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ATG9A shapes the forming autophagosome through Arfaptin 2 and phosphatidylinositol 4-kinase IIIβ
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/bbrc.2001.5330openalex-snapshot
Differential Binding of Arfaptin 2/POR1 to ADP-Ribosylation Factors and Rac1
inferredcites →https://doi.org/10.1016/j.cell.2009.04.010openalex-snapshot
The BAR Domain Superfamily: Membrane-Molding Macromolecules
inferredcites →https://doi.org/10.1016/j.cub.2012.10.041openalex-snapshot
The Role of Lipids in the Control of Autophagy
inferredcites →https://doi.org/10.1016/j.devcel.2012.07.019openalex-snapshot
The BAR Domain Protein Arfaptin-1 Controls Secretory Granule Biogenesis at the trans-Golgi Network
inferredcites →https://doi.org/10.1016/j.febslet.2010.01.011openalex-snapshot
Regulation of autophagy by phosphatidylinositol 3‐phosphate
inferredcites →https://doi.org/10.1016/j.jmb.2016.12.013openalex-snapshot
The Journey of the Autophagosome through Mammalian Cell Organelles and Membranes
inferredcites →https://doi.org/10.1016/j.str.2013.12.018openalex-snapshot
Structural Basis for PI(4)P-Specific Membrane Recruitment of the Legionella pneumophila Effector DrrA/SidM
inferredcites →https://doi.org/10.1016/j.tcb.2010.10.002openalex-snapshot
Coordination of Golgi functions by phosphatidylinositol 4-kinases
inferredcites →https://doi.org/10.1016/j.ultramic.2013.10.006openalex-snapshot
Imaging endosomes and autophagosomes in whole mammalian cells using correlative cryo-fluorescence and cryo-soft X-ray microscopy (cryo-CLXM)
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/10.1038/35075620openalex-snapshot
The structural basis of Arfaptin-mediated cross-talk between Rac and Arf signalling pathways
inferredcites →https://doi.org/10.1038/cr.2016.146openalex-snapshot
Regulation of mATG9 trafficking by Src- and ULK1-mediated phosphorylation in basal and starvation-induced autophagy
inferredcites →https://doi.org/10.1038/emboj.2009.321openalex-snapshot
Coordinated regulation of autophagy by p38α MAPK through mAtg9 and p38IP
inferredcites →https://doi.org/10.1038/emboj.2010.338openalex-snapshot
Atg1‐mediated myosin II activation regulates autophagosome formation during starvation‐induced autophagy
inferredcites →https://doi.org/10.1038/emboj.2013.116openalex-snapshot
Recruitment of arfaptins to the trans‐Golgi network by PI(4)P and their involvement in cargo export
inferredcites →https://doi.org/10.1038/ncb1289openalex-snapshot
Protein kinase D regulates vesicular transport by phosphorylating and activating phosphatidylinositol-4 kinase IIIβ at the Golgi complex
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/10.1042/bj20090428openalex-snapshot
Immunocytochemical techniques reveal multiple, distinct cellular pools of PtdIns4 P and PtdIns(4,5) P 2
inferredcites →https://doi.org/10.1042/bj20140889openalex-snapshot
Characterization of VPS34-IN1, a selective inhibitor of Vps34, reveals that the phosphatidylinositol 3-phosphate-binding SGK3 protein kinase is a downstream target of class III phosphoinositide 3-kinase
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.1507263112openalex-snapshot
GABARAPs regulate PI4P-dependent autophagosome:lysosome fusion
inferredcites →https://doi.org/10.1073/pnas.1717327114openalex-snapshot
AP-4 mediates export of ATG9A from the trans -Golgi network to promote autophagosome formation
inferredcites →https://doi.org/10.1074/jbc.272.9.5421openalex-snapshot
Arfaptin 1, a Putative Cytosolic Target Protein of ADP-ribosylation Factor, Is Recruited to Golgi Membranes
inferredcites →https://doi.org/10.1074/jbc.m110.201442openalex-snapshot
Arfaptins Are Localized to the trans-Golgi by Interaction with Arl1, but Not Arfs
inferredcites →https://doi.org/10.1074/jbc.m112.411454openalex-snapshot
Atg9 Vesicles Recruit Vesicle-tethering Proteins Trs85 and Ypt1 to the Autophagosome Formation Site
inferredcites →https://doi.org/10.1074/jbc.m115.673582openalex-snapshot
Protein Kinase D2 Assembles a Multiprotein Complex at the Trans-Golgi Network to Regulate Matrix Metalloproteinase Secretion
inferredcites →https://doi.org/10.1074/jbc.m303221200openalex-snapshot
Interaction Codes within the Family of Mammalian Phox and Bem1p Domain-containing Proteins
inferredcites →https://doi.org/10.1074/jbc.m407528200openalex-snapshot
Phosphorylation of Arfaptin 2 at Ser260 by Akt Inhibits PolyQ-huntingtin-induced Toxicity by Rescuing Proteasome Impairment
inferredcites →https://doi.org/10.1074/jbc.m703663200openalex-snapshot
siRNA Screening of the Kinome Identifies ULK1 as a Multidomain Modulator of Autophagy
inferredcites →https://doi.org/10.1080/15548627.2016.1159378openalex-snapshot
Excess sphingomyelin disturbs ATG9A trafficking and autophagosome closure
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.201312072openalex-snapshot
A novel probe for phosphatidylinositol 4-phosphate reveals multiple pools beyond the Golgi
inferredcites →https://doi.org/10.1083/jcb.201408075openalex-snapshot
Ypt1/Rab1 regulates Hrr25/CK1δ kinase activity in ER–Golgi traffic and macroautophagy
inferredcites →https://doi.org/10.1091/mbc.e08-12-1229openalex-snapshot
The Function of the Intermediate Compartment in Pre-Golgi Trafficking Involves its Stable Connection with the Centrosome
inferredcites →https://doi.org/10.1091/mbc.e10-11-0893openalex-snapshot
The LC3 recruitment mechanism is separate from Atg9L1-dependent membrane formation in the autophagic response againstSalmonella
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/10.1096/fj.201601052ropenalex-snapshot
Small GTPase Rab1B is associated with ATG9A vesicles and regulates autophagosome formation
inferredcites →https://doi.org/10.1126/science.1092586openalex-snapshot
BAR Domains as Sensors of Membrane Curvature: The Amphiphysin BAR Structure
inferredcites →https://doi.org/10.1128/mcb.01082-08openalex-snapshot
Kinase-Inactivated ULK Proteins Inhibit Autophagy via Their Conserved C-Terminal Domains Using an Atg13-Independent Mechanism
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154005openalex-snapshot
The Role of Atg Proteins in Autophagosome Formation
inferredcites →https://doi.org/10.1152/physrev.00028.2012openalex-snapshot
Phosphoinositides: Tiny Lipids With Giant Impact on Cell Regulation
inferredcites →https://doi.org/10.1242/jcs.03172openalex-snapshot
Starvation and ULK1-dependent cycling of mammalian Atg9 between the TGN and endosomes
inferredcites →https://doi.org/10.1242/jcs.093203openalex-snapshot
AP1 is essential for generation of autophagosomes from trans-Golgi network
inferredcites →https://doi.org/10.1242/jcs.114.24.4543openalex-snapshot
Regulation of Golgi structure and function by ARF-like protein 1 (Arl1)
inferredcites →https://doi.org/10.1242/jcs.132415openalex-snapshot
Dynamic association of the ULK1 complex with omegasomes during autophagy induction
inferredcites →https://doi.org/10.1371/journal.pone.0062963openalex-snapshot
Arf1 and Membrane Curvature Cooperate to Recruit Arfaptin2 to Liposomes
inferredcites →https://doi.org/10.15252/embj.201592695openalex-snapshot
TBC1D14 regulates autophagy via the TRAPP complex and ATG9 traffic
inferredcites →https://doi.org/10.15252/embr.201744837openalex-snapshot
SNX18 regulates ATG9A trafficking from recycling endosomes by recruiting Dynamin‐2
inferredcites →https://doi.org/10.18632/oncotarget.8028openalex-snapshot
The Bif-1-Dynamin 2 membrane fission machinery regulates Atg9-containing vesicle generation at the Rab11-positive reservoirs
inferredcites →https://doi.org/10.4161/auto.6.3.11611openalex-snapshot
Regulation of dsDNA-induced innate immune responses by membrane trafficking
inferredcites →https://doi.org/10.4161/auto.6.4.11863openalex-snapshot
Mammalian Atg18 (WIPI2) localizes to omegasome-anchored phagophores and positively regulates LC3 lipidation
inferredcites →https://doi.org/10.4161/auto.7.1.14015openalex-snapshot
Bif-1 regulates Atg9 trafficking by mediating the fission of Golgi membranes during autophagy
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.4009227openalex-extracted
Nondegradable Ubiquitinated ATG9A Organizes Golgi Integrity and Dynamics Upon Stresses
inferred← citeshttps://doi.org/10.1002/1873-3468.13637openalex-snapshot
Hijacking intracellular membranes to feed autophagosomal growth
inferred← citeshttps://doi.org/10.1002/1873-3468.13639openalex-snapshot
Illuminating the membrane contact sites between the endoplasmic reticulum and the trans‐Golgi network
inferred← citeshttps://doi.org/10.1002/1873-3468.14676openalex-snapshot
Membrane association of the ATG8 conjugation machinery emerges as a key regulatory feature for autophagosome biogenesis
inferred← citeshttps://doi.org/10.1002/1873-3468.70213openalex-snapshot
Phosphoinositides in membrane remodeling during infections and cellular stresses
inferred← citeshttps://doi.org/10.1002/ange.202303415openalex-snapshot
Data‐Dependent Acquisition with Precursor Coisolation Improves Proteome Coverage and Measurement Throughput for Label‐Free Single‐Cell Proteomics**
inferred← citeshttps://doi.org/10.1002/anie.202303415openalex-snapshot
Data‐Dependent Acquisition with Precursor Coisolation Improves Proteome Coverage and Measurement Throughput for Label‐Free Single‐Cell Proteomics**
inferred← citeshttps://doi.org/10.1002/bab.2104openalex-snapshot
The interplay of ROS and the PI3K/Akt pathway in autophagy regulation
inferred← citeshttps://doi.org/10.1002/hon.2948openalex-snapshot
Downregulation of FAPP2 gene induces cell autophagy and inhibits PI3K/AKT/mTOR pathway in T‐cell acute lymphoblastic leukemia
inferred← citeshttps://doi.org/10.1007/978-1-0716-2071-7_13openalex-snapshot
Immunofluorescence-Based Measurement of Autophagosome Formation During Mitophagy
inferred← citeshttps://doi.org/10.1007/978-3-031-88121-3_5openalex-snapshot
The Source of Membrane During Autophagy and the Early Steps in Autophagosome Formation
inferred← citeshttps://doi.org/10.1007/s00018-022-04371-6openalex-snapshot
Integrating intracellular nanovesicles into integrin trafficking pathways and beyond
inferred← citeshttps://doi.org/10.1007/s00018-024-05180-9openalex-snapshot
The Janus-faced functions of Apolipoproteins L in membrane dynamics
inferred← citeshttps://doi.org/10.1007/s10549-024-07355-1openalex-snapshot
Combined transcriptome and proteome analysis reveals MSN and ARFIP2 as biomarkers for trastuzumab resistance of breast cancer
inferred← citeshttps://doi.org/10.1007/s12268-024-2295-6openalex-snapshot
Neues zur Struktur und Funktion von ATG9-Vesikeln in Synapsen
inferred← citeshttps://doi.org/10.1007/s13105-026-01243-6openalex-snapshot
Emerging mechanisms of ATG8-independent non-canonical autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-822003-0.00013-9openalex-snapshot
Mechanisms of autophagy: the machinery of macroautophagy and points of control
inferred← citeshttps://doi.org/10.1016/j.ajps.2024.100927openalex-snapshot
Autophagy and mitophagy as potential therapeutic targets in diabetic heart condition: Harnessing the power of nanotheranostics
inferred← citeshttps://doi.org/10.1016/j.antiviral.2025.106100openalex-snapshot
Targeting PI4KB and Src/Abl host kinases as broad-spectrum antiviral strategy: Myth or real opportunity?
inferred← citeshttps://doi.org/10.1016/j.bbalip.2021.158903openalex-snapshot
Phosphoinositides: Functions in autophagy-related stress responses
inferred← citeshttps://doi.org/10.1016/j.bbalip.2022.159184openalex-snapshot
Essential roles of phosphatidylinositol 4-phosphate phosphatases Sac1p and Sjl3p in yeast autophagosome formation
inferred← citeshttps://doi.org/10.1016/j.bbalip.2025.159626openalex-snapshot
Regulation and function of PI4P at the Golgi complex
inferred← citeshttps://doi.org/10.1016/j.bbalip.2025.159673openalex-snapshot
Phosphoinositides as regulators of membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2023.119653openalex-snapshot
Protein kinase D (PKD) on the crossroad of lipid absorption, synthesis and utilization
inferred← citeshttps://doi.org/10.1016/j.bbamem.2021.183731openalex-snapshot
Molecular and mesoscopic geometries in autophagosome generation. A review
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.113967openalex-snapshot
Therapeutic potentials of modulating autophagy in pathological cardiac hypertrophy
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.2026.102651openalex-snapshot
Building the autophagosome: Molecular logic and membrane dynamics of autophagy
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.064openalex-snapshot
APOL1 C-Terminal Variants May Trigger Kidney Disease through Interference with APOL3 Control of Actomyosin
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111195openalex-snapshot
Nondegradable ubiquitinated ATG9A organizes Golgi integrity and dynamics upon stresses
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113528openalex-snapshot
Apolipoproteins L1 and L3 control mitochondrial membrane dynamics
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115993openalex-snapshot
ER-endosome contacts generate a local environment promoting phagophore formation
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.06.054openalex-snapshot
Unraveling membrane properties at the organelle-level with LipidDyn
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.05.007openalex-snapshot
ATG9A and ARFIP2 cooperate to control PI4P levels for lysosomal repair
inferred← citeshttps://doi.org/10.1016/j.drup.2024.101170openalex-snapshot
Autophagy in cancer development, immune evasion, and drug resistance
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174300openalex-snapshot
Research progress of phosphatidylinositol 4-kinase and its inhibitors in inflammatory diseases
inferred← citeshttps://doi.org/10.1016/j.hest.2022.04.003openalex-snapshot
Gene expression changes implicate specific peripheral immune responses to Deep and Lobar Intracerebral Hemorrhages in humans
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107767openalex-snapshot
Iron regulatory protein two facilitates ferritinophagy and DNA damage/repair through guiding ATG9A trafficking
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.111445openalex-snapshot
Golgi-derived phosphatidylinositol 4-phosphate is crucial for organization of the preautophagosomal structure
inferred← citeshttps://doi.org/10.1016/j.jbior.2023.101001openalex-snapshot
A new role for phosphoinositides in regulating mitochondrial dynamics
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.05.051openalex-snapshot
Lipids and Lipid-Binding Proteins in Selective Autophagy
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.09.005openalex-snapshot
Mechanisms of Autophagy in Metabolic Stress Response
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.12.031openalex-snapshot
RAB18 Loss Interferes With Lipid Droplet Catabolism and Provokes Autophagy Network Adaptations
inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168472openalex-snapshot
Physiological functions of ULK1/2
inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168489openalex-snapshot
The Role of ATG9 Vesicles in Autophagosome Biogenesis
inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169138openalex-snapshot
The Role of WIPI2, ATG16L1 and ATG12-ATG5 in Selective and Nonselective Autophagy
inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169288openalex-snapshot
ATG9 Not Just an Autophagy Related Protein
inferred← citeshttps://doi.org/10.1016/j.kint.2020.07.034openalex-snapshot
APOL1 variant–associated kidney disease: from trypanosomes to podocyte cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.livres.2023.02.002openalex-snapshot
Molecular mechanisms of autophagy and implications in liver diseases
inferred← citeshttps://doi.org/10.1016/j.molcel.2019.10.035openalex-snapshot
The ER-Localized Transmembrane Protein TMEM39A/SUSR2 Regulates Autophagy by Controlling the Trafficking of the PtdIns(4)P Phosphatase SAC1
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.molcel.2022.10.017openalex-snapshot
ATG9A and ATG2A form a heteromeric complex essential for autophagosome formation
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.04.021openalex-snapshot
Unconventional initiation of PINK1/Parkin mitophagy by Optineurin
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.04.026openalex-snapshot
Metamorphic proteins at the basis of human autophagy initiation and lipid transfer
inferred← citeshttps://doi.org/10.1016/j.nbd.2021.105595openalex-snapshot
Endophilin-B regulates autophagy during synapse development and neurodegeneration
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.tcb.2020.12.005openalex-snapshot
The Complex Dance of Organelles during Mitochondrial Division
inferred← citeshttps://doi.org/10.1016/j.tcb.2021.04.003openalex-snapshot
ATG4: More Than a Protease?
inferred← citeshttps://doi.org/10.1016/j.tibs.2020.03.010openalex-snapshot
The Golgi as an Assembly Line to the Autophagosome
inferred← citeshttps://doi.org/10.1038/s41392-024-02004-xopenalex-snapshot
Targeted protein degradation: advances in drug discovery and clinical practice
inferred← citeshttps://doi.org/10.1038/s41419-025-08093-yopenalex-snapshot
TM9SF1 drives the lipophagic flux via AMPK-ULK1 signaling to sustain metabolic fitness in HER2-positive breast cancer
inferred← citeshttps://doi.org/10.1038/s41421-020-0161-3openalex-snapshot
Emerging roles of ATG proteins and membrane lipids in autophagosome formation
inferred← citeshttps://doi.org/10.1038/s41421-020-0166-yopenalex-snapshot
Autophagosome biogenesis and human health
inferred← citeshttps://doi.org/10.1038/s41422-025-01085-9openalex-snapshot
Oncogenic RAS induces a distinctive form of non-canonical autophagy mediated by the P38-ULK1-PI4KB axis
inferred← citeshttps://doi.org/10.1038/s41467-020-19840-4openalex-snapshot
Spatial proteomics defines the content of trafficking vesicles captured by golgin tethers
inferred← citeshttps://doi.org/10.1038/s41467-021-26999-xopenalex-snapshot
The autophagy protein ATG9A enables lipid mobilization from lipid droplets
inferred← citeshttps://doi.org/10.1038/s41467-021-27511-1openalex-snapshot
Convergent use of phosphatidic acid for hepatitis C virus and SARS-CoV-2 replication organelle formation
inferred← citeshttps://doi.org/10.1038/s41467-022-32109-2openalex-snapshot
Phosphatidylinositol-4-phosphate controls autophagosome formation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s41467-024-47505-zopenalex-snapshot
A comprehensive genetic map of cytokine responses in Lyme borreliosis
inferred← citeshttps://doi.org/10.1038/s41467-025-65798-6openalex-snapshot
Disruption of the PIKfyve complex unveils an adaptive mechanism to promote lysosomal repair and mitochondrial homeostasis
inferred← citeshttps://doi.org/10.1038/s41467-026-77368-5openalex-snapshot
A lipid transfer-dependent feedback loop activates ATG9A compartments in autophagy initiation
inferred← citeshttps://doi.org/10.1038/s41556-021-00706-wopenalex-snapshot
ATG9A protects the plasma membrane from programmed and incidental permeabilization
inferred← citeshttps://doi.org/10.1038/s41568-025-00810-1openalex-snapshot
Phosphoinositide kinases in cancer: from molecular mechanisms to therapeutic opportunities
inferred← citeshttps://doi.org/10.1038/s41580-020-0241-0openalex-snapshot
Mechanisms governing autophagosome biogenesis
inferred← citeshttps://doi.org/10.1038/s41580-021-00392-4openalex-snapshot
Machinery, regulation and pathophysiological implications of autophagosome maturation
inferred← citeshttps://doi.org/10.1038/s41580-022-00490-xopenalex-snapshot
Phosphoinositides as membrane organizers
inferred← citeshttps://doi.org/10.1038/s41598-020-76227-7openalex-snapshot
Coxsackievirus infection induces a non-canonical autophagy independent of the ULK and PI3K complexes
inferred← citeshttps://doi.org/10.1038/s41598-024-58487-9openalex-snapshot
Dietary restriction reveals sex-specific expression of the mTOR pathway genes in Japanese quails
inferred← citeshttps://doi.org/10.1039/d3cb00232bopenalex-snapshot
ORP9-PH domain-based fluorescent reporters for visualizing phosphatidylinositol 4-phosphate dynamics in living cells
inferred← citeshttps://doi.org/10.1042/bsr20240200openalex-snapshot
Identification of the GABARAP binding determinant in PI4K2A
inferred← citeshttps://doi.org/10.1073/pnas.2004335117openalex-snapshot
Absence of Sac2/INPP5F enhances the phenotype of a Parkinson’s disease mutation of synaptojanin 1
inferred← citeshttps://doi.org/10.1073/pnas.2200085119openalex-snapshot
The intracellular Ca 2+ channel TRPML3 is a PI3P effector that regulates autophagosome biogenesis
inferred← citeshttps://doi.org/10.1073/pnas.2504921122openalex-snapshot
Plant-specific mitochondrial fission machinery connects mitochondrial dynamics and mitophagosome formation for piecemeal mitophagy
inferred← citeshttps://doi.org/10.1080/15548627.2019.1632124openalex-snapshot
ATG9A supplies PtdIns4P to the autophagosome initiation site
inferred← citeshttps://doi.org/10.1080/15548627.2020.1753926openalex-snapshot
On-demand autophagic network adaptations upon limited lipid availability
inferred← citeshttps://doi.org/10.1080/15548627.2020.1796321openalex-snapshot
PtdIns4P restriction by hydrolase SAC1 decides specific fusion of autophagosomes with lysosomes
inferred← citeshttps://doi.org/10.1080/15548627.2020.1820787openalex-snapshot
An inverted CAV1 (caveolin 1) topology defines novel autophagy-dependent exosome secretion from prostate cancer cells
inferred← citeshttps://doi.org/10.1080/15548627.2020.1847461openalex-snapshot
Protein complexes and neighborhoods driving autophagy
inferred← citeshttps://doi.org/10.1080/15548627.2021.1891848openalex-snapshot
Mouse models for hereditary spastic paraplegia uncover a role of PI4K2A in autophagic lysosome reformation
inferred← citeshttps://doi.org/10.1080/15548627.2021.1909407openalex-snapshot
Phosphoregulation of the autophagy machinery by kinases and phosphatases
inferred← citeshttps://doi.org/10.1080/15548627.2022.2111635openalex-snapshot
TMEM164 is a new determinant of autophagy-dependent ferroptosis
inferred← citeshttps://doi.org/10.1080/15548627.2023.2222556openalex-snapshot
PtdIns4P exchange at endoplasmic reticulum-autolysosome contacts is essential for autophagy and neuronal homeostasis
inferred← citeshttps://doi.org/10.1080/15548627.2023.2274204openalex-snapshot
ATG9 resides on a unique population of small vesicles in presynaptic nerve terminals
inferred← citeshttps://doi.org/10.1080/15548627.2023.2275905openalex-snapshot
ATG9B is a tissue-specific homotrimeric lipid scramblase that can compensate for ATG9A
inferred← citeshttps://doi.org/10.1080/15548627.2024.2322493openalex-snapshot
PtdIns4P is required for the autophagosomal recruitment of STX17 (syntaxin 17) to promote lysosomal fusion
inferred← citeshttps://doi.org/10.1080/15548627.2025.2484604openalex-snapshot
RHOD mediates ATG9A trafficking to promote autophagosome formation during autophagy in cancer
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/10.1080/15548627.2026.2617844openalex-snapshot
Disrupted autophagy overactivates TBK1 and results in mitotic defects promoting chromosomal instability
inferred← citeshttps://doi.org/10.1080/15548627.2026.2667375openalex-snapshot
RPS6KA3/RSK2-mediated phosphorylation of DRAM2 promotes lysosomal targeting and autophagic flux in melanoma
inferred← citeshttps://doi.org/10.1080/19768354.2019.1651766openalex-snapshot
Endogenous leptin promotes autophagy in EBSS-induced PFCs
inferred← citeshttps://doi.org/10.1080/27694127.2022.2042054openalex-snapshot
The ATG5 interactome links clathrin-mediated vesicular trafficking with the autophagosome assembly machinery
inferred← citeshttps://doi.org/10.1083/jcb.201904063openalex-snapshot
ATG9 raises the BAR for PI4P in autophagy
inferred← citeshttps://doi.org/10.1083/jcb.202002085openalex-snapshot
Autophagosome biogenesis: From membrane growth to closure
inferred← citeshttps://doi.org/10.1083/jcb.202106014openalex-snapshot
The core autophagy protein ATG9A controls dynamics of cell protrusions and directed migration
inferred← citeshttps://doi.org/10.1083/jcb.202205135openalex-snapshot
ER as master regulator of membrane trafficking and organelle function
inferred← citeshttps://doi.org/10.1083/jcb.202210078openalex-snapshot
Quantitative analysis of autophagy reveals the role of ATG9 and ATG2 in autophagosome formation
inferred← citeshttps://doi.org/10.1083/jcb.202411092openalex-snapshot
The autophagy protein ATG-9 regulates lysosome function and integrity
inferred← citeshttps://doi.org/10.1091/mbc.e24-03-0101openalex-snapshot
Ubiquitin-mediated recruitment of the ATG9A-ATG2 lipid transfer complex drives clearance of phosphorylated p62 aggregates
inferred← citeshttps://doi.org/10.1093/jb/mvaa089openalex-snapshot
Emerging roles of phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate as regulators of multiple steps in autophagy
inferred← citeshttps://doi.org/10.1101/2021.05.10.443480openalex-snapshot
Convergent use of phosphatidic acid for Hepatitis C virus and SARS-CoV-2 replication organelle formation
inferred← citeshttps://doi.org/10.1101/2022.03.28.486054openalex-snapshot
NDR1/2 kinases regulate membrane trafficking, enable efficient autophagy and prevent neurodegeneration
inferred← citeshttps://doi.org/10.1101/2022.08.03.502680openalex-snapshot
Systematic Analysis of Autophagy Identifies Atg9 Vesicles as the Origin of the Phagophore
inferred← citeshttps://doi.org/10.1101/2022.12.21.521536openalex-snapshot
ATG9A regulates dissociation of recycling endosomes from microtubules leading to formation of influenza A virus liquid condensates
inferred← citeshttps://doi.org/10.1101/2023.09.11.557142openalex-snapshot
Syntaxin 17 recruitment to mature autophagosomes is temporally regulated by PI4P accumulation
inferred← citeshttps://doi.org/10.1101/2023.11.28.569058openalex-snapshot
The formation of ubiquitin rich condensates triggers recruitment of the ATG9A lipid transfer complex to initiate basal autophagy
inferred← citeshttps://doi.org/10.1101/2024.07.23.604321openalex-snapshot
ATG9A and ARFIP2 cooperate to regulate PI4P levels for lysosomal repair
inferred← citeshttps://doi.org/10.1101/2024.08.08.604602openalex-snapshot
Biallelic Loss of Molecular Chaperone Molecule AIP Results in a Novel Severe Multisystem Disease Defined by Defective Proteostasis
inferred← citeshttps://doi.org/10.1101/2024.09.12.612637openalex-snapshot
ATG9 vesicles are a subtype of intracellular nanovesicle
inferred← citeshttps://doi.org/10.1101/2025.07.08.663799openalex-snapshot
The Core Subunit NDUFS2 in Mitochondrial Complex I is Critical to Oxygen Sensing in Human Ductus Arteriosus Smooth Muscle Cells
inferred← citeshttps://doi.org/10.1101/2025.09.18.677011openalex-snapshot
Chaperone AIP Couples mTORC1 Activation and Catabolic Metabolism During Neonatal Development
inferred← citeshttps://doi.org/10.1101/241901openalex-snapshot
Dynamin-2 controls phagophore maturation
inferred← citeshttps://doi.org/10.1101/769059openalex-snapshot
The ATG5 Interactome Links Clathrin Vesicular Trafficking With The ATG8 Lipidation Machinery For Autophagosome Assembly
inferred← citeshttps://doi.org/10.1101/841965openalex-snapshot
Determining the content of vesicles captured by golgin tethers using LOPIT-DC
inferred← citeshttps://doi.org/10.1105/tpc.19.00433openalex-snapshot
Remove, Recycle, Degrade: Regulating Plasma Membrane Protein Accumulation
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.15444openalex-snapshot
The function of apolipoproteins L (APOLs): relevance for kidney disease, neurotransmission disorders, cancer and viral infection
inferred← citeshttps://doi.org/10.1111/tra.12841openalex-snapshot
Molecular mechanisms of PI4K regulation and their involvement in viral replication
inferred← citeshttps://doi.org/10.1126/sciadv.adg2997openalex-snapshot
Structural basis for ATG9A recruitment to the ULK1 complex in mitophagy initiation
inferred← citeshttps://doi.org/10.1134/s0006297920100053openalex-snapshot
Replicative Senescence and Expression of Autophagy Genes in Mesenchymal Stromal Cells
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-120219-035530openalex-snapshot
Mechanisms of Selective Autophagy
inferred← citeshttps://doi.org/10.1146/annurev-pathmechdis-031621-025153openalex-snapshot
The Pathogenesis of African Trypanosomiasis
inferred← citeshttps://doi.org/10.1152/ajpcell.00360.2021openalex-snapshot
Mitochondrial quality surveillance: mitophagy in cardiovascular health and disease
inferred← citeshttps://doi.org/10.1172/jci135124openalex-snapshot
Defective lysosome reformation during autophagy causes skeletal muscle disease
inferred← citeshttps://doi.org/10.1177/25152564261451671openalex-snapshot
ER-driven Contact Sites in Autophagosome Biogenesis Sequence
inferred← citeshttps://doi.org/10.1186/s12964-023-01275-1openalex-snapshot
The Golgi stacking protein GRASP55 is targeted by the natural compound prodigiosin
inferred← citeshttps://doi.org/10.1186/s12964-025-02317-6openalex-snapshot
Progress on multifunctional transmembrane protein ATG9A
inferred← citeshttps://doi.org/10.1186/s12977-019-0480-3openalex-snapshot
The autophagy protein ATG9A promotes HIV-1 infectivity
inferred← citeshttps://doi.org/10.1186/s13578-022-00826-2openalex-snapshot
Mechanism of reduced muscle atrophy via ketone body (D)-3-hydroxybutyrate
inferred← citeshttps://doi.org/10.1186/s13578-024-01311-8openalex-snapshot
Golgiphagy: a novel selective autophagy to the fore
inferred← citeshttps://doi.org/10.1242/jcs.228114openalex-snapshot
Autophagy and endocytosis – interconnections and interdependencies
inferred← citeshttps://doi.org/10.1242/jcs.236679openalex-snapshot
Meeting report – Cell dynamics: organelle–cytoskeleton interface
inferred← citeshttps://doi.org/10.1242/jcs.250670openalex-snapshot
The phosphatidylinositol 3-phosphate-binding protein SNX4 controls ATG9A recycling and autophagy
inferred← citeshttps://doi.org/10.1242/jcs.258997openalex-snapshot
A unifying model for the role of the ATG8 system in autophagy
inferred← citeshttps://doi.org/10.1242/jcs.261081openalex-snapshot
Exploring the ATG9A interactome uncovers interaction with VPS13A
inferred← citeshttps://doi.org/10.1242/jcs.263852openalex-snapshot
ATG9A vesicles are a subtype of intracellular nanovesicle
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002290openalex-snapshot
ATG9A regulates the dissociation of recycling endosomes from microtubules to form liquid influenza A virus inclusions
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/10.15252/embj.2020105985openalex-snapshot
Phosphoproteomic identification of ULK substrates reveals VPS15‐dependent ULK/VPS34 interplay in the regulation of autophagy
inferred← citeshttps://doi.org/10.15252/embj.2022112387openalex-snapshot
STING directly recruits WIPI2 for autophagosome formation during STING‐induced autophagy
inferred← citeshttps://doi.org/10.15252/embr.202051136openalex-snapshot
BioID reveals an ATG9A interaction with ATG13-ATG101 in the degradation of p62/SQSTM1-ubiquitin clusters
inferred← citeshttps://doi.org/10.15698/cst2020.07.225openalex-snapshot
The role of lipids in autophagy and its implication in neurodegeneration
inferred← citeshttps://doi.org/10.1681/asn.2020070954openalex-snapshot
The Mechanism of Kidney Disease Due to APOL1 Risk Variants
inferred← citeshttps://doi.org/10.21203/rs.3.rs-147914/v1openalex-snapshot
Glia Maturation Factor-Gamma Regulates Autophagy and Scavenger Receptor-Mediated Phagocytosis in Murine Macrophages
inferred← citeshttps://doi.org/10.2147/jhc.s392056openalex-snapshot
ARFIP2 Regulates EMT and Autophagy in Hepatocellular Carcinoma in Part Through the PI3K/Akt Signalling Pathway
inferred← citeshttps://doi.org/10.26508/lsa.202201652openalex-snapshot
A SNX1–SNX2–VAPB partnership regulates endosomal membrane rewiring in response to nutritional stress
inferred← citeshttps://doi.org/10.26508/lsa.202201712openalex-snapshot
Loss of NDR1/2 kinases impairs endomembrane trafficking and autophagy leading to neurodegeneration
inferred← citeshttps://doi.org/10.3389/fcell.2020.00343openalex-snapshot
Endoplasmic Reticulum Membrane and Contact Site Dynamics in Autophagy Regulation and Stress Response
inferred← citeshttps://doi.org/10.3389/fcell.2021.664788openalex-snapshot
Functions of Oxysterol-Binding Proteins at Membrane Contact Sites and Their Control by Phosphoinositide Metabolism
inferred← citeshttps://doi.org/10.3389/fmolb.2025.1675073openalex-snapshot
Differential roles for CLA-1L and UNC-10 in endosomal maturation and peptide release at C. elegans synapses impacting lifespan
inferred← citeshttps://doi.org/10.3389/fpls.2020.00565openalex-snapshot
Recent Advances in Membrane Shaping for Plant Autophagosome Biogenesis
inferred← citeshttps://doi.org/10.3390/antiox13010081openalex-snapshot
ADP-Ribosylation Factor-Interacting Protein 2 Acts as a Novel Regulator of Mitophagy and Autophagy in Podocytes in Diabetic Nephropathy
inferred← citeshttps://doi.org/10.3390/biology9010007openalex-snapshot
The Role of Autophagy in Pancreatic Cancer—Recent Advances
inferred← citeshttps://doi.org/10.3390/biom13091297openalex-snapshot
Regulation of Phosphoinositide Signaling by Scaffolds at Cytoplasmic Membranes
inferred← citeshttps://doi.org/10.3390/biom16101387openalex-snapshot
Synergistic Activity of APOL3 and GBP1 in Antigen Cross-Presentation: A Model
inferred← citeshttps://doi.org/10.3390/biomedicines9030263openalex-snapshot
Noncoding RNAs Associated with Therapeutic Resistance in Pancreatic Cancer
inferred← citeshttps://doi.org/10.3390/brainsci12020247openalex-snapshot
Specific microRNAs for Modulation of Autophagy in Spinal Cord Injury
inferred← citeshttps://doi.org/10.3390/cells10061272openalex-snapshot
How Lipids Contribute to Autophagosome Biogenesis, a Critical Process in Plant Responses to Stresses
inferred← citeshttps://doi.org/10.3390/cells11050780openalex-snapshot
Maintaining Golgi Homeostasis: A Balancing Act of Two Proteolytic Pathways
inferred← citeshttps://doi.org/10.3390/cells11050871openalex-snapshot
The Interplay between Autophagy and Virus Pathogenesis—The Significance of Autophagy in Viral Hepatitis and Viral Hemorrhagic Fevers
inferred← citeshttps://doi.org/10.3390/cells13201738openalex-snapshot
Apolipoprotein-L1 (APOL1): From Sleeping Sickness to Kidney Disease
inferred← citeshttps://doi.org/10.3390/cells13242115openalex-snapshot
Apolipoprotein-L Functions in Membrane Remodeling
inferred← citeshttps://doi.org/10.3390/cells8121655openalex-snapshot
Syntaxin 16’s Newly Deciphered Roles in Autophagy
inferred← citeshttps://doi.org/10.3390/ijms21051572openalex-snapshot
The Transcriptome of Pig Spermatozoa, and Its Role in Fertility
inferred← citeshttps://doi.org/10.3390/ijms24032221openalex-snapshot
To Kill or to Be Killed: How Does the Battle between the UPS and Autophagy Maintain the Intracellular Homeostasis in Eukaryotes?
inferred← citeshttps://doi.org/10.3390/ijms25073604openalex-snapshot
Galectin-3 and Autophagy in Renal Acute Tubular Necrosis
inferred← citeshttps://doi.org/10.3390/kidneydial4020010openalex-snapshot
The Two Levels of Podocyte Dysfunctions Induced by Apolipoprotein L1 Risk Variants
inferred← citeshttps://doi.org/10.3390/microorganisms12071458openalex-snapshot
Assessing the Presence of Phosphoinositides on Autophagosomal Membrane in Yeast by Live Cell Imaging
inferred← citeshttps://doi.org/10.3390/pathogens13121139openalex-snapshot
Hepatitis C Virus NS5A Activates Mitophagy Through Cargo Receptor and Phagophore Formation
inferred← citeshttps://doi.org/10.3390/plants15091350openalex-snapshot
NBR1-Mediated Selective Autophagy in Plant Development and Stress Responses
inferred← citeshttps://doi.org/10.4103/regenmed.regenmed-d-25-00027openalex-snapshot
Inflammation-linked apolipoprotein-L activities: immunity control, mitochondrial repair, pathogen resistance, and disease induction
inferred← citeshttps://doi.org/10.4239/wjd.v16.i5.102994openalex-snapshot
TERT/FOXO1 signaling promotes islet β-cell dysfunction in type 2 diabetes mellitus by regulating ATG9A-mediated autophagy
inferred← citeshttps://doi.org/10.5772/intechopen.89683openalex-snapshot
Intracellular Lipid Homeostasis and Trafficking in Autophagy
inferred← citeshttps://doi.org/10.6084/m9.figshare.20105521openalex-snapshot
Additional file 1 of Mechanism of reduced muscle atrophy via ketone body (D)-3-hydroxybutyrate
inferred← citeshttps://doi.org/10.6084/m9.figshare.20105524openalex-snapshot
Additional file 2 of Mechanism of reduced muscle atrophy via ketone body (D)-3-hydroxybutyrate
inferred← citeshttps://doi.org/10.6084/m9.figshare.20105527openalex-snapshot
Additional file 3 of Mechanism of reduced muscle atrophy via ketone body (D)-3-hydroxybutyrate
inferred← citeshttps://doi.org/10.6084/m9.figshare.24257484openalex-snapshot
Additional file 1 of The Golgi stacking protein GRASP55 is targeted by the natural compound prodigiosin
inferred← citeshttps://doi.org/10.6084/m9.figshare.24257597openalex-snapshot
Additional file 2 of The Golgi stacking protein GRASP55 is targeted by the natural compound prodigiosin
inferred← citeshttps://doi.org/10.64898/2026.02.03.703515openalex-snapshot
Decoding ATG9A Variation: A Comprehensive Structural Investigation of All Missense Variants
inferred← citeshttps://doi.org/10.70675/36fce390z878bz4402zadafza843c7def083openalex-snapshot
Rôle des protéines LC3/GABARAP dans l'assemblage du VIH-1
inferred← citeshttps://doi.org/10.70675/7104d6d5z945ez494eza917zda9e6be1eea6openalex-snapshot
Interaction entre autophagie et exosomes au niveau synaptique dans la maladie de Parkinson
inferred← citeshttps://doi.org/10.70675/734b2109z0776z4d01za887zfbdb87abb532openalex-snapshot
Unravelling the contribution of lipids in plant autophagy : Identification and functional characterization of lipids implicated in the autophagic process in Arabidopsis
inferred← citeshttps://doi.org/10.70675/92766df5z1811z4470z97f3ze6b8287ff2dbopenalex-snapshot
Analyse des fonctions de la protéine du réticulum endoplasmique, PDZD-8 dans l'autophagie chez Caenorhabditis elegans
inferred← citeshttps://doi.org/10.70962/jhi.20250259openalex-snapshot
Apolipoproteins L involvement in immunity
inferred← citeshttps://doi.org/10.7150/ijbs.83205openalex-snapshot
Molecular Modulators and Receptors of Selective Autophagy: Disease Implication and Identification Strategies
inferred← citeshttps://doi.org/10.7554/elife.58281openalex-snapshot
Membrane characteristics tune activities of endosomal and autophagic human VPS34 complexes
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