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The Atg2-Atg18 complex tethers pre-autophagosomal membranes to the endoplasmic reticulum for autophagosome formation

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1873-3468.12901openalex-snapshot

Differential requirement for ATG2A domains for localization to autophagic membranes and lipid droplets

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/j.febslet.2006.07.041openalex-snapshot

The relevance of the phosphatidylinositolphosphat‐binding motif FRRGT of Atg18 and Atg21 for the Cvt pathway and autophagy

inferredcites →https://doi.org/10.1038/emboj.2008.248openalex-snapshot

VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P2 in yeast and mouse

inferredcites →https://doi.org/10.1038/nrm3696openalex-snapshot

The autophagosome: origins unknown, biogenesis complex

inferredcites →https://doi.org/10.1038/nsmb1194openalex-snapshot

A general amphipathic α-helical motif for sensing membrane curvature

inferredcites →https://doi.org/10.1038/sj.emboj.7600203openalex-snapshot

Svp1p defines a family of phosphatidylinositol 3,5‐bisphosphate effectors

inferredcites →https://doi.org/10.1073/pnas.1811874115openalex-snapshot

Insights into autophagosome biogenesis from structural and biochemical analyses of the ATG2A-WIPI4 complex

inferredcites →https://doi.org/10.1074/jbc.m102342200openalex-snapshot

Apg2 Is a Novel Protein Required for the Cytoplasm to Vacuole Targeting, Autophagy, and Pexophagy Pathways

inferredcites →https://doi.org/10.1074/jbc.m102346200openalex-snapshot

Apg2p Functions in Autophagosome Formation on the Perivacuolar Structure

inferredcites →https://doi.org/10.1074/jbc.m112.397570openalex-snapshot

Structure-based Analyses Reveal Distinct Binding Sites for Atg2 and Phosphoinositides in Atg18

inferredcites →https://doi.org/10.1074/jbc.m803180200openalex-snapshot

The Atg18-Atg2 Complex Is Recruited to Autophagic Membranes via Phosphatidylinositol 3-Phosphate and Exerts an Essential Function

inferredcites →https://doi.org/10.1080/15548627.2017.1359381openalex-snapshot

Architecture of the ATG2B-WDR45 complex and an aromatic Y/HF motif crucial for complex formation

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/10.1083/jcb.201502105openalex-snapshot

ER–mitochondrial junctions can be bypassed by dominant mutations in the endosomal protein Vps13

inferredcites →https://doi.org/10.1091/mbc.e04-02-0147openalex-snapshot

Atg21 Is a Phosphoinositide Binding Protein Required for Efficient Lipidation and Localization of Atg8 during Uptake of Aminopeptidase I by Selective Autophagy

inferredcites →https://doi.org/10.1091/mbc.e07-04-0301openalex-snapshot

Atg18 Regulates Organelle Morphology and Fab1 Kinase Activity Independent of Its Membrane Recruitment by Phosphatidylinositol 3,5-Bisphosphate

inferredcites →https://doi.org/10.1091/mbc.e13-07-0381openalex-snapshot

ER exit sites are physical and functional core autophagosome biogenesis components

inferredcites →https://doi.org/10.1091/mbc.e16-02-0112openalex-snapshot

Yeast Vps13 promotes mitochondrial function and is localized at membrane contact sites

inferredcites →https://doi.org/10.1093/bioinformatics/16.4.404openalex-snapshot

The PSIPRED protein structure prediction server

inferredcites →https://doi.org/10.1093/jb/mvt025openalex-snapshot

Identification of a second amphipathic lipid-packing sensor-like motif that contributes to Gcs1p function in the early endosome-to-TGN pathway

inferredcites →https://doi.org/10.1101/gad.1998611openalex-snapshot

Phosphoinositide [PI(3,5)P2] lipid-dependent regulation of the general transcriptional regulator Tup1

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/10.1146/annurev-cellbio-092910-154005openalex-snapshot

The Role of Atg Proteins in Autophagosome Formation

inferredcites →https://doi.org/10.1242/jcs.115725openalex-snapshot

Atg18 function in autophagy is regulated by specific sites within its β-propeller

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/10.1242/jcs.158758openalex-snapshot

ERES: sites for autophagosome biogenesis and maturation?

inferredcites →https://doi.org/10.15252/embj.201796697openalex-snapshot

Molecular definitions of autophagy and related processes

inferredcites →https://doi.org/10.15252/embj.201796859openalex-snapshot

Membrane scission driven by the PROPPIN Atg18

inferredcites →https://doi.org/10.4161/auto.6.6.12348openalex-snapshot

Quantification of nonselective bulk autophagy inS. cerevisiaeusing Pgk1-GFP

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Intricacies of Lipid Supply in Autophagic Membrane Expansion

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Phagophore closure, autophagosome maturation and autophagosome fusion during macroautophagy in the yeast Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1002/1873-3468.14726openalex-snapshot

Novel insights into autophagosome biogenesis revealed by cryo‐electron tomography

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Structural view on autophagosome formation

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ATG and ESCRT control multiple modes of microautophagy

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Human WIPI β‐propeller function in autophagy and neurodegeneration

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Omegasomes control formation, expansion, and closure of autophagosomes

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Role of N ‐glycosylation as a determinant of ATG9A conformations and activity

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Birth, Growth, Maturation, and Demise of Plant Autophagic Vesicles

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Autophagy and Huntington's disease

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ER platforms mediating autophagosome generation

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Atg2 and Atg9: Intermembrane and interleaflet lipid transporters driving autophagy

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Cell death as a result of calcium signaling modulation: A cancer-centric prospective

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Small but mighty: Atg8s and Rabs in membrane dynamics during autophagy

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Coordinated regulation of phosphatidylinositol 4-phosphate and phosphatidylserine levels by Osh4p and Osh5p is an essential regulatory mechanism in autophagy

inferred← citeshttps://doi.org/10.1016/j.ceb.2020.02.008openalex-snapshot

Inter-organelle lipid transfer: a channel model for Vps13 and chorein-N motif proteins

inferred← citeshttps://doi.org/10.1016/j.ceb.2020.02.012openalex-snapshot

Autophagosomes are formed at a distinct cellular structure

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.ceb.2025.102493openalex-snapshot

Advances in mitophagy initiation mechanisms

inferred← citeshttps://doi.org/10.1016/j.ceb.2026.102651openalex-snapshot

Building the autophagosome: Molecular logic and membrane dynamics of autophagy

inferred← citeshttps://doi.org/10.1016/j.cell.2019.12.005openalex-snapshot

Local Fatty Acid Channeling into Phospholipid Synthesis Drives Phagophore Expansion during Autophagy

inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107837openalex-snapshot

Structure of Human ATG9A, the Only Transmembrane Protein of the Core Autophagy Machinery

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113599openalex-snapshot

Pib2 is a cysteine sensor involved in TORC1 activation in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2018.11.001openalex-snapshot

Membrane-binding domains in autophagy

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β-propeller proteins WDR45 and WDR45B regulate autophagosome maturation into autolysosomes in neural cells

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Tricalbins Contribute to Cellular Lipid Flux and Form Curved ER-PM Contacts that Are Bridged by Rod-Shaped Structures

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Autophagic elimination of ribosomes during spermiogenesis provides energy for flagellar motility

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An Arabidopsis Rab18 GTPase promotes autophagy by tethering ATG18a to the ER in response to nutrient starvation

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Rim aperture of yeast autophagic membranes balances cargo inclusion with vesicle maturation

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Biomolecular condensates of ATG18 reshape ER for autophagy in plants

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Structural Conservation of the Two Phosphoinositide-Binding Sites in WIPI Proteins

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Phospholipid Supply for Autophagosome Biogenesis

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The PKA Signaling Pathway Regulates the Association of the Autophagy Initiation Complex With the Lipidation Machinery

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ATG4 family proteins drive phagophore growth independently of the LC3/GABARAP lipidation system

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Multilayered regulation of autophagy by the Atg1 kinase orchestrates spatial and temporal control of autophagosome formation

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ATG9A and ATG2A form a heteromeric complex essential for autophagosome formation

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Unconventional initiation of PINK1/Parkin mitophagy by Optineurin

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Metamorphic proteins at the basis of human autophagy initiation and lipid transfer

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MicroRNA-378 contributes to osteoarthritis by regulating chondrocyte autophagy and bone marrow mesenchymal stem cell chondrogenesis

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A novel superfamily of bridge-like lipid transfer proteins

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Emerging roles of ATG proteins and membrane lipids in autophagosome formation

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ANKFY1 bridges ATG2A-mediated lipid transfer from endosomes to phagophores

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Multi-site-mediated entwining of the linear WIR-motif around WIPI β-propellers for autophagy

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Super-assembly of ER-phagy receptor Atg40 induces local ER remodeling at contacts with forming autophagosomal membranes

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Phosphatidylinositol-4-phosphate controls autophagosome formation in Arabidopsis thaliana

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Pexophagy suppresses ROS-induced damage in leaf cells under high-intensity light

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A conserved membrane curvature-generating protein is crucial for autophagosome formation in fission yeast

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Local membrane source gathering by p62 body drives autophagosome formation

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Atg18 oligomer organization in assembled tubes and on lipid membrane scaffolds

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Mechanisms governing autophagosome biogenesis

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Atg2 mediates direct lipid transfer between membranes for autophagosome formation

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Atg9 is a lipid scramblase that mediates autophagosomal membrane expansion

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Structural basis for lipid transfer by the ATG2A–ATG9A complex

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Establishment of the phagophore–ERES membrane contact site initiates phagophore elongation

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Core principles of autophagy initiation mechanisms

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Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth

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Receptor-mediated cargo hitchhiking on bulk autophagy

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S-palmitoylation modulates ATG2-dependent non-vesicular lipid transport during starvation-induced autophagy

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Atg18 interaction positions Atg2 for efficient lipid transfer into phagophore elongation

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Atg23 prevents aberrant fusion of Atg9 vesicles during delivery to autophagosome formation sites

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In vitro reconstitution of autophagic processes

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Molecular regulation of autophagosome formation

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Biogenesis of omegasomes and autophagosomes in mammalian autophagy

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Vps13 is required for the packaging of the ER into autophagosomes during ER-phagy

inferred← citeshttps://doi.org/10.1073/pnas.2023604118openalex-snapshot

Persulfidation of ATG18a regulates autophagy under ER stress in Arabidopsis

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In situ structural analysis reveals membrane shape transitions during autophagosome formation

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In situ snapshots along a mammalian selective autophagy pathway

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The autophagy-specific exocyst subcomplex contributes to phagophore assembly site integrity by promoting phagophore expansion

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The molecular mechanism of lipid uptake by membrane-anchored bridge-like lipid transfer proteins

inferred← citeshttps://doi.org/10.1073/pnas.2606606123openalex-snapshot

Spatiotemporal control of Atg2 association with the ER during autophagosome formation

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Pex3 confines pexophagy receptor activity of Atg36 to peroxisomes by regulating Hrr25-mediated phosphorylation and proteasomal degradation

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Autophagy and stress tolerance in plants: the central role of ATG18—a review

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Molecular dynamics simulations reveal how the reticulon-homology domain of the autophagy receptor RETREG1/FAM134B remodels membranes for efficient selective reticulophagy

inferred← citeshttps://doi.org/10.1080/15548627.2020.1725403openalex-snapshot

The proppin Bcas3 and its interactor KinkyA localize to the early phagophore and regulate autophagy

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As (and when) you like it: on-demand phospholipid synthesis drives phagophore expansion during autophagy

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Atg21 organizes Atg8 lipidation at the contact of the vacuole with the phagophore

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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1

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Autophagy under construction: insights from in vitro reconstitution of autophagosome nucleation

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SHISA5/SCOTIN restrains spontaneous autophagy induction by blocking contact between the ERES and phagophores

inferred← citeshttps://doi.org/10.1080/15548627.2022.2085496openalex-snapshot

Pathogen-induced autophagy regulates monolignol transport and lignin formation in plant immunity

inferred← citeshttps://doi.org/10.1080/15548627.2022.2136340openalex-snapshot

Atg9 interactions via its transmembrane domains are required for phagophore expansion during autophagy

inferred← citeshttps://doi.org/10.1080/15548627.2023.2214029openalex-snapshot

Hva22, a REEP family protein in fission yeast, promotes reticulophagy in collaboration with a receptor protein

inferred← citeshttps://doi.org/10.1080/15548627.2023.2259708openalex-snapshot

Ksp1 is an autophagic receptor protein for the Snx4-assisted autophagy of Ssn2/Med13

inferred← citeshttps://doi.org/10.1080/15548627.2024.2330033openalex-snapshot

Quantitative analysis of the spatial distance between autophagy-related membrane structures and the endoplasmic reticulum in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1080/15548627.2024.2394302openalex-snapshot

Myotubularin 2 interacts with SEC23A and negatively regulates autophagy at ER exit sites in Arabidopsis

inferred← citeshttps://doi.org/10.1080/15548627.2024.2440843openalex-snapshot

Endogenous interactomes of MFN1 and MFN2 provide novel insights into interorganelle communication and autophagy

inferred← citeshttps://doi.org/10.1080/15548627.2025.2479427openalex-snapshot

ATG2A acts as a tether to regulate autophagosome-lysosome fusion in neural cells

inferred← citeshttps://doi.org/10.1080/15548627.2026.2671338openalex-snapshot

The autophagic and non-autophagic functions of the S. cerevisiae PROPPIN Hsv2

inferred← citeshttps://doi.org/10.1080/15548627.2026.2671342openalex-snapshot

Formation and function of a novel Atg21-retromer complex in S. cerevisiae

inferred← citeshttps://doi.org/10.1080/21505594.2021.1909954openalex-snapshot

Calcineurin-mediated intracellular organelle calcium homeostasis is required for the survival of fungal pathogens upon extracellular calcium stimuli

inferred← citeshttps://doi.org/10.1080/21505594.2024.2322183openalex-snapshot

Autophagy-related protein PlATG2 regulates the vegetative growth, sporangial cleavage, autophagosome formation, and pathogenicity of peronophythora litchii

inferred← citeshttps://doi.org/10.1083/jcb.201810099openalex-snapshot

Autophagosome maturation: An epic journey from the ER to lysosomes

inferred← citeshttps://doi.org/10.1083/jcb.201811139openalex-snapshot

ATG2 transports lipids to promote autophagosome biogenesis

inferred← citeshttps://doi.org/10.1083/jcb.201903127openalex-snapshot

ERdj8 governs the size of autophagosomes during the formation process

inferred← citeshttps://doi.org/10.1083/jcb.201904159openalex-snapshot

Who plays the ferryman: ATG2 channels lipids into the forming autophagosome

inferred← citeshttps://doi.org/10.1083/jcb.201910063openalex-snapshot

TORC1 inactivation stimulates autophagy of nucleoporin and nuclear pore complexes

inferred← citeshttps://doi.org/10.1083/jcb.202001161openalex-snapshot

Cryo-EM reconstruction of a VPS13 fragment reveals a long groove to channel lipids between membranes

inferred← citeshttps://doi.org/10.1083/jcb.202002085openalex-snapshot

Autophagosome biogenesis: From membrane growth to closure

inferred← citeshttps://doi.org/10.1083/jcb.202009194openalex-snapshot

Transmembrane phospholipid translocation mediated by Atg9 is involved in autophagosome formation

inferred← citeshttps://doi.org/10.1083/jcb.202203045openalex-snapshot

Convergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes

inferred← citeshttps://doi.org/10.1083/jcb.202208088openalex-snapshot

ATG9 vesicles comprise the seed membrane of mammalian autophagosomes

inferred← citeshttps://doi.org/10.1083/jcb.202211039openalex-snapshot

Parallel phospholipid transfer by Vps13 and Atg2 determines autophagosome biogenesis dynamics

inferred← citeshttps://doi.org/10.1083/jcb.202307094openalex-snapshot

A role for Vps13-mediated lipid transfer at the ER–endosome contact site in ESCRT-mediated sorting

inferred← citeshttps://doi.org/10.1083/jcb.202309057openalex-snapshot

Faa1 membrane binding drives positive feedback in autophagosome biogenesis via fatty acid activation

inferred← citeshttps://doi.org/10.1083/jcb.202502131openalex-snapshot

Hoi1 targets BLTP2 to ER–PM contact sites to regulate lipid homeostasis

inferred← citeshttps://doi.org/10.1083/jcb.202601047openalex-snapshot

MOSPD3 mediates the ER recruitment of ATG2A to promote autophagy

inferred← citeshttps://doi.org/10.1091/mbc.e19-08-0477openalex-snapshot

Sec16 function in ER export and autophagy is independent of its phosphorylation inSaccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1091/mbc.e20-03-0191openalex-snapshot

Elevating PI3P drives select downstream membrane trafficking pathways

inferred← citeshttps://doi.org/10.1091/mbc.e24-05-0236openalex-snapshot

Proviral role of ATG2 autophagy related protein in tomato bushy stunt virus replication through bulk phospholipid transfer into the viral replication organelle

inferred← citeshttps://doi.org/10.1091/mbc.e25-06-0273openalex-snapshot

The Atg2-Atg18 complex interacts with the Atg1 complex to localize to the pre-autophagosomal structure in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1093/genetics/iyaf007openalex-snapshot

Conserved components of the macroautophagy machinery in Caenorhabditis elegans

inferred← citeshttps://doi.org/10.1093/hmg/ddab225openalex-snapshot

A conserved ATG2 binding site in WIPI4 and yeast Hsv2 is disrupted by mutations causing β-propeller protein-associated neurodegeneration

inferred← citeshttps://doi.org/10.1093/hmg/ddad096openalex-snapshot

Comprehensive analysis of autophagic functions of WIPI family proteins and their implications for the pathogenesis of β-propeller associated neurodegeneration

inferred← citeshttps://doi.org/10.1093/hmg/ddz318openalex-snapshot

A VPS13D spastic ataxia mutation disrupts the conserved adaptor-binding site in yeast Vps13

inferred← citeshttps://doi.org/10.1093/jb/mvad099openalex-snapshot

Molecular Mechanism of Autophagy, Cytoplasmic Zoning by Lipid Membranes

inferred← citeshttps://doi.org/10.1093/plcell/koab263openalex-snapshot

FYVE2, a phosphatidylinositol 3-phosphate effector, interacts with the COPII machinery to control autophagosome formation in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plcell/koad252openalex-snapshot

HOOKLESS1 acetylates AUTOPHAGY-RELATED PROTEIN18a to promote autophagy during nutrient starvation in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plphys/kiad287openalex-snapshot

Arabidopsis AUTOPHAGY-RELATED2 is essential for ATG18a and ATG9 trafficking during autophagosome closure

inferred← citeshttps://doi.org/10.1096/fj.202301479ropenalex-snapshot

Loss of mitogen‐activated protein kinase phosphate‐5 aggravates islet dysfunction in mice with type 1 and type 2 diabetes

inferred← citeshttps://doi.org/10.1098/rsob.230192openalex-snapshot

Coiled-coil-mediated dimerization of Atg16 is required for binding to the PROPPIN Atg21

inferred← citeshttps://doi.org/10.1098/rsob.240412openalex-snapshot

Autophagy: a novel target in order to overcome drug resistance in pancreatic adenocarcinoma

inferred← citeshttps://doi.org/10.1101/2020.08.23.263939openalex-snapshot

When and why an essential popular mineral—calcium—is an effective antifungal adjuvant against the human pathogen?

inferred← citeshttps://doi.org/10.1101/2022.07.26.501514openalex-snapshot

Structural plasticity of Atg18 oligomers: organization of assembled tubes and scaffolds at the isolation membrane

inferred← citeshttps://doi.org/10.1101/2022.08.03.502596openalex-snapshot

α-Arrestins maintain phospholipid balance and Atg18 distribution to permit efficient autophagy

inferred← citeshttps://doi.org/10.1101/2022.10.27.514035openalex-snapshot

Membrane curvature-generating proteins crucial for autophagosome formation

inferred← citeshttps://doi.org/10.1101/2024.09.09.611943openalex-snapshot

Presynapses are mitophagy pit stops that prevent axon degeneration

inferred← citeshttps://doi.org/10.1101/2024.12.19.629339openalex-snapshot

Phosphatidylinositol-3,5-bisphosphate mediated vacuolar morphology modulation is integral to ethanol stress response

inferred← citeshttps://doi.org/10.1101/2025.01.17.633517openalex-snapshot

Role of N -glycosylation as a determinant of ATG9A conformations and activity

inferred← citeshttps://doi.org/10.1101/2025.02.11.637747openalex-snapshot

Hoi1 targets the yeast BLTP2 protein to ER-PM contact sites to regulate lipid homeostasis

inferred← citeshttps://doi.org/10.1101/2025.03.24.645038openalex-snapshot

ATG2A interacts with RAB1A and ARFGAP1 positive membranes during autophagosome biogenesis

inferred← citeshttps://doi.org/10.1101/2025.11.16.688672openalex-snapshot

Pathway and gates for ATG2A-mediated lipid transport in autophagy

inferred← citeshttps://doi.org/10.1101/624627openalex-snapshot

A conserved ATG2-GABARAP interaction is critical for phagophore closure

inferred← citeshttps://doi.org/10.1101/cshperspect.a041257openalex-snapshot

Endoplasmic Reticulum Membrane Contact Sites, Lipid Transport, and Neurodegeneration

inferred← citeshttps://doi.org/10.1111/1750-3841.71385openalex-snapshot

Molecular Omics Unveils the Antimicrobial Mechanism of UV‐LED‐Induced Chitosan Composite Film Against Penicillium italicum

inferred← citeshttps://doi.org/10.1111/febs.15127openalex-snapshot

Phosphoinositides in autophagy: current roles and future insights

inferred← citeshttps://doi.org/10.1111/febs.15334openalex-snapshot

Membrane targeting of core autophagy players during autophagosome biogenesis

inferred← citeshttps://doi.org/10.1111/febs.17288openalex-snapshot

Atg2 controls Drosophila hematopoiesis through the PVR / TOR signaling pathways

inferred← citeshttps://doi.org/10.1111/febs.70257openalex-snapshot

Atg18 facilitates autophagosome formation via its Atg8‐interacting motif in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1111/gtc.12733openalex-snapshot

Human ATG2B possesses a lipid transfer activity which is accelerated by negatively charged lipids and WIPI4

inferred← citeshttps://doi.org/10.1111/imb.12869openalex-snapshot

Ame‐miR ‐980‐3p participates in autophagy‐mediated midgut remodelling in Apis mellifera via targeting Atg2B

inferred← citeshttps://doi.org/10.1111/jcmm.14732openalex-snapshot

Manganese activates autophagy to alleviate endoplasmic reticulum stress–induced apoptosis via PERK pathway

inferred← citeshttps://doi.org/10.1111/mmi.14441openalex-snapshot

Autophagy‐related protein Pf ATG18 participates in food vacuole dynamics and autophagy‐like pathway in Plasmodium falciparum

inferred← citeshttps://doi.org/10.1111/mmi.15360openalex-snapshot

The Plasmodium GRASP Homolog Modulates Liver Stage Development, Subsequent Blood Infection and Virulence in Mice

inferred← citeshttps://doi.org/10.1111/nph.19934openalex-snapshot

Rare variations within the serine/arginine‐rich splicing factor PtoRSZ21 modulate stomatal size to determine drought tolerance in Populus

inferred← citeshttps://doi.org/10.1111/nph.20393openalex-snapshot

Blocking constitutive autophagy rescues the loss of acquired heat resistance in Arabidopsis fes1a

inferred← citeshttps://doi.org/10.1111/tra.12640openalex-snapshot

TRAPPC11 functions in autophagy by recruiting ATG2B‐WIPI4/WDR45 to preautophagosomal membranes

inferred← citeshttps://doi.org/10.1126/science.aaz7714openalex-snapshot

Reconstitution of autophagosome nucleation defines Atg9 vesicles as seeds for membrane formation

inferred← citeshttps://doi.org/10.1128/msphere.00771-20openalex-snapshot

Precise Expression of Afmed15 Is Crucial for Asexual Development, Virulence, and Survival of Aspergillus fumigatus

inferred← citeshttps://doi.org/10.1128/msphere.00829-24openalex-snapshot

Toxoplasma gondii PROP1 is critical for autophagy and parasite viability during chronic infection

inferred← citeshttps://doi.org/10.1146/annurev-biochem-083024-122821openalex-snapshot

Lipid Dynamics at Membrane Contact Sites

inferred← citeshttps://doi.org/10.1146/annurev-cellbio-120420-014634openalex-snapshot

RBG Motif Bridge-Like Lipid Transport Proteins: Structure, Functions, and Open Questions

inferred← citeshttps://doi.org/10.1146/annurev-genet-022422-095608openalex-snapshot

The Genetics of Autophagy in Multicellular Organisms

inferred← citeshttps://doi.org/10.1146/annurev-virology-010220-054709openalex-snapshot

Autophagy in Plant-Virus Interactions

inferred← citeshttps://doi.org/10.1152/ajpcell.00360.2021openalex-snapshot

Mitochondrial quality surveillance: mitophagy in cardiovascular health and disease

inferred← citeshttps://doi.org/10.1155/2023/8257217openalex-snapshot

Autophagy and Its Lineage-Specific Roles in the Hematopoietic System

inferred← citeshttps://doi.org/10.1177/2515256418819936openalex-snapshot

The Rod-Shaped ATG2A-WIPI4 Complex Tethers Membranes In Vitro

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