On the public citation graph

Molecular regulation of autophagosome formation

https://doi.org/10.1042/bst20210819

0 signed · 207 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/1873-3468.12901openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.ceb.2019.12.001openalex-snapshot

The ATG conjugation systems in autophagy

inferredcites →https://doi.org/10.1016/j.ceb.2021.02.001openalex-snapshot

Membrane supply and remodeling during autophagosome biogenesis

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/j.cell.2011.06.023openalex-snapshot

Autophagosome Precursor Maturation Requires Homotypic Fusion

inferredcites →https://doi.org/10.1016/j.cell.2013.08.044openalex-snapshot

Diverse Autophagosome Membrane Sources Coalesce in Recycling Endosomes

inferredcites →https://doi.org/10.1016/j.cell.2013.12.022openalex-snapshot

Molecular Mechanism of Autophagic Membrane-Scaffold Assembly and Disassembly

inferredcites →https://doi.org/10.1016/j.cell.2019.12.005openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.cell.2021.10.017openalex-snapshot

Mammalian hybrid pre-autophagosomal structure HyPAS generates autophagosomes

inferredcites →https://doi.org/10.1016/j.celrep.2019.08.069openalex-snapshot

Multilayered Control of Protein Turnover by TORC1 and Atg1

inferredcites →https://doi.org/10.1016/j.cmet.2019.03.003openalex-snapshot

Watch What You (Self-) Eat: Autophagic Mechanisms that Modulate Metabolism

inferredcites →https://doi.org/10.1016/j.cub.2012.06.029openalex-snapshot

Phosphatidylinositol-3-Phosphate Clearance Plays a Key Role in Autophagosome Completion

inferredcites →https://doi.org/10.1016/j.cub.2015.05.042openalex-snapshot

WHAMM Directs the Arp2/3 Complex to the ER for Autophagosome Biogenesis through an Actin Comet Tail Mechanism

inferredcites →https://doi.org/10.1016/j.cub.2017.02.061openalex-snapshot

The Cytoskeleton–Autophagy Connection

inferredcites →https://doi.org/10.1016/j.cub.2018.02.034openalex-snapshot

Coordination of Autophagosome–Lysosome Fusion by Atg8 Family Members

inferredcites →https://doi.org/10.1016/j.cub.2018.03.002openalex-snapshot

The ER Contact Proteins VAPA/B Interact with Multiple Autophagy Proteins to Modulate Autophagosome Biogenesis

inferredcites →https://doi.org/10.1016/j.devcel.2019.01.027openalex-snapshot

Phosphorylation of Syntaxin 17 by TBK1 Controls Autophagy Initiation

inferredcites →https://doi.org/10.1016/j.devcel.2021.07.015openalex-snapshot

Autophagic elimination of ribosomes during spermiogenesis provides energy for flagellar motility

inferredcites →https://doi.org/10.1016/j.febslet.2010.02.013openalex-snapshot

The Cvt pathway as a model for selective autophagy

inferredcites →https://doi.org/10.1016/j.febslet.2015.05.008openalex-snapshot

Function of human WIPI proteins in autophagosomal rejuvenation of endomembranes?

inferredcites →https://doi.org/10.1016/j.isci.2020.101466openalex-snapshot

Modeling Membrane Morphological Change during Autophagosome Formation

inferredcites →https://doi.org/10.1016/j.jmb.2016.02.004openalex-snapshot

Mechanisms of Selective Autophagy

inferredcites →https://doi.org/10.1016/j.jmb.2017.01.002openalex-snapshot

Autophagosome Maturation and Fusion

inferredcites →https://doi.org/10.1016/j.jmb.2019.06.017openalex-snapshot

Mechanistic Insights into the Role of Atg11 in Selective Autophagy

inferredcites →https://doi.org/10.1016/j.molcel.2014.05.021openalex-snapshot

WIPI2 Links LC3 Conjugation with PI3P, Autophagosome Formation, and Pathogen Clearance by Recruiting Atg12–5-16L1

inferredcites →https://doi.org/10.1016/j.molcel.2019.01.035openalex-snapshot

FIP200 Claw Domain Binding to p62 Promotes Autophagosome Formation at Ubiquitin Condensates

inferredcites →https://doi.org/10.1016/j.molcel.2019.01.041openalex-snapshot

The Cargo Receptor NDP52 Initiates Selective Autophagy by Recruiting the ULK Complex to Cytosol-Invading Bacteria

inferredcites →https://doi.org/10.1016/j.molcel.2019.09.005openalex-snapshot

A Diversity of Selective Autophagy Receptors Determines the Specificity of the Autophagy Pathway

inferredcites →https://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

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)00296-xopenalex-snapshot

A Unified Nomenclature for Yeast Autophagy-Related Genes

inferredcites →https://doi.org/10.1038/emboj.2012.225openalex-snapshot

Binding of the Atg1/ULK1 kinase to the ubiquitin‐like protein Atg8 regulates autophagy

inferredcites →https://doi.org/10.1038/emboj.2012.278openalex-snapshot

Mechanism and functions of membrane binding by the Atg5–Atg12/Atg16 complex during autophagosome formation

inferredcites →https://doi.org/10.1038/nature11910openalex-snapshot

Autophagosomes form at ER–mitochondria contact sites

inferredcites →https://doi.org/10.1038/ncb0910-814openalex-snapshot

Eaten alive: a history of macroautophagy

inferredcites →https://doi.org/10.1038/ncb1991openalex-snapshot

A subdomain of the endoplasmic reticulum forms a cradle for autophagosome formation

inferredcites →https://doi.org/10.1038/ncb2078openalex-snapshot

Plasma membrane contributes to the formation of pre-autophagosomal structures

inferredcites →https://doi.org/10.1038/ncb2940openalex-snapshot

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

inferredcites →https://doi.org/10.1038/ncb2979openalex-snapshot

Cargo recognition and trafficking in selective autophagy

inferredcites →https://doi.org/10.1038/ncb3215openalex-snapshot

CapZ regulates autophagosomal membrane shaping by promoting actin assembly inside the isolation membrane

inferredcites →https://doi.org/10.1038/ncomms12420openalex-snapshot

Autophagy initiation by ULK complex assembly on ER tubulovesicular regions marked by ATG9 vesicles

inferredcites →https://doi.org/10.1038/ncomms4920openalex-snapshot

NRBF2 regulates autophagy and prevents liver injury by modulating Atg14L-linked phosphatidylinositol-3 kinase III activity

inferredcites →https://doi.org/10.1038/s41467-017-00302-3openalex-snapshot

Atg4 proteolytic activity can be inhibited by Atg1 phosphorylation

inferredcites →https://doi.org/10.1038/s41467-017-00303-2openalex-snapshot

A reversible phospho-switch mediated by ULK1 regulates the activity of autophagy protease ATG4B

inferredcites →https://doi.org/10.1038/s41467-018-05254-wopenalex-snapshot

An autophagy assay reveals the ESCRT-III component CHMP2A as a regulator of phagophore closure

inferredcites →https://doi.org/10.1038/s41580-020-0241-0openalex-snapshot

Mechanisms governing autophagosome biogenesis

inferredcites →https://doi.org/10.1038/s41580-021-00392-4openalex-snapshot

Machinery, regulation and pathophysiological implications of autophagosome maturation

inferredcites →https://doi.org/10.1038/s41586-020-1977-6openalex-snapshot

Phase separation organizes the site of autophagosome formation

inferredcites →https://doi.org/10.1038/s41586-020-2992-3openalex-snapshot

Wetting regulates autophagy of phase-separated compartments and the cytosol

inferredcites →https://doi.org/10.1038/s41594-019-0203-4openalex-snapshot

Atg2 mediates direct lipid transfer between membranes for autophagosome formation

inferredcites →https://doi.org/10.1038/s41594-020-00518-wopenalex-snapshot

Atg9 is a lipid scramblase that mediates autophagosomal membrane expansion

inferredcites →https://doi.org/10.1038/s41594-020-00520-2openalex-snapshot

Structure, lipid scrambling activity and role in autophagosome formation of ATG9A

inferredcites →https://doi.org/10.1038/s41594-021-00614-5openalex-snapshot

Membrane perturbation by lipidated Atg8 underlies autophagosome biogenesis

inferredcites →https://doi.org/10.1056/nejmra2022774openalex-snapshot

Autophagy in Human Diseases

inferredcites →https://doi.org/10.1073/pnas.1200313109openalex-snapshot

Ume6 transcription factor is part of a signaling cascade that regulates autophagy

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/10.1073/pnas.1806727115openalex-snapshot

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

inferredcites →https://doi.org/10.1074/jbc.c112.387514openalex-snapshot

The Autophagy-related Protein Kinase Atg1 Interacts with the Ubiquitin-like Protein Atg8 via the Atg8 Family Interacting Motif to Facilitate Autophagosome Formation

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.m112.378109openalex-snapshot

ATG8 Family Proteins Act as Scaffolds for Assembly of the ULK Complex

inferredcites →https://doi.org/10.1080/15548627.2019.1639301openalex-snapshot

ESCRT-mediated phagophore sealing during mitophagy

inferredcites →https://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

inferredcites →https://doi.org/10.1080/15548627.2020.1766332openalex-snapshot

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

inferredcites →https://doi.org/10.1080/15548627.2021.1909407openalex-snapshot

Phosphoregulation of the autophagy machinery by kinases and phosphatases

inferredcites →https://doi.org/10.1083/jcb.152.3.519openalex-snapshot

Two Distinct Vps34 Phosphatidylinositol 3–Kinase Complexes Function in Autophagy and Carboxypeptidase Y Sorting in Saccharomyces cerevisiae

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.200803137openalex-snapshot

Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum

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.201111079openalex-snapshot

TBC1D14 regulates autophagosome formation via Rab11- and ULK1-positive recycling endosomes

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.201304123openalex-snapshot

Atg38 is required for autophagy-specific phosphatidylinositol 3-kinase complex integrity

inferredcites →https://doi.org/10.1083/jcb.201607039openalex-snapshot

Atg8 family LC3/GABARAP proteins are crucial for autophagosome–lysosome fusion but not autophagosome formation during PINK1/Parkin mitophagy and starvation

inferredcites →https://doi.org/10.1083/jcb.201710116openalex-snapshot

Atg9 establishes Atg2-dependent contact sites between the endoplasmic reticulum and phagophores

inferredcites →https://doi.org/10.1083/jcb.201804132openalex-snapshot

Genome-wide CRISPR screen identifies TMEM41B as a gene required for autophagosome formation

inferredcites →https://doi.org/10.1083/jcb.201809032openalex-snapshot

COPII vesicles contribute to autophagosomal membranes

inferredcites →https://doi.org/10.1083/jcb.201810099openalex-snapshot

Autophagosome maturation: An epic journey from the ER to lysosomes

inferredcites →https://doi.org/10.1083/jcb.201811139openalex-snapshot

ATG2 transports lipids to promote autophagosome biogenesis

inferredcites →https://doi.org/10.1083/jcb.201811173openalex-snapshot

Rab5-dependent autophagosome closure by ESCRT

inferredcites →https://doi.org/10.1083/jcb.201902170openalex-snapshot

VPS37A directs ESCRT recruitment for phagophore closure

inferredcites →https://doi.org/10.1083/jcb.201909073openalex-snapshot

A conserved myotubularin-related phosphatase regulates autophagy by maintaining autophagic flux

inferredcites →https://doi.org/10.1083/jcb.202103105openalex-snapshot

TMEM41B and VMP1 are scramblases and regulate the distribution of cholesterol and phosphatidylserine

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

Atg8 Controls Phagophore Expansion during Autophagosome Formation

inferredcites →https://doi.org/10.1091/mbc.e08-01-0080openalex-snapshot

Beclin 1 Forms Two Distinct Phosphatidylinositol 3-Kinase Complexes with Mammalian Atg14 and UVRAG

inferredcites →https://doi.org/10.1091/mbc.e08-03-0309openalex-snapshot

The Atg8 Conjugation System Is Indispensable for Proper Development of Autophagic Isolation Membranes in Mice

inferredcites →https://doi.org/10.1091/mbc.e08-03-0312openalex-snapshot

An Atg4B Mutant Hampers the Lipidation of LC3 Paralogues and Causes Defects in Autophagosome Closure

inferredcites →https://doi.org/10.1091/mbc.e11-09-0746openalex-snapshot

Dynamic and transient interactions of Atg9 with autophagosomes, but not membrane integration, are required for autophagy

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/10.1093/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/10.1111/gtc.12733openalex-snapshot

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

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.1365-2443.2009.01299.xopenalex-snapshot

Atg17 recruits Atg9 to organize the pre‐autophagosomal structure

inferredcites →https://doi.org/10.1111/tra.12640openalex-snapshot

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

inferredcites →https://doi.org/10.1126/science.aaf6136openalex-snapshot

The ATG conjugation systems are important for degradation of the inner autophagosomal membrane

inferredcites →https://doi.org/10.1126/science.aaz7714openalex-snapshot

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

inferredcites →https://doi.org/10.1146/annurev-cellbio-120219-035530openalex-snapshot

Mechanisms of Selective Autophagy

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.132415openalex-snapshot

Dynamic association of the ULK1 complex with omegasomes during autophagy induction

inferredcites →https://doi.org/10.1242/jcs.158758openalex-snapshot

ERES: sites for autophagosome biogenesis and maturation?

inferredcites →https://doi.org/10.1242/jcs.235002openalex-snapshot

Vac8 spatially confines autophagosome formation at the vacuole in S. cerevisiae

inferredcites →https://doi.org/10.1371/journal.pone.0032753openalex-snapshot

Curvature of Double-Membrane Organelles Generated by Changes in Membrane Size and Composition

inferredcites →https://doi.org/10.1371/journal.pone.0115357openalex-snapshot

Membrane Morphology Is Actively Transformed by Covalent Binding of the Protein Atg8 to PE-Lipids

inferredcites →https://doi.org/10.15252/embj.201488957openalex-snapshot

PI3P binding by Atg21 organises Atg8 lipidation

inferredcites →https://doi.org/10.15252/embj.201695189openalex-snapshot

Autophagosome formation is initiated at phosphatidylinositol synthase‐enriched ER subdomains

inferredcites →https://doi.org/10.15252/embr.201438618openalex-snapshot

PI3P phosphatase activity is required for autophagosome maturation and autolysosome formation

inferredcites →https://doi.org/10.15252/embr.201744559openalex-snapshot

Remodeling of ER‐exit sites initiates a membrane supply pathway for autophagosome biogenesis

inferredcites →https://doi.org/10.15252/embr.201845889openalex-snapshot

TMEM41B is a novel regulator of autophagy and lipid mobilization

inferredcites →https://doi.org/10.15698/cst2021.09.255openalex-snapshot

Atg8ylation as a general membrane stress and remodeling response

inferredcites →https://doi.org/10.3389/fcell.2016.00020openalex-snapshot

TRAPP Complexes in Secretion and Autophagy

inferredcites →https://doi.org/10.4161/auto.2.2.2298openalex-snapshot

Atg11 Directs Autophagosome Cargoes to the PAS Along Actin Cables

inferredcites →https://doi.org/10.4161/auto.22400openalex-snapshot

It takes two to tango

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.26856openalex-snapshot

Estimating the size and number of autophagic bodies by electron microscopy

inferredcites →https://doi.org/10.4161/auto.5.8.10274openalex-snapshot

3D tomography reveals connections between the phagophore and endoplasmic reticulum

inferredcites →https://doi.org/10.7554/elife.04135openalex-snapshot

Phosphatidylinositol 3-kinase and COPII generate LC3 lipidation vesicles from the ER-Golgi intermediate compartment

What points at this work

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

inferred← citeshttps://doi.org/10.3897/imafungus.17.196033zenodo-depositor-declared

Autophagy as a multi-scale architect of fungal development and pathogenicity: membrane dynamics, multilayer regulation, and cell wall integrity crosstalk

inferred← citeshttps://doi.org/10.1002/1873-3468.14356openalex-snapshot

The complex roles of autophagy in plant immunity

inferred← citeshttps://doi.org/10.1002/1873-3468.14720openalex-snapshot

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

inferred← citeshttps://doi.org/10.1002/cbf.3985openalex-snapshot

The association between ferroptosis and autophagy in cardiovascular diseases

inferred← citeshttps://doi.org/10.1002/cpz1.631openalex-snapshot

Methods to Study Mitochondria: Techniques Used to Study the Effects of Age‐Related Diseases Including Alzheimer's

inferred← citeshttps://doi.org/10.1002/fsn3.70350openalex-snapshot

Food Waste to Wellness: A Grape Pomace Blend in Gastric Cancer Prevention

inferred← citeshttps://doi.org/10.1002/jcb.30416openalex-snapshot

Autophagy‐dependent regulation of MHC‐I molecule presentation

inferred← citeshttps://doi.org/10.1007/978-3-031-88121-3_8openalex-snapshot

Shear Stress-Dependent Regulation of Autophagy and Metabolism in Kidney Epithelial Cells

inferred← citeshttps://doi.org/10.1007/s00018-025-05811-9openalex-snapshot

Ceramide and the membrane-fusion activity of LC3/GABARAP autophagy proteins

inferred← citeshttps://doi.org/10.1007/s00432-024-05910-3openalex-snapshot

ATG10-dependent autophagy is required for DDX10 to regulate cell proliferation, apoptosis and stemness in colorectal cancer

inferred← citeshttps://doi.org/10.1007/s11033-023-08961-wopenalex-snapshot

Revealing the role of epigenetic and post-translational modulations of autophagy proteins in the regulation of autophagy and cancer: a therapeutic approach

inferred← citeshttps://doi.org/10.1007/s11033-026-12474-7openalex-snapshot

Targeting autophagy in oral squamous cell carcinoma chemoresistance: molecular mechanisms, therapeutic strategies, and emerging nanotherapeutic approaches

inferred← citeshttps://doi.org/10.1007/s11101-024-09944-wopenalex-snapshot

Glucosinolates, isothiocyanates, and their role in the regulation of autophagy and cellular function

inferred← citeshttps://doi.org/10.1007/s11655-024-3905-3openalex-snapshot

Tanreqing Injection Inhibits Activation of NLRP3 Inflammasome in Macrophages Infected with Influenza A Virus by Promoting Mitophagy

inferred← citeshttps://doi.org/10.1007/s12032-024-02513-3openalex-snapshot

Regulation of autophagy by non-coding RNAs in human glioblastoma

inferred← citeshttps://doi.org/10.1016/b978-0-323-95672-7.00018-2openalex-snapshot

Autophagy and Huntington's disease

inferred← citeshttps://doi.org/10.1016/j.bbcan.2025.189451openalex-snapshot

Functional dichotomy of autophagy signaling in tumor microenvironment driving hallmarks in oral cancer

inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.151254openalex-snapshot

ATG9 promotes autophagosome formation through interaction with LC3

inferred← citeshttps://doi.org/10.1016/j.cbpb.2026.111267openalex-snapshot

Contrasting effects of short- and long-term starvation on intestinal health and gut microbiome in yellow cheek carp (Elopichthys bambusa)

inferred← citeshttps://doi.org/10.1016/j.ceb.2025.102515openalex-snapshot

Trafficking to the lysosome: HOPS paves the way

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114689openalex-snapshot

The ULK1 effector BAG2 regulates autophagy initiation by modulating AMBRA1 localization

inferred← citeshttps://doi.org/10.1016/j.cophys.2022.100598openalex-snapshot

Glycophagy — the physiological perspective on a newly characterized glycogen-selective autophagy

inferred← citeshttps://doi.org/10.1016/j.devcel.2023.04.015openalex-snapshot

Integrated proteomics identifies p62-dependent selective autophagy of the supramolecular vault complex

inferred← citeshttps://doi.org/10.1016/j.devcel.2024.02.002openalex-snapshot

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

inferred← citeshttps://doi.org/10.1016/j.jneuroim.2025.578716openalex-snapshot

Immunity in Parkinson's disease – The role of innate responses

inferred← citeshttps://doi.org/10.1016/j.ymgme.2026.110130openalex-snapshot

Lysosomal storage, mitochondrial pathology, and autophagy in knockout of tripeptidyl peptidase 1 in human neuroblastoma cells in vitro

inferred← citeshttps://doi.org/10.1017/erm.2023.5openalex-snapshot

Autophagic mechanisms in longevity intervention: role of natural active compounds

inferred← citeshttps://doi.org/10.1021/acsomega.5c06298openalex-snapshot

Research Progress on Regulating Autophagy in Traditional Chinese Medicine for the Treatment of Traumatic Brain Injury

inferred← citeshttps://doi.org/10.1038/s41392-025-02493-4openalex-snapshot

mTOR signaling networks: mechanistic insights and translational frontiers in disease therapeutics

inferred← citeshttps://doi.org/10.1038/s41420-023-01496-wopenalex-snapshot

Autophagy in BRAF-mutant cutaneous melanoma: recent advances and therapeutic perspective

inferred← citeshttps://doi.org/10.1038/s41467-026-77320-7openalex-snapshot

Autophagy inhibition sensitizes radiotherapy responses in high-grade mutant IDH1 glioma

inferred← citeshttps://doi.org/10.1038/s41573-026-01449-9openalex-snapshot

Autophagy modulation in cancer

inferred← citeshttps://doi.org/10.1073/pnas.2211281120openalex-snapshot

The autophagy machinery interacts with EBV capsids during viral envelope release

inferred← citeshttps://doi.org/10.1080/07391102.2024.2425833openalex-snapshot

Molecular dynamics simulations provide insights into ULK-101 potency and selectivity toward autophagic kinases ULK1/2

inferred← citeshttps://doi.org/10.1080/15548627.2023.2269028openalex-snapshot

A conserved requirement for RME-8/DNAJC13 in neuronal autophagic lysosome reformation

inferred← citeshttps://doi.org/10.1080/15548627.2024.2366749openalex-snapshot

An APEX2-based proximity-dependent biotinylation assay with temporal specificity to study protein interactions during autophagy in the yeast Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1080/15548627.2026.2657545openalex-snapshot

SQSTM1/p62-mediated autophagy and antioxidation contribute to white spot syndrome virus pathogenesis in shrimp

inferred← citeshttps://doi.org/10.1080/27694127.2025.2511724openalex-snapshot

A plasmid module for PCR-based gene modification for the accurate measurement of vacuolar delivery of specific proteins in yeast Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1083/jcb.202407014openalex-snapshot

The deubiquitinase USP45 inhibits autophagy through actin regulation by Coronin 1B

inferred← citeshttps://doi.org/10.1091/mbc.e23-08-0328openalex-snapshot

Loss of the HOPS complex disrupts early-to-late endosome transition, impairs endosomal recycling and induces accumulation of amphisomes

inferred← citeshttps://doi.org/10.1091/mbc.e23-12-0470openalex-snapshot

Med13 is required for efficient P-body recruitment and autophagic degradation of Edc3 following nitrogen starvation

inferred← citeshttps://doi.org/10.1097/jd9.0000000000000297openalex-snapshot

Deficiency of Autophagy-Related Gene 5 in Keratinocytes Leads to Aggravation of Epidermal Damage in 2,4-Dinitrochlorobenzene-Induced Allergic Contact Dermatitis

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/10.1101/2023.02.27.530319openalex-snapshot

A Conserved Requirement for RME-8/DNAJC13 in Neuronal Autolysosome Reformation

inferred← citeshttps://doi.org/10.1101/2024.09.22.614367openalex-snapshot

TDRD3 functions as a selective autophagy receptor with dual roles in autophagy and modulation of stress granule stability

inferred← citeshttps://doi.org/10.1101/2025.06.09.658583openalex-snapshot

Balance between autophagy and apoptosis determines anoikis resistance: a mathematical model on cell fate

inferred← citeshttps://doi.org/10.1111/1440-1681.70156openalex-snapshot

18 β‐Glycyrrhetinic Acid Inhibits Malignant Progression of Prostate Cancer via Regulation of Autophagy and EMT Induced by PTEN / PI3K / mTOR Pathway

inferred← citeshttps://doi.org/10.1111/boc.202200073openalex-snapshot

A snapshot of protein trafficking in SARS‐CoV‐2 infection

inferred← citeshttps://doi.org/10.1111/mmi.15034openalex-snapshot

Exploitation of the host exocyst complex by bacterial pathogens

inferred← citeshttps://doi.org/10.1111/tra.12871openalex-snapshot

Developmental program‐independent secretory granule degradation in larval salivary gland cells of Drosophila

inferred← citeshttps://doi.org/10.1128/msphere.00460-23openalex-snapshot

Morphodynamics of non-canonical autophagic structures in Neurospora crassa

inferred← citeshttps://doi.org/10.1155/2023/8408574openalex-snapshot

TRIM72 Alleviates Muscle Inflammation in mdx Mice via Promoting Mitophagy-Mediated NLRP3 Inflammasome Inactivation

inferred← citeshttps://doi.org/10.1177/25152564231217867openalex-snapshot

Canonical and Non-Canonical Roles of SNX1 and SNX2 in Endosomal Membrane Dynamics

inferred← citeshttps://doi.org/10.1186/s10020-025-01299-yopenalex-snapshot

Autophagy in orthodontic tooth movement: advances, challenges, and future perspectives

inferred← citeshttps://doi.org/10.1186/s13578-024-01311-8openalex-snapshot

Golgiphagy: a novel selective autophagy to the fore

inferred← citeshttps://doi.org/10.1186/s43556-026-00430-7openalex-snapshot

Role of autophagy in tumorigenesis and drug resistance: molecular mechanisms and therapeutic targets

inferred← citeshttps://doi.org/10.1242/jcs.264635openalex-snapshot

Vimentin intermediate filaments support autophagosome biogenesis at ER–endosome contact sites in response to starvation

inferred← citeshttps://doi.org/10.12677/acm.2023.13122667openalex-snapshot

Research Progress of Autophagy in Transferrin Receptor Regulation of Gynecologic Tumors

inferred← citeshttps://doi.org/10.1515/hsz-2023-0126openalex-snapshot

Autophagic and non-autophagic functions of the Saccharomyces cerevisiae PROPPINs Atg18, Atg21 and Hsv2

inferred← citeshttps://doi.org/10.21203/rs.3.rs-2271893/v1openalex-snapshot

Transmission Electron Microscopy in the Study of Autophagy: Seeing is Not Always Believing

inferred← citeshttps://doi.org/10.2147/idr.s419646openalex-snapshot

Pseudolaric Acid A: A Promising Antifungal Agent Against Prevalent Non-albicans Candida Species

inferred← citeshttps://doi.org/10.2147/jir.s437067openalex-snapshot

The Potential of Natural Compounds Regulating Autophagy in the Treatment of Osteoporosis

inferred← citeshttps://doi.org/10.3168/jds.2024-25879openalex-snapshot

Cullin 3 mitigates nonesterified fatty acid–induced oxidative stress in mammary epithelial cells: Involvement of BCL2/BECN1 and autophagy

inferred← citeshttps://doi.org/10.3389/fcell.2022.1046248openalex-snapshot

Autophagy and the primary cilium in cell metabolism: What’s upstream?

inferred← citeshttps://doi.org/10.3389/fcvm.2026.1797182openalex-snapshot

Different forms of cardiomyocyte death in post-myocardial infarction ventricular remodeling: mechanisms and therapeutic strategies

inferred← citeshttps://doi.org/10.3389/fimmu.2022.1075804openalex-snapshot

Dual targeting of mTOR/IL-17A and autophagy by fisetin alleviates psoriasis-like skin inflammation

inferred← citeshttps://doi.org/10.3389/fmicb.2024.1411655openalex-snapshot

Herpes Simplex Virus type 1 inhibits autophagy in glial cells but requires ATG5 for the success of viral replication

inferred← citeshttps://doi.org/10.3389/fnagi.2022.1039780openalex-snapshot

The role of microglial autophagy in Parkinson’s disease

inferred← citeshttps://doi.org/10.3389/fphar.2024.1387866openalex-snapshot

Prospects of compounds of herbal plants as anticancer agents: a comprehensive review from molecular pathways

inferred← citeshttps://doi.org/10.3389/fphar.2025.1567552openalex-snapshot

Targeting the programmed cell death signaling mechanism with natural products for the treatment of acute pancreatitis: a review

inferred← citeshttps://doi.org/10.3390/antiox12020428openalex-snapshot

Recent Advances in Cellular Signaling Interplay between Redox Metabolism and Autophagy Modulation in Cancer: An Overview of Molecular Mechanisms and Therapeutic Interventions

inferred← citeshttps://doi.org/10.3390/brainsci13040634openalex-snapshot

Microglia and Astrocytes Dysfunction and Key Neuroinflammation-Based Biomarkers in Parkinson’s Disease

inferred← citeshttps://doi.org/10.3390/cells11193080openalex-snapshot

Morphology of Phagophore Precursors by Correlative Light-Electron Microscopy

inferred← citeshttps://doi.org/10.3390/cells11233813openalex-snapshot

Membrane Contact Sites in Autophagy

inferred← citeshttps://doi.org/10.3390/cells12162056openalex-snapshot

Topology and Function of the S. cerevisiae Autophagy Protein Atg15

inferred← citeshttps://doi.org/10.3390/cells15151340openalex-snapshot

The E. coli High-Pathogenicity Island Downregulates PI3K/Akt/mTOR Expression and Induces Autophagy in the Mouse Intestine

inferred← citeshttps://doi.org/10.3390/cimb46100667openalex-snapshot

Modulation of Autophagy–Lysosome Axis by African Swine Fever Virus and Its Encoded Protein pEP153R

inferred← citeshttps://doi.org/10.3390/ijms23179550openalex-snapshot

Vps21 Directs the PI3K-PI(3)P-Atg21-Atg16 Module to Phagophores via Vps8 for Autophagy

inferred← citeshttps://doi.org/10.3390/ijms232113643openalex-snapshot

Interplay between Autophagy and Herpes Simplex Virus Type 1: ICP34.5, One of the Main Actors

inferred← citeshttps://doi.org/10.3390/ijms241310651openalex-snapshot

The Role of mTORC1 Pathway and Autophagy in Resistance to Platinum-Based Chemotherapeutics

inferred← citeshttps://doi.org/10.3390/ijms241310813openalex-snapshot

Oxytocin Modulates Osteogenic Commitment in Human Adipose-Derived Stem Cells

inferred← citeshttps://doi.org/10.3390/ijms25052918openalex-snapshot

Autophagy and Symbiosis: Membranes, ER, and Speculations

inferred← citeshttps://doi.org/10.3390/ijms27177759openalex-snapshot

Effects of a Chemically Characterised Multi-Component Nutraceutical Formulation on Intestinal, Hepatic and Skeletal Muscle Responses in an In Vitro Gut–Liver–Muscle Model

inferred← citeshttps://doi.org/10.3390/molecules27186101openalex-snapshot

Bioactive Potential: A Pharmacognostic Definition through the Screening of Four Hypericum Species from the Canary Islands

inferred← citeshttps://doi.org/10.3390/ph16020289openalex-snapshot

Cytochalasin B Influences Cytoskeletal Organization and Osteogenic Potential of Human Wharton’s Jelly Mesenchymal Stem Cells

inferred← citeshttps://doi.org/10.3390/plants11212858openalex-snapshot

Identification and Expression Analysis of the Solanum tuberosum StATG8 Family Associated with the WRKY Transcription Factor

inferred← citeshttps://doi.org/10.5937/mp74-44001openalex-snapshot

Volumetric analysis of lymphocyte lipid droplets in type 2 diabetes mellitus patients with hyperlipidemia

inferred← citeshttps://doi.org/10.64898/2025.12.02.691851openalex-snapshot

Vimentin intermediate filaments support autophagosome biogenesis at ER-endosomes contact sites in response to starvation

inferred← citeshttps://doi.org/10.64898/2026.04.29.721097openalex-snapshot

CD4 + T cell activation is dependent on a novel form of ULK1/2-independent autophagy

inferred← citeshttps://doi.org/10.64898/2026.08.27.26360298openalex-snapshot

Loss of RUBCN causes autophagy overdrive in a neurodevelopmental disorder with age-dependent neurodegeneration

inferred← citeshttps://doi.org/10.70675/1dad907cz4477z4068z81c2z087317cd244eopenalex-snapshot

The role of the GATOR1 complex in mitochondrial function and quality control

inferred← citeshttps://doi.org/10.70675/2ddcf286zc553z40fdzb34ez875b3288c76bopenalex-snapshot

Functional characterization of the GATOR1 complex in cisplatin resistance

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.