González-Rodríguez, P., Füllgrabe, J., & Joseph, B. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01159-4 · Cited by 44
Programmed cell death in tumor immunity: mechanistic insights and clinical implications
Wang, M., Yu, F., Zhang, Y., & Li, P. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1309635 · Cited by 43
Kobayashi, H., Imanaka, S., Yoshimoto, C., Matsubara, S., & Shigetomi, H. (2024) · Reproductive Medicine and Biology · doi:10.1002/rmb2.12577 · Cited by 41
Autophagy-lysosomal pathway impairment and cathepsin dysregulation in Alzheimer’s disease
Mançano, A. S. F., Pina, J. G., Froes, B. R., & Sciani, J. M. (2024) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2024.1490275 · Cited by 51
Hernández, C., Barrachina, M. D., Vallecillo-Hernández, J., Álvarez, Á., Ortiz‐Masiá, D., Cosín‐Roger, J., Esplugues, J. V., & Calatayud, S. (2015) · Journal of Gastroenterology · doi:10.1007/s00535-015-1137-1 · Cited by 41
Avoidance and Subversion of Eukaryotic Homeostatic Autophagy Mechanisms by Bacterial Pathogens
Miller, C. N., & Celli, J. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.07.007 · Cited by 42
Immunity to uropathogens: the emerging roles of inflammasomes
Hamilton, C., Tan, L., Miethke, T., & Anand, P. (2017) · Nature Reviews Urology · doi:10.1038/nrurol.2017.25 · Cited by 40
The role of Runx2 in facilitating autophagy in metastatic breast cancer cells
Tandon, M., Othman, A. H., Ashok, V., Stein, G. S., & Pratap, J. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25916 · Cited by 42
ELMO1 Regulates Autophagy Induction and Bacterial Clearance During Enteric Infection
Sarkar, A., Tindle, C., Pranadinata, R. F., Reed, S. L., Eckmann, L., Stappenbeck, T. S., Ernst, P. B., & Das, S. (2017) · The Journal of Infectious Diseases · doi:10.1093/infdis/jix528 · Cited by 42
Structure and function of yeast Atg20, a sorting nexin that facilitates autophagy induction
Popelka, H., Damasio, A., Hinshaw, J. E., Klionsky, D. J., & Ragusa, M. J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1708367114 · Cited by 42
Ramadan, A., Singh, K. K., Quan, A., Plant, P. J., Al-Omran, M. A., Teoh, H., & Verma, S. (2017) · Journal of Vascular Surgery · doi:10.1016/j.jvs.2017.08.086 · Cited by 41
The Pat1-Lsm Complex Stabilizes ATG mRNA during Nitrogen Starvation-Induced Autophagy
Gatica, D., Hu, G., Liu, X., Zhang, N., Williamson, P. R., & Klionsky, D. J. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.11.002 · Cited by 41
The Role of the Interplay Between Autophagy and NLRP3 Inflammasome in Metabolic Disorders
Lv, S., Wang, H., & Li, X. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.634118 · Cited by 42
Research Progress on the Functions and Mechanism of circRNA in Cisplatin Resistance in Tumors
Mu, Q., Lv, Y., Luo, C., Liu, X., Huang, C., Xiu, Y., & Tang, L. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.709324 · Cited by 41
Mitochondrial Quality Control in Cardiac-Conditioning Strategies against Ischemia-Reperfusion Injury
García‐Niño, W. R., Zazueta, C., Buelna‐Chontal, M., & Silva‐Palacios, A. (2021) · Life · doi:10.3390/life11111123 · Cited by 42
Li, J., & Gong, X. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.820071 · Cited by 41
V-ATPase recruitment to ER exit sites switches COPII-mediated transport to lysosomal degradation
Sun, Y., Wang, X., Yang, X., Wang, L., Ding, J., Wang, C.-C., Zhang, H., & Wang, X. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.10.007 · Cited by 42
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Basak, B., & Holzbaur, E. L. F. (2025) · Journal of Molecular Biology · doi:10.1016/j.jmb.2025.169161 · Cited by 44
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Cheong, H. (2015) · Archives of Pharmacal Research · doi:10.1007/s12272-015-0562-2 · Cited by 40
Jin, X., Li, F., Zheng, X., Liu, Y., Hirayama, R., Liu, X., Li, P., Zhao, T., Dai, Z., & Li, Q. (2015) · Scientific Reports · doi:10.1038/srep13815 · Cited by 40
Autophagy: A brief overview in perspective of dermatology
Nagar, R. (2016) · Indian Journal of Dermatology Venereology and Leprology · doi:10.4103/0378-6323.196320 · Cited by 41
Autophagy and Age-Related Eye Diseases
Yang, X., Pan, X., Zhao, X., Jin, L., Xu, M., Bai, D., Hu, Y., Liu, X., Yu, Q., & Gao, D. (2019) · BioMed Research International · doi:10.1155/2019/5763658 · Cited by 40
Golgi-associated Rab GTPases implicated in autophagy
Lu, Q., Wang, P., & Yang, L. (2021) · Cell & Bioscience · doi:10.1186/s13578-021-00543-2 · Cited by 41
Molecular Mechanism and Regulation of Autophagy and Its Potential Role in Epilepsy
Zhu, H., Wang, W., & Li, Y. (2022) · Cells · doi:10.3390/cells11172621 · Cited by 44
The role of lncRNA H19 in tumorigenesis and drug resistance of human Cancers
Zhang, X., Luo, M., Zhang, J., Guo, B., Singh, S., Lin, X., Xiong, H., Ju, S., Wang, L., Zhou, Y., et al. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.1005522 · Cited by 40
Mishra, J., Bhatti, G. K., Sehrawat, A., Singh, C., Singh, A., Reddy, A. P., Reddy, P. H., & Bhatti, J. S. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.121153 · Cited by 38
Zhao, W., Fan, C.-L., Hu, X., Ban, X.-X., Wan, H., He, Y., Zhāng, Q., & Xiong, K. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01373-1 · Cited by 44
Wang, S., Zhang, K., Song, X.-T., Huang, Q., Lin, S., Deng, S., Qi, M.-Y., Yang, Y., Lu, Q., Zhao, D., et al. (2023) · Cells · doi:10.3390/cells12131769 · Cited by 46
Autophagy/Mitophagy in Airway Diseases: Impact of Oxidative Stress on Epithelial Cells
Albano, G. D., Montalbano, A. M., Gagliardo, R. P., & Profita, M. (2023) · Biomolecules · doi:10.3390/biom13081217 · Cited by 41
Autophagy-modulating biomaterials: multifunctional weapons to promote tissue regeneration
Wu, Y. F., Li, L., Ning, Z., Li, C., Yin, Y., Chen, K., Li, L., Xu, F., & Gao, J. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-023-01346-3 · Cited by 38
Wang, X., Yang, J., Yang, W., Sheng, H., Jia, B., Peng, C., Xu, S., Hong, X., Jiang, C., Yang, Y., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.10.026 · Cited by 46
Yang, N., Lai, Y., Yu, G., Zhang, X., Shi, J., Xiang, L., Zhang, J., Wu, Y., Jiang, X., Zhang, X., et al. (2025) · Autophagy · doi:10.1080/15548627.2025.2493455 · Cited by 40
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Pérez-Martín, M., Blaby, C., Pérez‐Pérez, M. E., Andrés-Garrido, A., Blaby, I. K., Merchant, S., & Crespo, J. L. (2015) · Eukaryotic Cell · doi:10.1128/ec.00081-15 · Cited by 39
A systematic view on E3 ligase Ring TRIMmers with a focus on cardiac function and disease
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Colella, B., Faienza, F., Carinci, M., D’Alessandro, G., Catalano, M., Santoro, A., Cecconi, F., Limatola, C., & Bartolomeo, S. D. (2018) · Cellular Signalling · doi:10.1016/j.cellsig.2018.10.017 · Cited by 39
Carvacrol reduces adipogenic differentiation by modulating autophagy and ChREBP expression
Spalletta, S., Flati, V., Toniato, E., Gregorio, J. D., Marino, A., Pierdomenico, L., Marchisio, M., D’Orazi, G., Cacciatore, I., & Robuffo, I. (2018) · PLoS ONE · doi:10.1371/journal.pone.0206894 · Cited by 39
Atg11 is required for initiation of glucose starvation-induced autophagy
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Wang, X., Sun, Y., Peng, X., Naqvi, S. M. A. S., Yang, Y., Zhang, J., Chen, M., Chen, Y., Chen, H., Yan, H., et al. (2020) · Cancer Control · doi:10.1177/1073274820976664 · Cited by 40
Maneiro, M., Vita, E. D., Conole, D., Kounde, C. S., Zhang, Q., & Tate, E. W. (2021) · Progress in medicinal chemistry · doi:10.1016/bs.pmch.2021.01.002 · Cited by 38
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Martelli, A., Omrani, M., Zarghooni, M., Citi, V., Brogi, S., Calderone, V., Sureda, A., Lorzadeh, S., Rosa, S. C. D. S., Grabarek, B. O., et al. (2022) · Cancers · doi:10.3390/cancers14235839 · Cited by 40
Yu, X., Zhao, Z., & Jiang, Z. (2022) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjac042 · Cited by 38
Yi, F., Cai, C., Ruan, B., Hao, M., Yeo, S. K., Haas, M., Yang, F., Zhang, X., & Guan, J. (2022) · Autophagy · doi:10.1080/15548627.2022.2148432 · Cited by 39
Inhibition of autophagy; an opportunity for the treatment of cancer resistance
Tonkin-Reeves, A., Giuliani, C. M., & Price, J. T. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1177440 · Cited by 41
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Gewirtz, D. A. (2014) · Radiation Research · doi:10.1667/rr13774.1 · Cited by 38
Polak, A., Kiliszek, P., Sewastianik, T., Szydłowski, M., Jabłońska, E., Białopiotrowicz, E., Górniak, P., Markowicz, S., Nowak, E., Grygorowicz, M. A., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0155893 · Cited by 38
Ntsapi, C., Lumkwana, D., Swart, C., du Toit, A., & Loos, B. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.07.002 · Cited by 39
Exploiting Nanomaterial‐Mediated Autophagy for Cancer Therapy
Wei, W., Rosenkrans, Z. T., Luo, Q., Lan, X., & Cai, W. (2018) · Small Methods · doi:10.1002/smtd.201800365 · Cited by 41
Wang, Y., Huang, H., Jin, Y., Shen, K., Chen, X., Xu, Z., Jin, B., & Pan, H. (2019) · Food and Chemical Toxicology · doi:10.1016/j.fct.2019.110591 · Cited by 38
Endicott, S. J., Boynton, D. N., Beckmann, L. J., & Miller, R. A. (2020) · Autophagy · doi:10.1080/15548627.2020.1725378 · Cited by 38
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Gray, J. P., Uddin, M. N., Chaudhari, R. R., Sutton, M. N., Yang, H., Rask, P. J., Locke, H., Engel, B. J., Batistatou, N., Wang, J., et al. (2021) · Chemical Science · doi:10.1039/d0sc03603j · Cited by 38
Caloric restriction mimetics for the treatment of cardiovascular diseases
Sciarretta, S., Forte, M., Castoldi, F., Frati, G., Versaci, F., Sadoshima, J., Kroemer, G., & Maiuri, M. C. (2020) · Cardiovascular Research · doi:10.1093/cvr/cvaa297 · Cited by 39
G‐quadruplex regulation of neural gene expression
Cave, J. W., & Willis, D. E. (2021) · FEBS Journal · doi:10.1111/febs.15900 · Cited by 37
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Wen, X., Yang, Y., & Klionsky, D. J. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.100966 · Cited by 39
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Wei, Z. J., Hu, X., Wu, Y., Zhou, L., Zhao, M., & Lin, Q. (2024) · Biomolecules · doi:10.3390/biom14121517 · Cited by 37
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Delorme‐Axford, E., Morosky, S. A., Bomberger, J. M., Stolz, D. B., Jackson, W. T., & Coyne, C. B. (2014) · mBio · doi:10.1128/mbio.02147-14 · Cited by 37
REDD1 attenuates cardiac hypertrophy via enhancing autophagy
Liu, C., Xue, R., Wu, D., Wu, L., Chen, C., Tan, W., Chen, Y., & Dong, Y. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.10.079 · Cited by 37
Regulation of peroxisome dynamics by phosphorylation
Oeljeklaus, S., Schummer, A., Mastalski, T., Platta, H. W., & Warscheid, B. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.12.022 · Cited by 38
Ryabovol, V., & Minibayeva, F. V. (2016) · Biochemistry (Moscow) · doi:10.1134/s0006297916040052 · Cited by 37
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Autophagy‐dependent regulation of MHC‐I molecule presentation
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Metadata
- Authors
- Feng, Y., He, D., Yao, Z., & Klionsky, D. J.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Klionsky, Daniel J
- Venue
- Cell Research
- Published
- 2013-12-24
- Volume
- 24
- Issue
- 1
- Pages
- 24-41
- ISSN
- 1001-0602 (ISSN-L)
- 1748-7838
- PMC
- PMC3879710
- OpenAlex
- W2044621729
- Cited by
- 2,083
- References
- 180
- Citations by year
- 2026: 84 · 2025: 130 · 2024: 193 · 2023: 180 · 2022: 238 · 2021: 215 · 2020: 200 · 2019: 185 · 2018: 177 · 2017: 161 · 2016: 161 · 2015: 109 · 2014: 45 · 2013: 3
- FWCI
- 12.56
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cell Research (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM053396)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- macroautophagy, autophagy machinery, phagophore formation, autophagosomes, autophagy-related proteins, autophagy regulation, lysosomes, cellular homeostasis, cytoprotection, neurodegenerative diseases, cancer, yeast autophagy
- MeSH terms
- Animals, Autophagy, Homeostasis, Humans, Lysosomes, Phagosomes, Pichia, Saccharomyces cerevisiae, Vacuoles, Protein Serine-Threonine Kinases
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