On the public citation graph

Dual roles of Atg8−PE deconjugation by Atg4 in autophagy

https://doi.org/10.4161/auto.19652

0 signed · 282 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1097-0061(199807)14:10<953::aid-yea293>3.0.co;2-uopenalex-snapshot

Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae

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.cell.2007.05.021openalex-snapshot

Atg8, a Ubiquitin-like Protein Required for Autophagosome Formation, Mediates Membrane Tethering and Hemifusion

inferredcites →https://doi.org/10.1016/s1534-5807(02)00373-8openalex-snapshot

Mechanism of Cargo Selection in the Cytoplasm to Vacuole Targeting Pathway

inferredcites →https://doi.org/10.1016/s1534-5807(03)00402-7openalex-snapshot

The Atg1-Atg13 Complex Regulates Atg9 and Atg23 Retrieval Transport from the Pre-Autophagosomal Structure

inferredcites →https://doi.org/10.1038/35044114openalex-snapshot

A ubiquitin-like system mediates protein lipidation

inferredcites →https://doi.org/10.1038/emboj.2010.74openalex-snapshot

LC3 and GATE‐16/GABARAP subfamilies are both essential yet act differently in autophagosome biogenesis

inferredcites →https://doi.org/10.1038/nature06421openalex-snapshot

Toll-like receptor signalling in macrophages links the autophagy pathway to phagocytosis

inferredcites →https://doi.org/10.1038/nature06639openalex-snapshot

Autophagy fights disease through cellular self-digestion

inferredcites →https://doi.org/10.1038/nature07961openalex-snapshot

The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins

inferredcites →https://doi.org/10.1038/ncb0910-823openalex-snapshot

Autophagy in mammalian development and differentiation

inferredcites →https://doi.org/10.1038/ncb1007-1102openalex-snapshot

Autophagosome formation: core machinery and adaptations

inferredcites →https://doi.org/10.1038/nrm2708openalex-snapshot

Dynamics and diversity in autophagy mechanisms: lessons from yeast

inferredcites →https://doi.org/10.1038/sj.emboj.7601692openalex-snapshot

Dual mechanisms specify Doa4‐mediated deubiquitination at multivesicular bodies

inferredcites →https://doi.org/10.1074/jbc.275.8.5845openalex-snapshot

The Itinerary of a Vesicle Component, Aut7p/Cvt5p, Terminates in the Yeast Vacuole via the Autophagy/Cvt Pathways

inferredcites →https://doi.org/10.1074/jbc.c700195200openalex-snapshot

The Atg12-Atg5 Conjugate Has a Novel E3-like Activity for Protein Lipidation in Autophagy

inferredcites →https://doi.org/10.1074/jbc.m109.080374openalex-snapshot

Roles of the Lipid-binding Motifs of Atg18 and Atg21 in the Cytoplasm to Vacuole Targeting Pathway and Autophagy

inferredcites →https://doi.org/10.1074/jbc.m109134200openalex-snapshot

Convergence of Multiple Autophagy and Cytoplasm to Vacuole Targeting Components to a Perivacuolar Membrane Compartment Prior tode Novo Vesicle Formation

inferredcites →https://doi.org/10.1074/jbc.m404399200openalex-snapshot

Cargo Proteins Facilitate the Formation of Transport Vesicles in the Cytoplasm to Vacuole Targeting Pathway

inferredcites →https://doi.org/10.1083/jcb.147.2.435openalex-snapshot

Formation Process of Autophagosome Is Traced with Apg8/Aut7p in Yeast

inferredcites →https://doi.org/10.1083/jcb.151.2.263openalex-snapshot

The Reversible Modification Regulates the Membrane-Binding State of Apg8/Aut7 Essential for Autophagy and the Cytoplasm to Vacuole Targeting Pathway

inferredcites →https://doi.org/10.1083/jcb.152.1.51openalex-snapshot

Membrane Recruitment of Aut7p in the Autophagy and Cytoplasm to Vacuole Targeting Pathways Requires Aut1p, Aut2p, and the Autophagy Conjugation Complex

inferredcites →https://doi.org/10.1083/jcb.200507002openalex-snapshot

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

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.e07-12-1257openalex-snapshot

The Atg16L Complex Specifies the Site of LC3 Lipidation for Membrane Biogenesis in Autophagy

inferredcites →https://doi.org/10.1091/mbc.e07-12-1292openalex-snapshot

Atg8 Controls Phagophore Expansion during Autophagosome Formation

inferredcites →https://doi.org/10.1093/emboj/16.8.1820openalex-snapshot

Endosomal transport function in yeast requires a novel AAA‐type ATPase, Vps4p

inferredcites →https://doi.org/10.1093/emboj/19.21.5720openalex-snapshot

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

inferredcites →https://doi.org/10.1093/emboj/20.21.5971openalex-snapshot

The pre‐autophagosomal structure organized by concerted functions of APG genes is essential for autophagosome formation

inferredcites →https://doi.org/10.1093/nar/30.6.e23openalex-snapshot

A second set of loxP marker cassettes for Cre-mediated multiple gene knockouts in budding yeast

inferredcites →https://doi.org/10.1111/j.1600-0854.2007.00553.xopenalex-snapshot

Evidence for a Direct Role of the Doa4 Deubiquitinating Enzyme in Protein Sorting into the MVB Pathway

inferredcites →https://doi.org/10.1128/mcb.8.11.4936openalex-snapshot

Protein sorting in Saccharomyces cerevisiae: isolation of mutants defective in the delivery and processing of multiple vacuolar hydrolases.

inferredcites →https://doi.org/10.1128/mmbr.62.1.230-247.1998openalex-snapshot

Vacuole Biogenesis in Saccharomyces cerevisiae : Protein Transport Pathways to the Yeast Vacuole

inferredcites →https://doi.org/10.1523/jneurosci.0919-07.2007openalex-snapshot

C-Terminal Modification Is Required for GABARAP-Mediated GABAA Receptor Trafficking

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/cbic.202000359openalex-snapshot

Distinct Mechanisms for Processing Autophagy Protein LC3‐PE by RavZ and ATG4B

inferred← citeshttps://doi.org/10.1002/cbic.202500432openalex-snapshot

Artificial Peptides as Autophagy Modulators

inferred← citeshttps://doi.org/10.1002/med.21772openalex-snapshot

The regulatory factors and pathological roles of autophagy‐related protein 4 in diverse diseases: Recent research advances

inferred← citeshttps://doi.org/10.1002/smll.201700996openalex-snapshot

Recent Advances in Nanotechnology for Autophagy Detection

inferred← citeshttps://doi.org/10.1002/yea.3803openalex-snapshot

Yeast phospholipase D, Spo14, is not required for macroautophagy

inferred← citeshttps://doi.org/10.1007/978-1-0716-0868-5_16openalex-snapshot

Assays for Autophagy III: Observing Dynamic Protein Trafficking

inferred← citeshttps://doi.org/10.1007/978-1-4614-6561-4_2openalex-snapshot

The Core Molecular Machinery of Autophagosome Formation

inferred← citeshttps://doi.org/10.1007/978-3-030-26780-3_3openalex-snapshot

Regulation and Function of Autophagy During Ferroptosis

inferred← citeshttps://doi.org/10.1007/978-3-319-15263-9_12openalex-snapshot

Cardiac Cytoarchitecture: How to Maintain a Working Heart—Waste Disposal and Recycling in Cardiomyocytes

inferred← citeshttps://doi.org/10.1007/978-981-10-6913-0_7openalex-snapshot

Self-assembled Nanomaterials for Autophagy Detection and Enhanced Cancer Therapy Through Modulating Autophagy

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_12openalex-snapshot

Biomarkers of Autophagy

inferred← citeshttps://doi.org/10.1007/978-981-16-2830-6_3openalex-snapshot

Phagophore Closure

inferred← citeshttps://doi.org/10.1007/s00018-015-2034-8openalex-snapshot

Autophagy signal transduction by ATG proteins: from hierarchies to networks

inferred← citeshttps://doi.org/10.1007/s00018-017-2657-zopenalex-snapshot

Anatomy of autophagy: from the beginning to the end

inferred← citeshttps://doi.org/10.1007/s00018-022-04281-7openalex-snapshot

Interaction of ToLCNDV TrAP with SlATG8f marks it susceptible to degradation by autophagy

inferred← citeshttps://doi.org/10.1007/s10493-017-0193-zopenalex-snapshot

Relative transcription of autophagy-related genes in Amblyomma sculptum and Rhipicephalus microplus ticks

inferred← citeshttps://doi.org/10.1007/s10549-020-05795-zopenalex-snapshot

Differential expression and prognostic relevance of autophagy-related markers ATG4B, GABARAP, and LC3B in breast cancer

inferred← citeshttps://doi.org/10.1007/s11515-014-1293-3openalex-snapshot

Structural biology of the macroautophagy machinery

inferred← citeshttps://doi.org/10.1007/s12032-018-1220-6openalex-snapshot

The Influence of Tumor Microenvironment on ATG4D Gene Expression in Colorectal Cancer Patients

inferred← citeshttps://doi.org/10.1007/s13238-020-00793-9openalex-snapshot

Lipids and membrane-associated proteins in autophagy

inferred← citeshttps://doi.org/10.1007/s13311-014-0320-zopenalex-snapshot

Promoting Autophagic Clearance: Viable Therapeutic Targets in Alzheimer's Disease

inferred← citeshttps://doi.org/10.1007/s42977-022-00123-6openalex-snapshot

The evolutionary and functional divergence of the Atg8 autophagy protein superfamily

inferred← citeshttps://doi.org/10.1016/b978-0-12-800186-8.00004-3openalex-snapshot

Unselective Disposal of Cellular Aggregates

inferred← citeshttps://doi.org/10.1016/b978-0-12-802937-4.00005-3openalex-snapshot

Is Selective Autophagy Distinct from Starvation-Induced Autophagy?

inferred← citeshttps://doi.org/10.1016/b978-0-12-815868-5.00015-3openalex-snapshot

Nuclear factor erythroid 2-related factor 2 in Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/bs.ircmb.2017.07.001openalex-snapshot

Membrane Trafficking in Autophagy

inferred← citeshttps://doi.org/10.1016/bs.mie.2016.10.024openalex-snapshot

Measurement of the Activity of the Atg4 Cysteine Proteases

inferred← citeshttps://doi.org/10.1016/j.abb.2018.03.001openalex-snapshot

ATG4B inhibitor FMK-9a induces autophagy independent on its enzyme inhibition

inferred← citeshttps://doi.org/10.1016/j.bbagen.2021.129932openalex-snapshot

Yeast mitophagy: Unanswered questions

inferred← citeshttps://doi.org/10.1016/j.bbagrm.2025.195131openalex-snapshot

Autophagy-related genes and encoded proteins' prognostic significance in various cancer types: A molecular perspective

inferred← citeshttps://doi.org/10.1016/j.bbalip.2020.158868openalex-snapshot

Lipid profiles of autophagic structures isolated from wild type and Atg2 mutant Drosophila

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.bbrc.2022.09.065openalex-snapshot

Inhibition of the ATG4-LC3 pathway suppressed osteoclast maturation

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2017.06.042openalex-snapshot

“In vivo self-assembled” nanoprobes for optimizing autophagy-mediated chemotherapy

inferred← citeshttps://doi.org/10.1016/j.canlet.2016.01.022openalex-snapshot

Unraveling the roles of Atg4 proteases from autophagy modulation to targeted cancer therapy

inferred← citeshttps://doi.org/10.1016/j.cellsig.2021.109956openalex-snapshot

PFKP facilitates ATG4B phosphorylation during amino acid deprivation-induced autophagy

inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109899openalex-snapshot

Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation

inferred← citeshttps://doi.org/10.1016/j.cotox.2017.10.006openalex-snapshot

Reciprocity in ROS and autophagic signaling

inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.05.086openalex-snapshot

Identification of benzo[cd]indol-2(1H)-ones as novel Atg4B inhibitors via a structure-based virtual screening and a novel AlphaScreen assay

inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.118686openalex-snapshot

Structure-based discovery of a novel allosteric activator of ATG4B for the treatment of triple-negative breast cancer

inferred← citeshttps://doi.org/10.1016/j.febslet.2014.11.050openalex-snapshot

Storage lipid synthesis is necessary for autophagy induced by nitrogen starvation

inferred← citeshttps://doi.org/10.1016/j.gene.2016.05.036openalex-snapshot

Aberrant methylation of ATG2B , ATG4D , ATG9A and ATG9B CpG island promoter is associated with decreased mRNA expression in sporadic breast carcinoma

inferred← citeshttps://doi.org/10.1016/j.ijpharm.2024.124198openalex-snapshot

Systemic administration of a novel Beclin 1-derived peptide significantly upregulates autophagy in the spinal motor neurons of autophagy reporter mice

inferred← citeshttps://doi.org/10.1016/j.jcmgh.2021.09.017openalex-snapshot

Rab9 Mediates Pancreatic Autophagy Switch From Canonical to Noncanonical, Aggravating Experimental Pancreatitis

inferred← citeshttps://doi.org/10.1016/j.jconrel.2023.02.032openalex-snapshot

MSC-derived extracellular vesicles as nanotherapeutics for promoting aged liver regeneration

inferred← citeshttps://doi.org/10.1016/j.jip.2025.108500openalex-snapshot

Bmced6 enhances BmNPV infection in BmN cells by modulating autophagy and mitochondrial homeostasis

inferred← citeshttps://doi.org/10.1016/j.jmb.2017.01.002openalex-snapshot

Autophagosome Maturation and Fusion

inferred← citeshttps://doi.org/10.1016/j.jmb.2019.10.028openalex-snapshot

Autophagosome-Lysosome Fusion

inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168588openalex-snapshot

Beyond the C-terminal Glycine of ATG8 Proteins – The Story of Some Neglected Amino Acids

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.2025.169235openalex-snapshot

Structural Insights into Autophagy in the AlphaFold Era

inferred← citeshttps://doi.org/10.1016/j.lfs.2019.116642openalex-snapshot

WITHDRAWN: Cinobufagin induced cell apoptosis and protective autophagy through the ROS/MAPK signaling pathway

inferred← citeshttps://doi.org/10.1016/j.micpath.2019.103762openalex-snapshot

Mycophenolic acid (MPA) modulates host cellular autophagy progression in sub genomic dengue virus-2 replicon cells

inferred← citeshttps://doi.org/10.1016/j.molcel.2013.12.014openalex-snapshot

Interactions between Autophagy Receptors and Ubiquitin-like Proteins Form the Molecular Basis for Selective Autophagy

inferred← citeshttps://doi.org/10.1016/j.molcel.2021.03.001openalex-snapshot

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

inferred← citeshttps://doi.org/10.1016/j.neuron.2020.01.018openalex-snapshot

The Journey of the Synaptic Autophagosome: A Cell Biological Perspective

inferred← citeshttps://doi.org/10.1016/j.plipres.2026.101384openalex-snapshot

Nature, functions and trafficking of membrane lipids to support autophagosome formation in plant cells

inferred← citeshttps://doi.org/10.1016/j.redox.2022.102284openalex-snapshot

Suppression of ATG4B by copper inhibits autophagy and involves in Mallory body formation

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.170924openalex-snapshot

Exposure to polystyrene nanoplastics induces apoptosis, autophagy, histopathological damage, and intestinal microbiota dysbiosis of the Pacific whiteleg shrimp (Litopenaeus vannamei)

inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.07.009openalex-snapshot

SNARE-mediated membrane fusion in autophagy

inferred← citeshttps://doi.org/10.1016/j.stress.2025.101200openalex-snapshot

Differential induction of autophagy and miRNA-mediated regulation modulate salt tolerance in contrasting rice varieties

inferred← citeshttps://doi.org/10.1016/j.tibs.2013.06.008openalex-snapshot

Emerging roles of E3 ubiquitin ligases in autophagy

inferred← citeshttps://doi.org/10.1016/j.tice.2025.103240openalex-snapshot

Clinical correlates of key autophagic markers, ATG4B, LC3 and p62 in urothelial carcinoma of bladder patients

inferred← citeshttps://doi.org/10.1016/j.tim.2020.09.012openalex-snapshot

Host Delipidation Mediated by Bacterial Effectors

inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.04.009openalex-snapshot

Autophagy in C. elegans development

inferred← citeshttps://doi.org/10.1016/j.ymeth.2014.12.008openalex-snapshot

The yeast Saccharomyces cerevisiae: An overview of methods to study autophagy progression

inferred← citeshttps://doi.org/10.1021/acsnano.6b07843openalex-snapshot

An in Situ Intracellular Self-Assembly Strategy for Quantitatively and Temporally Monitoring Autophagy

inferred← citeshttps://doi.org/10.1038/cddiscovery.2017.52openalex-snapshot

TRAIL DR5-CTSB crosstalk participates in breast cancer autophagy initiated by SAHA

inferred← citeshttps://doi.org/10.1038/icb.2014.81openalex-snapshot

Autophagy in T‐cell development, activation and differentiation

inferred← citeshttps://doi.org/10.1038/ja.2017.104openalex-snapshot

Autophagy-regulating protease Atg4: structure, function, regulation and inhibition

inferred← citeshttps://doi.org/10.1038/ncb2940openalex-snapshot

Lipidation of the LC3/GABARAP family of autophagy proteins relies on a membrane-curvature-sensing domain in Atg3

inferred← citeshttps://doi.org/10.1038/nrmicro3160openalex-snapshot

Bacteria–autophagy interplay: a battle for survival

inferred← citeshttps://doi.org/10.1038/nsmb.2527openalex-snapshot

Atg12–Atg5 conjugate enhances E2 activity of Atg3 by rearranging its catalytic site

inferred← citeshttps://doi.org/10.1038/nsmb.2787openalex-snapshot

Dynamic regulation of macroautophagy by distinctive ubiquitin-like proteins

inferred← citeshttps://doi.org/10.1038/s41401-025-01619-2openalex-snapshot

Copper pyrithione, a copper complex ATG4B and autophagy inhibitor, exhibits potent anticancer effects

inferred← citeshttps://doi.org/10.1038/s41418-021-00776-1openalex-snapshot

ATG4D is the main ATG8 delipidating enzyme in mammalian cells and protects against cerebellar neurodegeneration

inferred← citeshttps://doi.org/10.1038/s41418-024-01438-8openalex-snapshot

Temporal dissection of the roles of Atg4 and ESCRT in autophagosome formation in yeast

inferred← citeshttps://doi.org/10.1038/s41421-020-0155-1openalex-snapshot

Activation and targeting of ATG8 protein lipidation

inferred← citeshttps://doi.org/10.1038/s41467-017-00302-3openalex-snapshot

Atg4 proteolytic activity can be inhibited by Atg1 phosphorylation

inferred← citeshttps://doi.org/10.1038/s41467-024-55754-1openalex-snapshot

ATG8 delipidation is not universally critical for autophagy in plants

inferred← citeshttps://doi.org/10.1038/s41467-025-65328-4openalex-snapshot

PRDX1 promotes testosterone synthesis and attenuates aging via redox regulation of ATG4B to modulate lipophagy

inferred← citeshttps://doi.org/10.1038/s41580-020-0241-0openalex-snapshot

Mechanisms governing autophagosome biogenesis

inferred← citeshttps://doi.org/10.1038/s41594-025-01678-3openalex-snapshot

Phase separation promotes Atg8 lipidation and vesicle condensation for autophagy progression

inferred← citeshttps://doi.org/10.1038/s41598-018-29900-xopenalex-snapshot

A new quinoline-based chemical probe inhibits the autophagy-related cysteine protease ATG4B

inferred← citeshttps://doi.org/10.1042/bse0550039openalex-snapshot

Two ubiquitin-like conjugation systems that mediate membrane formation during autophagy

inferred← citeshttps://doi.org/10.1042/bse0550051openalex-snapshot

The Atg8 family: multifunctional ubiquitin-like key regulators of autophagy

inferred← citeshttps://doi.org/10.1042/bse0550065openalex-snapshot

Autophagosome maturation and lysosomal fusion

inferred← citeshttps://doi.org/10.1042/bst20170102openalex-snapshot

Evolution of tools and methods for monitoring autophagic flux in mammalian cells

inferred← citeshttps://doi.org/10.1073/pnas.2426476122openalex-snapshot

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

inferred← citeshttps://doi.org/10.1074/jbc.ac119.009977openalex-snapshot

Human ATG4 autophagy proteases counteract attachment of ubiquitin-like LC3/GABARAP proteins to other cellular proteins

inferred← citeshttps://doi.org/10.1074/jbc.m115.658088openalex-snapshot

ATG4B (Autophagin-1) Phosphorylation Modulates Autophagy

inferred← citeshttps://doi.org/10.1074/jbc.ra120.013897openalex-snapshot

The insufficiency of ATG4A in macroautophagy

inferred← citeshttps://doi.org/10.1080/07391102.2020.1869100openalex-snapshot

Virtual screening and repurposing of FDA-approved drugs from ZINC database to identify potential autophagy inhibitors exploiting autophagy related 4A cysteine peptidase as a target: potential as novel anti-cancer molecule.

inferred← citeshttps://doi.org/10.1080/08916934.2024.2351872openalex-snapshot

New insight in treating autoimmune diseases by targeting autophagy

inferred← citeshttps://doi.org/10.1080/09553002.2020.1721597openalex-snapshot

The role of radiation induced oxidative stress as a regulator of radio-adaptive responses

inferred← citeshttps://doi.org/10.1080/15548627.2015.1009773openalex-snapshot

AU4S: A novel synthetic peptide to measure the activity of ATG4 in living cells

inferred← citeshttps://doi.org/10.1080/15548627.2017.1287651openalex-snapshot

ATG4B contains a C-terminal LIR motif important for binding and efficient cleavage of mammalian orthologs of yeast Atg8

inferred← citeshttps://doi.org/10.1080/15548627.2017.1320467openalex-snapshot

Autophagy impairment mediated by S-nitrosation of ATG4B leads to neurotoxicity in response to hyperglycemia

inferred← citeshttps://doi.org/10.1080/15548627.2018.1437341openalex-snapshot

Delipidation of mammalian Atg8-family proteins by each of the four ATG4 proteases

inferred← citeshttps://doi.org/10.1080/15548627.2018.1438807openalex-snapshot

Cholesterol impairs autophagy-mediated clearance of amyloid beta while promoting its secretion

inferred← citeshttps://doi.org/10.1080/15548627.2018.1517073openalex-snapshot

Discovery of a small molecule targeting autophagy via ATG4B inhibition and cell death of colorectal cancer cells in vitro and in vivo

inferred← citeshttps://doi.org/10.1080/15548627.2019.1569925openalex-snapshot

Redundancy of human ATG4 protease isoforms in autophagy and LC3/GABARAP processing revealed in cells

inferred← citeshttps://doi.org/10.1080/15548627.2020.1715047openalex-snapshot

Transgenic expression of GFP-LC3 perturbs autophagy in exocrine pancreas and acute pancreatitis responses in mice

inferred← citeshttps://doi.org/10.1080/15548627.2020.1823124openalex-snapshot

New insights regarding SNARE proteins in autophagosome-lysosome fusion

inferred← citeshttps://doi.org/10.1080/15548627.2021.1943179openalex-snapshot

Activation of microlipophagy during early infection of insect hosts by Metarhizium robertsii

inferred← citeshttps://doi.org/10.1080/15548627.2021.1976965openalex-snapshot

Mechanistic insights into an atypical interaction between ATG8 and SH3P2 in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1080/15548627.2022.2025572openalex-snapshot

Atg8–PE protein-based in vitro biochemical approaches to autophagy studies

inferred← citeshttps://doi.org/10.1080/15548627.2023.2179845openalex-snapshot

The LC3B FRET biosensor monitors the modes of action of ATG4B during autophagy in living cells

inferred← citeshttps://doi.org/10.1080/15548627.2024.2325304openalex-snapshot

Lopinavir enhances anoikis by remodeling autophagy in a circRNA-dependent manner

inferred← citeshttps://doi.org/10.1080/15548627.2024.2369436openalex-snapshot

Last but not least: emerging roles of the autophagy-related protein ATG4D

inferred← citeshttps://doi.org/10.1080/15548627.2025.2471142openalex-snapshot

Cancer-associated mutations in autophagy-related proteins analyzed in yeast and human cells

inferred← citeshttps://doi.org/10.1080/15548627.2025.2531036openalex-snapshot

MoOrp-mediated PtdIns4P transportation is essential for autophagy and pathogenicity in Magnaporthe oryzae

inferred← citeshttps://doi.org/10.1080/21541248.2016.1213090openalex-snapshot

Quo vadis? Interferon-inducible GTPases go to their target membranes via the LC3-conjugation system of autophagy

inferred← citeshttps://doi.org/10.1080/27694127.2023.2188523openalex-snapshot

Atg8 family proteins, LIR/AIM motifs and other interaction modes

inferred← citeshttps://doi.org/10.1093/abbs/gmy032openalex-snapshot

Effects of ovarian hormone loss on neuritic plaques and autophagic flux in the brains of adult female APP/PS1 double-transgenic mice

inferred← citeshttps://doi.org/10.1093/jmcb/mjab059openalex-snapshot

Membrane dynamics of ATG4B and LC3 in autophagosome formation

inferred← citeshttps://doi.org/10.1093/jxb/erab063openalex-snapshot

The ATG4 protease integrates redox and stress signals to regulate autophagy

inferred← citeshttps://doi.org/10.1093/jxb/erx425openalex-snapshot

Modulation of plant autophagy during pathogen attack

inferred← citeshttps://doi.org/10.1093/plphys/kiad520openalex-snapshot

Redox-mediated activation of ATG3 promotes ATG8 lipidation and autophagy progression in Chlamydomonas reinhardtii

inferred← citeshttps://doi.org/10.1094/phyto-01-21-0015-ropenalex-snapshot

The Autophagy-Related Gene CpAtg4 Is Required for Fungal Phenotypic Traits, Stress Tolerance, and Virulence in Cryphonectria parasitica

inferred← citeshttps://doi.org/10.1101/2020.11.18.388306openalex-snapshot

Subtractive CRISPR screen identifies factors involved in non-canonical LC3 lipidation

inferred← citeshttps://doi.org/10.1101/2023.01.24.525316openalex-snapshot

Redox-mediated activation of ATG3 promotes ATG8 lipidation and autophagy progression in Chlamydomonas

inferred← citeshttps://doi.org/10.1101/2024.08.29.610189openalex-snapshot

Phase separation promotes Atg8 lipidation for autophagy progression

inferred← citeshttps://doi.org/10.1101/287144openalex-snapshot

Retrograde Transport and ATG-4.2-Mediated Maturation Cooperate to Remove Autophagosomes from the Synapse

inferred← citeshttps://doi.org/10.1104/pp.16.01582openalex-snapshot

Control of Autophagy in Chlamydomonas Is Mediated through Redox-Dependent Inactivation of the ATG4 Protease

inferred← citeshttps://doi.org/10.1105/tpc.20.00766openalex-snapshot

Abscisic Acid-Triggered Persulfidation of the Cys Protease ATG4 Mediates Regulation of Autophagy by Sulfide

inferred← citeshttps://doi.org/10.1111/cmi.12754openalex-snapshot

LC3-association with the parasitophorous vacuole membrane ofPlasmodium bergheiliver stages follows a noncanonical autophagy pathway

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/10.1111/jcmm.13933openalex-snapshot

Upregulation of AMPK by 4‐O‐methylascochlorin promotes autophagy via the HIF ‐1α expression

inferred← citeshttps://doi.org/10.1111/mpp.70350openalex-snapshot

Functional Dissection of the Turnip Crinkle Virus Coat Protein Links ATG8 Association to Autophagy‐Associated Antiviral Regulation

inferred← citeshttps://doi.org/10.1111/nph.14627openalex-snapshot

Limited and digestive proteolysis: crosstalk between evolutionary conserved pathways

inferred← citeshttps://doi.org/10.1111/tpj.15649openalex-snapshot

Phospholipase Dε interacts with autophagy‐related protein 8 and promotes autophagy in Arabidopsis response to nitrogen deficiency

inferred← citeshttps://doi.org/10.1111/tra.12024openalex-snapshot

Trs130 Participates in Autophagy Through GTPases Ypt31/32 in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1128/mcb.00389-20openalex-snapshot

Canonical and Noncanonical Autophagy Pathways in Microglia

inferred← citeshttps://doi.org/10.1134/s0006297916040052openalex-snapshot

Molecular mechanisms of autophagy in plants: Role of ATG8 proteins in formation and functioning of autophagosomes

inferred← citeshttps://doi.org/10.1146/annurev-biochem-060815-014556openalex-snapshot

Mammalian Autophagy: How Does It Work?

inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100818-125242openalex-snapshot

Autophagy in Neurons

inferred← citeshttps://doi.org/10.1152/ajpgi.00053.2023openalex-snapshot

Ethanol inhibits pancreatic acinar cell autophagy through upregulation of ATG4B, mediating pathological responses of alcoholic pancreatitis

inferred← citeshttps://doi.org/10.1155/2015/398483openalex-snapshot

Cellular and Molecular Connections between Autophagy and Inflammation

inferred← citeshttps://doi.org/10.1155/2019/3809308openalex-snapshot

Recent Insights into the Mitochondrial Role in Autophagy and Its Regulation by Oxidative Stress

inferred← citeshttps://doi.org/10.1159/000485286openalex-snapshot

Ablation of ATG4B Suppressed Autophagy and Activated AMPK for Cell Cycle Arrest in Cancer Cells

inferred← citeshttps://doi.org/10.1159/000495274openalex-snapshot

Sulforaphane-N-Acetyl-Cysteine Induces Autophagy Through Activation of ERK1/2 in U87MG and U373MG Cells

inferred← citeshttps://doi.org/10.11648/j.ejb.20140205.11openalex-snapshot

Selective Mitophagy in Budding Yeast, a Mitochondrial Self-Eating Quality Control

inferred← citeshttps://doi.org/10.1172/jci73940openalex-snapshot

The functional and pathologic relevance of autophagy proteases

inferred← citeshttps://doi.org/10.1177/25152564231162495openalex-snapshot

How Membrane Contact Sites Shape the Phagophore

inferred← citeshttps://doi.org/10.1182/bloodadvances.2021005910openalex-snapshot

ATG4A regulates human erythroid maturation and mitochondrial clearance

inferred← citeshttps://doi.org/10.1186/bcr3576openalex-snapshot

A mammosphere formation RNAi screen reveals that ATG4A promotes a breast cancer stem-like phenotype

inferred← citeshttps://doi.org/10.1186/s12915-021-01048-7openalex-snapshot

Membrane recruitment of Atg8 by Hfl1 facilitates turnover of vacuolar membrane proteins in yeast cells approaching stationary phase

inferred← citeshttps://doi.org/10.1186/s12943-024-02172-yopenalex-snapshot

Mechanisms and cross-talk of regulated cell death and their epigenetic modifications in tumor progression

inferred← citeshttps://doi.org/10.1186/s12951-024-02875-wopenalex-snapshot

Nanomaterial-mediated host directed therapy of tuberculosis by manipulating macrophage autophagy

inferred← citeshttps://doi.org/10.1186/s13578-020-00464-6openalex-snapshot

Autophagy in the control and pathogenesis of parasitic infections

inferred← citeshttps://doi.org/10.1186/s13578-020-00467-3openalex-snapshot

Autophagy and its role in regeneration and remodeling within invertebrate

inferred← citeshttps://doi.org/10.1242/jcs.223792openalex-snapshot

Reconstruction of destruction – in vitro reconstitution methods in autophagy research

inferred← citeshttps://doi.org/10.1242/jcs.259725openalex-snapshot

Post-translational modifications of ATG8 proteins – an emerging mechanism of autophagy control

inferred← citeshttps://doi.org/10.12677/acm.2019.93027openalex-snapshot

Advances in the Regulation of Autophagy

inferred← citeshttps://doi.org/10.1360/ssv-2024-0039openalex-snapshot

Strategies for precise regulation of autophagy by traditional Chinese medicine and natural products and their application in neurodegenerative disease models

inferred← citeshttps://doi.org/10.1360/ssv-2026-0054openalex-snapshot

The membrane localization mechanisms and functions of ATG8 family proteins in autophagic and non-autophagic pathways

inferred← citeshttps://doi.org/10.1371/journal.pgen.1005704openalex-snapshot

Retromer Is Essential for Autophagy-Dependent Plant Infection by the Rice Blast Fungus

inferred← citeshttps://doi.org/10.1371/journal.pone.0096059openalex-snapshot

Distribution, Cleavage and Lipidation of Atg8 Fusion Proteins in Spodoptera litura Sl-HP Cells

inferred← citeshttps://doi.org/10.1371/journal.pone.0181047openalex-snapshot

Atg4 plays an important role in efficient expansion of autophagic isolation membranes by cleaving lipidated Atg8 in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1371/journal.pone.0230981openalex-snapshot

Biological functions of the autophagy-related proteins Atg4 and Atg8 in Cryptococcus neoformans

inferred← citeshttps://doi.org/10.1371/journal.ppat.1011988openalex-snapshot

Autophagy and cell wall integrity pathways coordinately regulate the development and pathogenicity through MoAtg4 phosphorylation in Magnaporthe oryzae

inferred← citeshttps://doi.org/10.14232/phd.12136openalex-snapshot

Lipids of autophagic membranes and their role in the recruitment of Syntaxin 17 to the autophagosomes

inferred← citeshttps://doi.org/10.1515/hsz-2025-0187openalex-snapshot

Getting to the right place at the right time – membrane trafficking and maturation in the endolysosomal system

inferred← citeshttps://doi.org/10.15252/embj.201591440openalex-snapshot

Phospholipid methylation controls Atg32‐mediated mitophagy and Atg8 recycling

inferred← citeshttps://doi.org/10.15252/embr.201643146openalex-snapshot

Conserved Atg8 recognition sites mediate Atg4 association with autophagosomal membranes and Atg8 deconjugation

inferred← citeshttps://doi.org/10.15252/embr.201948317openalex-snapshot

TBK1‐mediated phosphorylation of LC3C and GABARAP‐L2 controls autophagosome shedding by ATG4 protease

inferred← citeshttps://doi.org/10.18240/ijo.2018.04.05openalex-snapshot

Autophagy activation and the mechanism of retinal microvascular endothelial cells in hypoxia

inferred← citeshttps://doi.org/10.18632/oncotarget.11408openalex-snapshot

Identification of breast cancer cell subtypes sensitive to ATG4B inhibition

inferred← citeshttps://doi.org/10.18632/oncotarget.22714openalex-snapshot

Atg4 in autophagosome biogenesis

inferred← citeshttps://doi.org/10.18632/oncotarget.9827openalex-snapshot

ATG4A promotes tumor metastasis by inducing the epithelial-mesenchymal transition and stem-like properties in gastric cells

inferred← citeshttps://doi.org/10.21248/gups.67332openalex-snapshot

Minimized combinatorial CRISPR screens identify genetic interactions in autophagy

inferred← citeshttps://doi.org/10.2147/rrbc.s57405openalex-snapshot

The autophagosome: current understanding of formation and maturation

inferred← citeshttps://doi.org/10.26686/wgtn.17067545openalex-snapshot

Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine

inferred← citeshttps://doi.org/10.26686/wgtn.17067545.v1openalex-snapshot

Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine

inferred← citeshttps://doi.org/10.32604/biocell.2021.014844openalex-snapshot

KRT4 suppresses oral squamous cell carcinoma development by reducing ATG4B-mediated autophagy

inferred← citeshttps://doi.org/10.3389/fcell.2020.00466openalex-snapshot

Multiple Functions of ATG8 Family Proteins in Plant Autophagy

inferred← citeshttps://doi.org/10.3389/fcell.2022.799392openalex-snapshot

The Role of Non-Coding RNAs in Autophagy During Carcinogenesis

inferred← citeshttps://doi.org/10.3389/fcell.2025.1532050openalex-snapshot

Mechanisms and roles of membrane-anchored ATG8s

inferred← citeshttps://doi.org/10.3389/fcell.2026.1910706openalex-snapshot

Regulated cell death in ovarian cancer: molecular mechanisms and therapeutic targets

inferred← citeshttps://doi.org/10.3389/fchem.2020.00233openalex-snapshot

Chemical Biology of Autophagy-Related Proteins With Posttranslational Modifications: From Chemical Synthesis to Biological Applications

inferred← citeshttps://doi.org/10.3389/fcimb.2020.599762openalex-snapshot

Interfering with Autophagy: The Opposing Strategies Deployed by Legionella pneumophila and Coxiella burnetii Effector Proteins

inferred← citeshttps://doi.org/10.3389/fimmu.2017.00165openalex-snapshot

Autophagy and Autophagy-Related Proteins in CNS Autoimmunity

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1165507openalex-snapshot

Mitophagy in atherosclerosis: from mechanism to therapy

inferred← citeshttps://doi.org/10.3389/fnagi.2019.00049openalex-snapshot

Influence of Normal Aging on Brain Autophagy: A Complex Scenario

inferred← citeshttps://doi.org/10.3389/fpls.2017.01459openalex-snapshot

Autophagy Is Rapidly Induced by Salt Stress and Is Required for Salt Tolerance in Arabidopsis

inferred← citeshttps://doi.org/10.3389/fpls.2022.866367openalex-snapshot

Monitoring Autophagy in Rice With GFP-ATG8 Marker Lines

inferred← citeshttps://doi.org/10.3390/antiox10121884openalex-snapshot

Autophagy Is Involved in the Viability of Overexpressing Thioredoxin o1 Tobacco BY-2 Cells under Oxidative Conditions

inferred← citeshttps://doi.org/10.3390/biomedicines10061459openalex-snapshot

Therapeutic Aspects and Molecular Targets of Autophagy to Control Pancreatic Cancer Management

inferred← citeshttps://doi.org/10.3390/brainsci12020247openalex-snapshot

Specific microRNAs for Modulation of Autophagy in Spinal Cord Injury

inferred← citeshttps://doi.org/10.3390/cancers11050649openalex-snapshot

Targeting ATG4 in Cancer Therapy

inferred← citeshttps://doi.org/10.3390/cancers11101599openalex-snapshot

Targeting Autophagy for Cancer Treatment and Tumor Chemosensitization

inferred← citeshttps://doi.org/10.3390/cancers12061523openalex-snapshot

New Anti-Cancer Strategy to Suppress Colorectal Cancer Growth Through Inhibition of ATG4B and Lysosome Function

inferred← citeshttps://doi.org/10.3390/cells10113071openalex-snapshot

Atg5 Regulates Selective Autophagy of the Parental Macronucleus during Tetrahymena Sexual Reproduction

inferred← citeshttps://doi.org/10.3390/cells11030507openalex-snapshot

Impact of Organelle Transport Deficits on Mitophagy and Autophagy in Niemann–Pick Disease Type C

inferred← citeshttps://doi.org/10.3390/cells12060899openalex-snapshot

Cytoskeleton Protein BmACT1 Is Potential for the Autophagic Function and Nuclear Localization of BmAtg4b in Bombyx mori

inferred← citeshttps://doi.org/10.3390/cells14161261openalex-snapshot

Disrupted Myelination in FAHN: Insights from a Patient-Specific hiPSC Neuron–Oligodendrocyte Model

inferred← citeshttps://doi.org/10.3390/cells7050037openalex-snapshot

Autophagy in Age-Associated Neurodegeneration

showing the first 200 of 248 · page through all 248

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.