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The Atg1–kinase complex tethers Atg9-vesicles to initiate autophagy
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471140864.ps0521s52openalex-snapshot
Recombinant Protein Complex Expression in E. coli
inferredcites →https://doi.org/10.1002/bies.201200130openalex-snapshot
Endocytosis and autophagy: Shared machinery for degradation
inferredcites →https://doi.org/10.1002/yea.1142openalex-snapshot
A versatile toolbox for PCR‐based tagging of yeast genes: new fluorescent proteins, more markers and promoter substitution cassettes
inferredcites →https://doi.org/10.1006/bbrc.1995.1636openalex-snapshot
Novel System for Monitoring Autophagy in the Yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0014-5793(93)80398-eopenalex-snapshot
Isolation and characterization of autophagy‐defective mutants of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0014-5793(94)00672-5openalex-snapshot
Isolation of autophagocytosis mutants of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/j.bbrc.2009.09.034openalex-snapshot
Characterization of the Atg17–Atg29–Atg31 complex specifically required for starvation-induced autophagy in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/j.ceb.2009.11.014openalex-snapshot
Mammalian autophagy: core molecular machinery and signaling regulation
inferredcites →https://doi.org/10.1016/j.cell.2012.11.028openalex-snapshot
Architecture of the Atg17 Complex as a Scaffold for Autophagosome Biogenesis
inferredcites →https://doi.org/10.1016/j.pep.2009.01.002openalex-snapshot
The titerless infected-cells preservation and scale-up (TIPS) method for large-scale production of NO-sensitive human soluble guanylate cyclase (sGC) from insect cells infected with recombinant baculovirus
inferredcites →https://doi.org/10.1021/bi00504a006openalex-snapshot
Estimation of globular protein secondary structure from circular dichroism
inferredcites →https://doi.org/10.1038/nbt.1511openalex-snapshot
MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
inferredcites →https://doi.org/10.1038/nrm3696openalex-snapshot
The autophagosome: origins unknown, biogenesis complex
inferredcites →https://doi.org/10.1038/nsmb.2822openalex-snapshot
Structural basis of starvation-induced assembly of the autophagy initiation complex
inferredcites →https://doi.org/10.1042/bj20071427openalex-snapshot
The regulation and function of Class III PI3Ks: novel roles for Vps34
inferredcites →https://doi.org/10.1056/nejmra1205406openalex-snapshot
Autophagy in Human Health and Disease
inferredcites →https://doi.org/10.1073/pnas.0903316106openalex-snapshot
The Tor and PKA signaling pathways independently target the Atg1/Atg13 protein kinase complex to control autophagy
inferredcites →https://doi.org/10.1073/pnas.1300064110openalex-snapshot
Atg29 phosphorylation regulates coordination of the Atg17-Atg31-Atg29 complex with the Atg11 scaffold during autophagy initiation
inferredcites →https://doi.org/10.1073/pnas.1407214111openalex-snapshot
Assembly and dynamics of the autophagy-initiating Atg1 complex
inferredcites →https://doi.org/10.1073/pnas.1421092112openalex-snapshot
Atg13 HORMA domain recruits Atg9 vesicles during autophagosome formation
inferredcites →https://doi.org/10.1074/jbc.271.30.17621openalex-snapshot
Genetic and Phenotypic Overlap between Autophagy and the Cytoplasm to Vacuole Protein Targeting Pathway
inferredcites →https://doi.org/10.1080/15548627.2015.1040972openalex-snapshot
Molecular interactions of theSaccharomyces cerevisiaeAtg1 complex provide insights into assembly and regulatory mechanisms
inferredcites →https://doi.org/10.1083/jcb.150.6.1507openalex-snapshot
Tor-Mediated Induction of Autophagy via an Apg1 Protein Kinase Complex
inferredcites →https://doi.org/10.1083/jcb.200711112openalex-snapshot
Quantitative analysis of autophagy-related protein stoichiometry by fluorescence microscopy
inferredcites →https://doi.org/10.1083/jcb.200712064openalex-snapshot
FIP200, a ULK-interacting protein, is required for autophagosome formation in mammalian cells
inferredcites →https://doi.org/10.1083/jcb.200912089openalex-snapshot
An Atg9-containing compartment that functions in the early steps of autophagosome biogenesis
inferredcites →https://doi.org/10.1083/jcb.201202061openalex-snapshot
Atg9 vesicles are an important membrane source during early steps of autophagosome formation
inferredcites →https://doi.org/10.1091/mbc.e04-08-0669openalex-snapshot
Atg17 Functions in Cooperation with Atg1 and Atg13 in Yeast Autophagy
inferredcites →https://doi.org/10.1091/mbc.e04-10-0894openalex-snapshot
Atg17 Regulates the Magnitude of the Autophagic Response
inferredcites →https://doi.org/10.1091/mbc.e06-07-0612openalex-snapshot
Atg27 Is Required for Autophagy-dependent Cycling of Atg9
inferredcites →https://doi.org/10.1091/mbc.e07-10-1048openalex-snapshot
Organization of the Pre-autophagosomal Structure Responsible for Autophagosome Formation
inferredcites →https://doi.org/10.1091/mbc.e08-05-0544openalex-snapshot
Self-Interaction Is Critical for Atg9 Transport and Function at the Phagophore Assembly Site during Autophagy
inferredcites →https://doi.org/10.1091/mbc.e08-12-1248openalex-snapshot
Nutrient-dependent mTORC1 Association with the ULK1–Atg13–FIP200 Complex Required for Autophagy
inferredcites →https://doi.org/10.1091/mbc.e08-12-1249openalex-snapshot
ULK-Atg13-FIP200 Complexes Mediate mTOR Signaling to the Autophagy Machinery
inferredcites →https://doi.org/10.1093/jb/mvt012openalex-snapshot
MIT domain of Vps4 is a Ca2+-dependent phosphoinositide-binding domain
inferredcites →https://doi.org/10.1110/ps.03258404openalex-snapshot
On the analysis of membrane protein circular dichroism spectra
inferredcites →https://doi.org/10.1111/j.1365-2443.2007.01050.xopenalex-snapshot
Hierarchy of Atg proteins in pre‐autophagosomal structure organization
inferredcites →https://doi.org/10.1111/j.1365-2443.2008.01188.xopenalex-snapshot
Transport of phosphatidylinositol 3‐phosphate into the vacuole via autophagic membranes in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1111/j.1365-2443.2009.01299.xopenalex-snapshot
Atg17 recruits Atg9 to organize the pre‐autophagosomal structure
inferredcites →https://doi.org/10.1128/mcb.01344-09openalex-snapshot
Tor Directly Controls the Atg1 Kinase Complex To Regulate Autophagy
inferredcites →https://doi.org/10.1186/1472-6750-13-12openalex-snapshot
A new method to customize protein expression vectors for fast, efficient and background free parallel cloning
inferredcites →https://doi.org/10.1242/jcs.03172openalex-snapshot
Starvation and ULK1-dependent cycling of mammalian Atg9 between the TGN and endosomes
inferredcites →https://doi.org/10.1242/jcs.122960openalex-snapshot
Fine mapping of autophagy-related proteins during autophagosome formation in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1534/genetics.110.116566openalex-snapshot
Autophosphorylation Within the Atg1 Activation Loop Is Required for Both Kinase Activity and the Induction of Autophagy in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1534/genetics.112.149013openalex-snapshot
Autophagic Processes in Yeast: Mechanism, Machinery and Regulation
inferredcites →https://doi.org/10.3109/09687688.2013.850178openalex-snapshot
Location and membrane sources for autophagosome formation – from ER-mitochondria contact sites to Golgi-endosome-derived carriers
inferredcites →https://doi.org/10.4161/auto.25529openalex-snapshot
Temporal analysis of recruitment of mammalian ATG proteins to the autophagosome formation site
inferredcites →https://doi.org/10.4161/auto.25687openalex-snapshot
Structural characterization of theSaccharomyces cerevisiaeautophagy regulatory complex Atg17-Atg31-Atg29
inferredcites →https://doi.org/10.4161/auto.4129openalex-snapshot
A Cycling Protein Complex Required for Selective Autophagy
inferredcites →https://doi.org/10.4161/auto.6.8.13849openalex-snapshot
Activation of Atg1 kinase in autophagy by regulated phosphorylation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4793027openalex-extracted
Intricacies of Lipid Supply in Autophagic Membrane Expansion
inferred← citeshttps://doi.org/10.1002/1873-3468.14717openalex-snapshot
The role of the HORMA domain proteins ATG13 and ATG101 in initiating autophagosome biogenesis
inferred← citeshttps://doi.org/10.1002/1873-3468.14741openalex-snapshot
Nutrient‐dependent signaling pathways that control autophagy in yeast
inferred← citeshttps://doi.org/10.1002/jcp.30819openalex-snapshot
Expanding the view of the molecular mechanisms of autophagy pathway
inferred← citeshttps://doi.org/10.1002/jlb.3ma0218-070ropenalex-snapshot
Cellular and molecular mechanisms involved in the resolution of innate leukocyte inflammation
inferred← citeshttps://doi.org/10.1002/ptr.8103openalex-snapshot
Natural products targeting macroautophagy signaling in hepatocellular carcinoma therapy: Recent evidence and perspectives
inferred← citeshttps://doi.org/10.1007/978-1-4939-8873-0_6openalex-snapshot
Reconstituting Autophagy Initiation from Purified Components
inferred← citeshttps://doi.org/10.1007/978-981-15-0602-4_2openalex-snapshot
Regulation of ATG and Autophagy Initiation
inferred← citeshttps://doi.org/10.1007/978-981-16-2830-6_14openalex-snapshot
Cell Models in Autophagy Research
inferred← citeshttps://doi.org/10.1007/978-981-16-2830-6_2openalex-snapshot
Autophagosomal Membrane Origin and Formation
inferred← citeshttps://doi.org/10.1007/s00018-016-2224-zopenalex-snapshot
Regulation of actin nucleation and autophagosome formation
inferred← citeshttps://doi.org/10.1007/s00441-016-2472-0openalex-snapshot
Roles of mitophagy in cellular physiology and development
inferred← citeshttps://doi.org/10.1007/s41745-016-0015-zopenalex-snapshot
Multifaceted Housekeeping Functions of Autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-822003-0.00013-9openalex-snapshot
Mechanisms of autophagy: the machinery of macroautophagy and points of control
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2017.07.001openalex-snapshot
Membrane Trafficking in Autophagy
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2026.07.002openalex-snapshot
Understanding autophagy: A molecular and physiological perspective
inferred← citeshttps://doi.org/10.1016/bs.mie.2016.09.085openalex-snapshot
Monitoring the Formation of Autophagosomal Precursor Structures in Yeast Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2020.01.009openalex-snapshot
Scaffold proteins in bulk and selective autophagy
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2020.03.002openalex-snapshot
Dancing while self-eating: Protein intrinsic disorder in autophagy
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119064openalex-snapshot
Small but mighty: Atg8s and Rabs in membrane dynamics during autophagy
inferred← citeshttps://doi.org/10.1016/j.bbamem.2021.183731openalex-snapshot
Molecular and mesoscopic geometries in autophagosome generation. A review
inferred← citeshttps://doi.org/10.1016/j.ceb.2021.02.001openalex-snapshot
Membrane supply and remodeling during autophagosome biogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.108972openalex-snapshot
Dihydroceramide Desaturase Regulates the Compartmentalization of Rac1 for Neuronal Oxidative Stress
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110702openalex-snapshot
Dimerization-dependent membrane tethering by Atg23 is essential for yeast autophagy
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113528openalex-snapshot
Apolipoproteins L1 and L3 control mitochondrial membrane dynamics
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2018.11.001openalex-snapshot
Membrane-binding domains in autophagy
inferred← citeshttps://doi.org/10.1016/j.cstres.2024.10.001openalex-snapshot
Ebeiedinone and peimisine inhibit cigarette smoke extract-induced oxidative stress injury and apoptosis in BEAS-2B cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.03.015openalex-snapshot
Crosstalk between the Secretory and Autophagy Pathways Regulates Autophagosome Formation
inferred← citeshttps://doi.org/10.1016/j.ecolind.2018.05.068openalex-snapshot
Characterization of twelve autophagy-related genes from yellow catfish Pelteobagrus fulvidraco and their transcriptional responses to waterborne zinc exposure
inferred← citeshttps://doi.org/10.1016/j.jare.2023.06.010openalex-snapshot
Autophagy, a double-edged sword for oral tissue regeneration
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101573openalex-snapshot
Mechanism of Atg9 recruitment by Atg11 in the cytoplasm-to-vacuole targeting pathway
inferred← citeshttps://doi.org/10.1016/j.jmb.2016.02.027openalex-snapshot
Mechanisms of Selective Autophagy in Normal Physiology and Cancer
inferred← citeshttps://doi.org/10.1016/j.jmb.2016.03.030openalex-snapshot
Regulation of Autophagy By Signaling Through the Atg1/ULK1 Complex
inferred← citeshttps://doi.org/10.1016/j.jmb.2016.10.029openalex-snapshot
Phospholipids in Autophagosome Formation and Fusion
inferred← citeshttps://doi.org/10.1016/j.jmb.2017.01.006openalex-snapshot
Sensing Membrane Curvature in Macroautophagy
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.06.017openalex-snapshot
Mechanistic Insights into the Role of Atg11 in Selective Autophagy
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.07.027openalex-snapshot
Recruitment and Activation of the ULK1/Atg1 Kinase Complex in Selective Autophagy
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.09.005openalex-snapshot
Mechanisms of Autophagy in Metabolic Stress Response
inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168489openalex-snapshot
The Role of ATG9 Vesicles in Autophagosome Biogenesis
inferred← citeshttps://doi.org/10.1016/j.jmb.2025.168954openalex-snapshot
The PKA Signaling Pathway Regulates the Association of the Autophagy Initiation Complex With the Lipidation Machinery
inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169138openalex-snapshot
The Role of WIPI2, ATG16L1 and ATG12-ATG5 in Selective and Nonselective Autophagy
inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169288openalex-snapshot
ATG9 Not Just an Autophagy Related Protein
inferred← citeshttps://doi.org/10.1016/j.jsb.2016.04.005openalex-snapshot
Insights into autophagosome biogenesis from in vitro reconstitutions
inferred← citeshttps://doi.org/10.1016/j.mex.2016.08.001openalex-snapshot
A re-usable wave bioreactor for protein production in insect cells
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.10.024openalex-snapshot
Multilayered regulation of autophagy by the Atg1 kinase orchestrates spatial and temporal control of autophagosome formation
inferred← citeshttps://doi.org/10.1016/j.sbi.2016.09.010openalex-snapshot
Structural biology of the core autophagy machinery
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.05.002openalex-snapshot
Autophagosome Biogenesis and the Endoplasmic Reticulum: A Plant Perspective
inferred← citeshttps://doi.org/10.1038/s41421-020-0161-3openalex-snapshot
Emerging roles of ATG proteins and membrane lipids in autophagosome formation
inferred← citeshttps://doi.org/10.1038/s41467-024-51402-wopenalex-snapshot
Palmitoylation of ULK1 by ZDHHC13 plays a crucial role in autophagy
inferred← citeshttps://doi.org/10.1038/s44318-025-00536-8openalex-snapshot
Soma-localized Rab39 inhibits synaptic autophagy by controlling trafficking of Atg9 vesicles
inferred← citeshttps://doi.org/10.1042/bst20200130openalex-snapshot
In vitro reconstitution of autophagic processes
inferred← citeshttps://doi.org/10.1042/bst20240015openalex-snapshot
Biogenesis of omegasomes and autophagosomes in mammalian autophagy
inferred← citeshttps://doi.org/10.1073/pnas.2005539118openalex-snapshot
Downregulation of autophagy by Met30-mediated Atg9 ubiquitination
inferred← citeshttps://doi.org/10.1073/pnas.2508391123openalex-snapshot
ATG9A-mediated plasma membrane repair is linked to Vps13A and regulated by glycosylation
inferred← citeshttps://doi.org/10.1080/15548627.2016.1277312openalex-snapshot
The molecular mechanism of Atg13 function in autophagy induction: What is hidden behind the data?
inferred← citeshttps://doi.org/10.1080/15548627.2017.1359381openalex-snapshot
Architecture of the ATG2B-WDR45 complex and an aromatic Y/HF motif crucial for complex formation
inferred← citeshttps://doi.org/10.1080/15548627.2017.1382782openalex-snapshot
Conserved and unique features of the fission yeast core Atg1 complex
inferred← citeshttps://doi.org/10.1080/15548627.2017.1387342openalex-snapshot
Systematic analysis of ATG13 domain requirements for autophagy induction
inferred← citeshttps://doi.org/10.1080/15548627.2018.1477382openalex-snapshot
Atg9 proteins, not so different after all
inferred← citeshttps://doi.org/10.1080/15548627.2019.1596478openalex-snapshot
RAB2 regulates the formation of autophagosome and autolysosome in mammalian cells
inferred← citeshttps://doi.org/10.1080/15548627.2019.1639300openalex-snapshot
Subnanometer resolution cryo-EM structure of Arabidopsis thaliana ATG9
inferred← citeshttps://doi.org/10.1080/15548627.2019.1648117openalex-snapshot
The carboxy terminus of yeast Atg13 binds phospholipid membrane via motifs that overlap with the Vac8-interacting domain
inferred← citeshttps://doi.org/10.1080/15548627.2021.1877934openalex-snapshot
Snx4-assisted vacuolar targeting of transcription factors defines a new autophagy pathway for controlling ATG expression
inferred← citeshttps://doi.org/10.1080/15548627.2021.1898749openalex-snapshot
Atg9-centered multi-omics integration reveals new autophagy regulators inSaccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1080/15548627.2021.1909407openalex-snapshot
Phosphoregulation of the autophagy machinery by kinases and phosphatases
inferred← citeshttps://doi.org/10.1080/15548627.2021.1934270openalex-snapshot
BECN2 (beclin 2) Negatively Regulates Inflammasome Sensors Through ATG9A-Dependent but ATG16L1- and LC3-Independent Non-Canonical Autophagy
inferred← citeshttps://doi.org/10.1080/15548627.2023.2175305openalex-snapshot
Autophagic structures revealed by cryo-electron tomography: new clues about autophagosome biogenesis
inferred← citeshttps://doi.org/10.1080/15548627.2024.2447206openalex-snapshot
The ER protein CANX (calnexin)-mediated autophagy protects against alzheimer disease
inferred← citeshttps://doi.org/10.1080/15548627.2024.2447207openalex-snapshot
Cargo hitchhiking autophagy – a hybrid autophagy pathway utilized in yeast
inferred← citeshttps://doi.org/10.1080/15548627.2025.2509376openalex-snapshot
S-palmitoylation coordinates the trafficking of ATG9A to mediate autophagy initiation
inferred← citeshttps://doi.org/10.1080/27694127.2023.2236407openalex-snapshot
Neurodegenerative disease-associated inclusion bodies are cleared by selective autophagy in budding yeast
inferred← citeshttps://doi.org/10.1080/27694127.2025.2555835openalex-snapshot
Revisiting the evolution of the yeast Atg1 complex
inferred← citeshttps://doi.org/10.1083/jcb.201710116openalex-snapshot
Atg9 establishes Atg2-dependent contact sites between the endoplasmic reticulum and phagophores
inferred← citeshttps://doi.org/10.1083/jcb.201802003openalex-snapshot
Modulation of the secretory pathway by amino-acid starvation
inferred← citeshttps://doi.org/10.1083/jcb.201812106openalex-snapshot
SNX3 drives maturation of Borrelia phagosomes by forming a hub for PI(3)P, Rab5a, and galectin-9
inferred← citeshttps://doi.org/10.1083/jcb.202002085openalex-snapshot
Autophagosome biogenesis: From membrane growth to closure
inferred← citeshttps://doi.org/10.1083/jcb.202107151openalex-snapshot
Cdc14 spatiotemporally dephosphorylates Atg13 to activate autophagy during meiotic divisions
inferred← citeshttps://doi.org/10.1093/abbs/gmaa031openalex-snapshot
A COPII subunit interacting with ER-phagy receptor: a new potential avenue to maintaining neuronal homeostasis
inferred← citeshttps://doi.org/10.1093/genetics/iyad154openalex-snapshot
Autophagy impairment and lifespan reduction caused by Atg1 RNAi or Atg18 RNAi expression in adult fruit flies (Drosophila melanogaster)
inferred← citeshttps://doi.org/10.1093/jxb/erx392openalex-snapshot
Lipids in membrane dynamics during autophagy in plants
inferred← citeshttps://doi.org/10.1093/jxb/erz515openalex-snapshot
Combating stress: the interplay between hormone signaling and autophagy in plants
inferred← citeshttps://doi.org/10.1101/2023.03.22.533865openalex-snapshot
Knockdown of Atg1 or Atg18 in adult adipocytes impairs lipophagy and reduces lifespan of fruit flies ( Drosophila melanogaster )
inferred← citeshttps://doi.org/10.1101/2025.06.27.661946openalex-snapshot
Influence of ULK1 activity on the memory of ATG101 auto-activation dynamics
inferred← citeshttps://doi.org/10.1101/2025.11.06.685569openalex-snapshot
A structural and regulatory framework for Atg9-containing vesicle formation and their Atg1-dependent remodelling during autophagy initiation
inferred← citeshttps://doi.org/10.1104/pp.17.01236openalex-snapshot
Dynamics of Autophagosome Formation
inferred← citeshttps://doi.org/10.1111/febs.13661openalex-snapshot
Autophagy in the test tube: In vitro reconstitution of aspects of autophagosome biogenesis
inferred← citeshttps://doi.org/10.1146/annurev-biochem-061516-044820openalex-snapshot
Mechanisms of Autophagy Initiation
inferred← citeshttps://doi.org/10.1146/annurev-biochem-090920-103246openalex-snapshot
Evolutionary Dynamics and Molecular Mechanisms of HORMA Domain Protein Signaling
inferred← citeshttps://doi.org/10.1155/2020/8865611openalex-snapshot
Autophagy and Redox Homeostasis in Parkinson’s: A Crucial Balancing Act
inferred← citeshttps://doi.org/10.1172/jci133283openalex-snapshot
Beclin 2 negatively regulates innate immune signaling and tumor development
inferred← citeshttps://doi.org/10.1177/25152564231183898openalex-snapshot
The Organization and Function of the Phagophore-ER Membrane Contact Sites
inferred← citeshttps://doi.org/10.1189/jlb.4mr0216-079ropenalex-snapshot
Autophagy in leukocytes and other cells: mechanisms, subsystem organization, selectivity, and links to innate immunity
inferred← citeshttps://doi.org/10.1242/jcs.223792openalex-snapshot
Reconstruction of destruction – in vitro reconstitution methods in autophagy research
inferred← citeshttps://doi.org/10.12688/f1000research.22111.1openalex-snapshot
Recent advances in the understanding of autophagosome biogenesis
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000377openalex-snapshot
Atg11 tethers Atg9 vesicles to initiate selective autophagy
inferred← citeshttps://doi.org/10.14201/gredos.145795openalex-snapshot
Estudio de genes de autofagia y la susceptibilidad a tuberculosis en españoles
inferred← citeshttps://doi.org/10.1515/ntrev-2016-0066openalex-snapshot
Lipid nanotechnologies for structural studies of membrane-associated clotting proteins by cryo-electron microscopy
inferred← citeshttps://doi.org/10.15252/embj.201695189openalex-snapshot
Autophagosome formation is initiated at phosphatidylinositol synthase‐enriched ER subdomains
inferred← citeshttps://doi.org/10.15252/embr.201744559openalex-snapshot
Remodeling of ER‐exit sites initiates a membrane supply pathway for autophagosome biogenesis
inferred← citeshttps://doi.org/10.15252/embr.202050733openalex-snapshot
Function of the SNARE Ykt6 on autophagosomes requires the Dsl1 complex and the Atg1 kinase complex
inferred← citeshttps://doi.org/10.33540/1234openalex-snapshot
Stress granules and Sec bodies: From Drosophila to mammalian cells.
inferred← citeshttps://doi.org/10.3389/fcell.2021.775364openalex-snapshot
Mapping Critical Residues in ATG11’s Coiled-Coil 2 Domain that Block Multiple Interactions and Disrupt Selective Autophagy
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1019543openalex-snapshot
The crucial role of the regulatory mechanism of the Atg1/ULK1 complex in fungi
inferred← citeshttps://doi.org/10.3389/fnsyn.2022.829354openalex-snapshot
Organization of Presynaptic Autophagy-Related Processes
inferred← citeshttps://doi.org/10.3389/fpls.2018.01837openalex-snapshot
The Multivesicular Body and Autophagosome Pathways in Plants
inferred← citeshttps://doi.org/10.3390/antiox11122484openalex-snapshot
Complex Interplay between Autophagy and Oxidative Stress in the Development of Endometriosis
inferred← citeshttps://doi.org/10.3390/biom7030052openalex-snapshot
Regulation of Autophagy through TORC1 and mTORC1
inferred← citeshttps://doi.org/10.3390/cells10113124openalex-snapshot
Activation Mechanisms of the VPS34 Complexes
inferred← citeshttps://doi.org/10.3390/cells11121876openalex-snapshot
Characterization of Protein–Membrane Interactions in Yeast Autophagy
inferred← citeshttps://doi.org/10.3390/cells12081132openalex-snapshot
Membrane Curvature: The Inseparable Companion of Autophagy
inferred← citeshttps://doi.org/10.3390/cells8121627openalex-snapshot
Structural Biology and Electron Microscopy of the Autophagy Molecular Machinery
inferred← citeshttps://doi.org/10.3390/cells8121655openalex-snapshot
Syntaxin 16’s Newly Deciphered Roles in Autophagy
inferred← citeshttps://doi.org/10.3390/ijms20081856openalex-snapshot
Identification and Characterization of Four Autophagy-Related Genes That Are Expressed in Response to Hypoxia in the Brain of the Oriental River Prawn (Macrobrachium nipponense)
inferred← citeshttps://doi.org/10.3390/ijms21218051openalex-snapshot
Recent Advances in Single-Particle Electron Microscopic Analysis of Autophagy Degradation Machinery
inferred← citeshttps://doi.org/10.3390/ijms222212466openalex-snapshot
Over Fifty Years of Life, Death, and Cannibalism: A Historical Recollection of Apoptosis and Autophagy
inferred← citeshttps://doi.org/10.3390/ijms24032221openalex-snapshot
To Kill or to Be Killed: How Does the Battle between the UPS and Autophagy Maintain the Intracellular Homeostasis in Eukaryotes?
inferred← citeshttps://doi.org/10.3390/insects17080862openalex-snapshot
CLCuMuV-Induced Autophagy Restricts Viral Accumulation in the MED Cryptic Species of Bemisia tabaci
inferred← citeshttps://doi.org/10.3390/membranes12050457openalex-snapshot
Theater in the Self-Cleaning Cell: Intrinsically Disordered Proteins or Protein Regions Acting with Membranes in Autophagy
inferred← citeshttps://doi.org/10.3390/membranes16070234openalex-snapshot
A New Anatomy of Autophagic Clearance: On the Roles of Intrinsic Disorder in the Membrane-Less on Membrane-Encapsulated Mechanism
inferred← citeshttps://doi.org/10.3390/plants15091350openalex-snapshot
NBR1-Mediated Selective Autophagy in Plant Development and Stress Responses
inferred← citeshttps://doi.org/10.3410/f.727607153.793572498openalex-snapshot
Faculty Opinions recommendation of Autophagosome formation is initiated at phosphatidylinositol synthase-enriched ER subdomains.
inferred← citeshttps://doi.org/10.3410/f.727849675.793572485openalex-snapshot
Faculty Opinions recommendation of Remodeling of ER-exit sites initiates a membrane supply pathway for autophagosome biogenesis.
inferred← citeshttps://doi.org/10.3410/f.728773296.793572492openalex-snapshot
Faculty Opinions recommendation of Architecture of the ATG2B-WDR45 complex and an aromatic Y/HF motif crucial for complex formation.
inferred← citeshttps://doi.org/10.3410/f.733314698.793572488openalex-snapshot
Faculty Opinions recommendation of Atg9 establishes Atg2-dependent contact sites between the endoplasmic reticulum and phagophores.
inferred← citeshttps://doi.org/10.3410/f.736286434.793564903openalex-snapshot
Faculty Opinions recommendation of Atg11 tethers Atg9 vesicles to initiate selective autophagy.
inferred← citeshttps://doi.org/10.4236/ym.2017.11002openalex-snapshot
Dual Roles of CD38 in Autophagy
inferred← citeshttps://doi.org/10.53846/goediss-6801openalex-snapshot
Dissecting the molecular function of the ubiquitin-like Atg8 during autophagosome biogenesis in S. cerevisiae
inferred← citeshttps://doi.org/10.53846/goediss-7532openalex-snapshot
Atg21 restricts Atg8 lipidation to a novel vacuole-phagophore contact site
inferred← citeshttps://doi.org/10.53846/goediss-7721openalex-snapshot
Dissection of the molecular machinery of micro- and macronucleophagy
inferred← citeshttps://doi.org/10.53846/goediss-8638openalex-snapshot
Identification and Characterization of autophagic and non-autophagic Interaction Partners of Atg18
inferred← citeshttps://doi.org/10.53846/goediss-9145openalex-snapshot
HORMA domain proteins in Autophagy initiation
inferred← citeshttps://doi.org/10.53846/goediss-9302openalex-snapshot
Structure and molecular function of WD-40 repeat-containing autophagy proteins Atg18, Atg21 and Hsv2
inferred← citeshttps://doi.org/10.53846/goediss-9864openalex-snapshot
Biochemical reconstitution of human autophagy initiation
inferred← citeshttps://doi.org/10.5772/intechopen.89683openalex-snapshot
Intracellular Lipid Homeostasis and Trafficking in Autophagy
inferred← citeshttps://doi.org/10.62347/qcpv6064openalex-snapshot
Dual role of autophagy in bone metastasis: mechanistic insights and therapeutic targeting
inferred← citeshttps://doi.org/10.64898/2026.08.17.744853openalex-snapshot
The Z-shaped N-terminal Domain of Atg11 Coordinates Atg9 Binding and Recruitment in Selective Autophagy
inferred← citeshttps://doi.org/10.70675/34dc5979z744bz4dbcz8706z138eacecef37openalex-snapshot
Autophagy in antigen presenting cells
inferred← citeshttps://doi.org/10.70675/4c7f6348zf660z439cz836fz8324fff72f95openalex-snapshot
Une nouvelle mutation du collagène V conduisant, chez le patient, à des atteintes cutanées et musculaires
inferred← citeshttps://doi.org/10.70675/734b2109z0776z4d01za887zfbdb87abb532openalex-snapshot
Unravelling the contribution of lipids in plant autophagy : Identification and functional characterization of lipids implicated in the autophagic process in Arabidopsis
inferred← citeshttps://doi.org/10.7554/elife.29338openalex-snapshot
Atg9 antagonizes TOR signaling to regulate intestinal cell growth and epithelial homeostasis in Drosophila
inferred← citeshttps://doi.org/10.7554/elife.44944openalex-snapshot
COPII vesicles and the expansion of the phagophore
inferred← citeshttps://doi.org/10.7554/elife.59384openalex-snapshot
Toxoplasma TgATG9 is critical for autophagy and long-term persistence in tissue cysts
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