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The yeast autophagy protease Atg4 is regulated by thioredoxin

https://doi.org/10.4161/auto.34396
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What this work says

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

inferredcites →https://doi.org/10.1007/s11120-006-9099-zopenalex-snapshot
Thioredoxin-dependent regulation of photosynthetic glyceraldehyde-3-phosphate dehydrogenase: autonomous vs. CP12-dependent mechanisms
inferredcites →https://doi.org/10.1016/0003-2697(69)90064-5openalex-snapshot
Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: Applications to mammalian blood and other tissues
inferredcites →https://doi.org/10.1016/j.bbamcr.2013.03.019openalex-snapshot
Substrate recognition in selective autophagy and the ubiquitin–proteasome system
inferredcites →https://doi.org/10.1016/j.tibs.2010.07.007openalex-snapshot
Regulation of autophagy by ROS: physiology and pathology
inferredcites →https://doi.org/10.1016/s0021-9258(18)31570-9openalex-snapshot
Thioredoxin deficiency in yeast prolongs S phase and shortens the G1 interval of the cell cycle
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/10.1021/bi982876copenalex-snapshot
Structural Basis for Light Activation of a Chloroplast Enzyme: The Structure of Sorghum NADP-Malate Dehydrogenase in Its Oxidized Form,
inferredcites →https://doi.org/10.1038/35044114openalex-snapshot
A ubiquitin-like system mediates protein lipidation
inferredcites →https://doi.org/10.1038/emboj.2009.80openalex-snapshot
The structure of Atg4B–LC3 complex reveals the mechanism of LC3 processing and delipidation during autophagy
inferredcites →https://doi.org/10.1038/nsmb.2527openalex-snapshot
Atg12–Atg5 conjugate enhances E2 activity of Atg3 by rearranging its catalytic site
inferredcites →https://doi.org/10.1038/sj.emboj.7601623openalex-snapshot
Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.02795.xopenalex-snapshot
Role of thioredoxins in the response of Saccharomyces cerevisiae to oxidative stress induced by hydroperoxides
inferredcites →https://doi.org/10.1073/pnas.0611636104openalex-snapshot
Molecular mechanism of thioredoxin regulation in photosynthetic A 2 B 2 -glyceraldehyde-3-phosphate dehydrogenase
inferredcites →https://doi.org/10.1073/pnas.1318207111openalex-snapshot
Differential processing of Arabidopsis ubiquitin-like Atg8 autophagy proteins by Atg4 cysteine proteases
inferredcites →https://doi.org/10.1074/jbc.273.7.3963openalex-snapshot
Tor, a Phosphatidylinositol Kinase Homologue, Controls Autophagy in Yeast
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.m509158200openalex-snapshot
Structural Basis for the Specificity and Catalysis of Human Atg4B Responsible for Mammalian Autophagy
inferredcites →https://doi.org/10.1074/jbc.m709567200openalex-snapshot
Biochemical Characterization of Glutaredoxins from Chlamydomonas reinhardtii Reveals the Unique Properties of a Chloroplastic CGFS-type Glutaredoxin
inferredcites →https://doi.org/10.1074/mcp.m111.014035openalex-snapshot
Identification of Autophagosome-associated Proteins and Regulators by Quantitative Proteomic Analysis and Genetic Screens
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/10.1089/ars.2007.9.25openalex-snapshot
Thioredoxin and Related Molecules–From Biology to Health and Disease
inferredcites →https://doi.org/10.1089/ars.2010.3554openalex-snapshot
Autophagy Signaling Through Reactive Oxygen Species
inferredcites →https://doi.org/10.1089/ars.2012.5033openalex-snapshot
Functions and Cellular Compartmentation of the Thioredoxin and Glutathione Pathways in Yeast
inferredcites →https://doi.org/10.1089/ars.2014.5837openalex-snapshot
Oxidative Stress, Redox Signaling, and Autophagy: Cell Death Versus Survival
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/hmg/ddn178openalex-snapshot
Glutathione-dependent redox status of frataxin-deficient cells in a yeast model of Friedreich's ataxia
inferredcites →https://doi.org/10.1099/00221287-143-6-1885openalex-snapshot
An important role for glutathione and γ-glutamyltranspeptidase in the supply of growth requirements during nitrogen starvation of the yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1101/pdb.top79openalex-snapshot
Stabilization of Proteins for Storage
inferredcites →https://doi.org/10.1104/pp.104.052670openalex-snapshot
NADP-Malate Dehydrogenase from Unicellular Green Alga Chlamydomonas reinhardtii. A First Step toward Redox Regulation?
inferredcites →https://doi.org/10.1104/pp.106.092106openalex-snapshot
Degradation of Oxidized Proteins by Autophagy during Oxidative Stress in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.152520openalex-snapshot
Inhibition of Target of Rapamycin Signaling and Stress Activate Autophagy in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1104/pp.112.199992openalex-snapshot
Reactive Oxygen Species and Autophagy in Plants and Algae
inferredcites →https://doi.org/10.1146/annurev-biochem-052709-094552openalex-snapshot
Biogenesis and Cargo Selectivity of Autophagosomes
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154005openalex-snapshot
The Role of Atg Proteins in Autophagosome Formation
inferredcites →https://doi.org/10.1146/annurev-genet-102808-114910openalex-snapshot
Regulation Mechanisms and Signaling Pathways of Autophagy
inferredcites →https://doi.org/10.1159/000350326openalex-snapshot
Antimicrobial Autophagy: A Conserved Innate Immune Response in Drosophila
inferredcites →https://doi.org/10.3389/fpls.2013.00470openalex-snapshot
Redox regulation of the Calvin–Benson cycle: something old, something new
inferredcites →https://doi.org/10.4161/auto.18864openalex-snapshot
Carotenoid deficiency triggers autophagy in the model green algaChlamydomonas reinhardtii
inferredcites →https://doi.org/10.4161/auto.19385openalex-snapshot
A role for Atg8–PE deconjugation in autophagosome biogenesis
inferredcites →https://doi.org/10.4161/auto.19652openalex-snapshot
Dual roles of Atg8−PE deconjugation by Atg4 in autophagy
inferredcites →https://doi.org/10.4161/auto.6.7.12754openalex-snapshot
Under the ROS: Thiol network is the principal suspect for autophagy commitment
inferredcites →https://doi.org/10.4161/auto.8.2.18373openalex-snapshot
Atg4 recycles inappropriately lipidated Atg8 to promote autophagosome biogenesis

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.4753300openalex-extracted
Redox Regulation of Autophagy in Arabidopsis: Reactive Oxygen Species Differential Effects
inferred← citeshttps://doi.org/10.1002/1873-3468.14433openalex-snapshot
Hydrogen sulfide action in the regulation of plant autophagy
inferred← citeshttps://doi.org/10.1002/ijc.29990openalex-snapshot
Stress management by autophagy: Implications for chemoresistance
inferred← citeshttps://doi.org/10.1007/124_2017_6openalex-snapshot
Redox Control of Autophagy in Photosynthetic Organisms
inferred← citeshttps://doi.org/10.1007/978-1-0716-2079-3_17openalex-snapshot
Monitoring of ATG4 Protease Activity During Autophagy in the Model Microalga Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1007/978-3-030-73678-1_1openalex-snapshot
Hydrogen Sulfide on the Crossroad of Regulation, Protection, Interaction and Signaling in Plant Systems Under Different Environmental Conditions
inferred← citeshttps://doi.org/10.1007/978-3-319-40713-5_3openalex-snapshot
Regulation of Autophagy by Hydrogen Sulfide
inferred← citeshttps://doi.org/10.1007/s10340-023-01642-4openalex-snapshot
Abamectin induces mortality, inhibits food consumption, and causes histological changes in the midgut of the velvetbean caterpillar Anticarsia gemmatalis (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.1007/s11356-024-34010-5openalex-snapshot
Effects of the insecticide flupyradifurone on Anticarsia gemmatalis caterpillar and its predator Podisus nigrispinus
inferred← citeshttps://doi.org/10.1007/s11357-022-00717-xopenalex-snapshot
GTP energy dependence of endocytosis and autophagy in the aging brain and Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s12576-016-0507-7openalex-snapshot
Cardioprotection of exercise preconditioning involving heat shock protein 70 and concurrent autophagy: a potential chaperone-assisted selective macroautophagy effect
inferred← citeshttps://doi.org/10.1016/b978-0-12-821430-5.00016-xopenalex-snapshot
Photoproduction of reducing power and the Calvin-Benson cycle
inferred← citeshttps://doi.org/10.1016/bs.mie.2016.09.085openalex-snapshot
Monitoring the Formation of Autophagosomal Precursor Structures in Yeast Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/bs.mie.2016.10.024openalex-snapshot
Measurement of the Activity of the Atg4 Cysteine Proteases
inferred← citeshttps://doi.org/10.1016/bs.mie.2016.11.001openalex-snapshot
Tagged ATG8-Coding Constructs for the In Vitro and In Vivo Assessment of ATG4 Activity
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2015.09.001openalex-snapshot
8-Dehydrosterols induce membrane traffic and autophagy defects through V-ATPase dysfunction in Saccharomyces cerevisae
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.02.011openalex-snapshot
The vacuolar shapes of ageing: From function to morphology
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.bbapap.2016.02.006openalex-snapshot
Protein S-nitrosylation in photosynthetic organisms: A comprehensive overview with future perspectives
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.124585openalex-snapshot
Histopathological and cytotoxic changes induced by spinosad on midgut cells of the non-target predator Podisus nigrispinus Dallas (Heteroptera: Pentatomidae)
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.129439openalex-snapshot
Spiromesifen induces histopathological and cytotoxic changes in the midgut of the honeybee Apis mellifera (Hymenoptera: Apidae)
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.cotox.2018.12.007openalex-snapshot
Toxicant-mediated redox control of proteostasis in neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.08.030openalex-snapshot
Redox signaling: Potential arbitrator of autophagy and apoptosis in therapeutic response
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.09.026openalex-snapshot
Perturbation of redox balance after thioredoxin reductase deficiency interrupts autophagy-lysosomal degradation pathway and enhances cell death in nutritionally stressed SH-SY5Y cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.12.020openalex-snapshot
Modulation of signaling mechanisms in the heart by thioredoxin 1
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.04.004openalex-snapshot
Redox partner interactions in the ATG8 lipidation system in microalgae
inferred← citeshttps://doi.org/10.1016/j.gendis.2026.102098openalex-snapshot
The ATG4 isotype is a key regulator in CSE/H2S-mediated mitophagy in cardiac hypertrophy
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.06.069openalex-snapshot
Comparative proteomics of two citrus varieties in response to infection by the fungus Alternaria alternata
inferred← citeshttps://doi.org/10.1016/j.jgg.2021.05.005openalex-snapshot
ROS is essential for initiation of energy deprivation-induced autophagy
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.01.020openalex-snapshot
The pROS of Autophagy in Neuronal Health
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154671openalex-snapshot
Autophagy, ROS, and their interplay in plant adaptive responses
inferred← citeshttps://doi.org/10.1016/j.mad.2018.07.005openalex-snapshot
Stem cell rejuvenation and the role of autophagy in age retardation by caloric restriction: An update
inferred← citeshttps://doi.org/10.1016/j.mito.2020.01.002openalex-snapshot
Redox homeostasis, oxidative stress and mitophagy
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.molp.2016.09.012openalex-snapshot
The High Light Response and Redox Control of Thylakoid FtsH Protease in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1016/j.molp.2017.07.009openalex-snapshot
The Deep Thioredoxome in Chlamydomonas reinhardtii: New Insights into Redox Regulation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109800openalex-snapshot
Redox regulation of autophagy in Arabidopsis: The different ROS effects
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.redox.2024.103032openalex-snapshot
Thioredoxin (Trx): A redox target and modulator of cellular senescence and aging-related diseases
inferred← citeshttps://doi.org/10.1016/j.redox.2025.103852openalex-snapshot
An emerging role for cysteine-mediated redox signaling in aging
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/10.1038/ja.2017.104openalex-snapshot
Autophagy-regulating protease Atg4: structure, function, regulation and inhibition
inferred← citeshttps://doi.org/10.1038/s41380-019-0521-2openalex-snapshot
Thioredoxin-80 protects against amyloid-beta pathology through autophagic-lysosomal pathway regulation
inferred← citeshttps://doi.org/10.1038/s41418-018-0270-9openalex-snapshot
Loss of glutathione redox homeostasis impairs proteostasis by inhibiting autophagy-dependent protein degradation
inferred← citeshttps://doi.org/10.1038/s41418-023-01120-5openalex-snapshot
Mechanisms controlling plant proteases and their substrates
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/10.1039/9781782622888-00277openalex-snapshot
Protein Oxidation, Quality-Control Mechanisms and Parkinson’s Disease
inferred← citeshttps://doi.org/10.1073/pnas.2023604118openalex-snapshot
Persulfidation of ATG18a regulates autophagy under ER stress in Arabidopsis
inferred← citeshttps://doi.org/10.1080/15548627.2019.1709763openalex-snapshot
The protease activity of human ATG4B is regulated by reversible oxidative modification
inferred← citeshttps://doi.org/10.1080/15548627.2021.1984656openalex-snapshot
Full-coverage regulations of autophagy by ROS: from induction to maturation
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/10.1083/jcb.202002085openalex-snapshot
Autophagosome biogenesis: From membrane growth to closure
inferred← citeshttps://doi.org/10.1089/ars.2018.7617openalex-snapshot
Redox Homeostasis in Photosynthetic Organisms: Novel and Established Thiol-Based Molecular Mechanisms
inferred← citeshttps://doi.org/10.1089/ars.2021.0152openalex-snapshot
Oxidative Stress and Mitochondrial Dysfunction Associated with Peripheral Neuropathy in Type 1 Diabetes
inferred← citeshttps://doi.org/10.1091/mbc.e19-11-0622openalex-snapshot
Ubiquitin–proteasome-mediated cyclin C degradation promotes cell survival following nitrogen starvation
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/erab239openalex-snapshot
Hydrogen sulfide signaling in plant adaptations to adverse conditions: molecular mechanisms
inferred← citeshttps://doi.org/10.1093/jxb/erab383openalex-snapshot
Chlamydomonas proteases: classification, phylogeny, and molecular mechanisms
inferred← citeshttps://doi.org/10.1093/mutage/gey004openalex-snapshot
Role of cerium oxide nanoparticle-induced autophagy as a safeguard to exogenous H2O2-mediated DNA damage in tobacco BY-2 cells
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/10.1098/rstb.2023.0368openalex-snapshot
Evolutionary conservation and metabolic significance of autophagy in algae.
inferred← citeshttps://doi.org/10.1101/2022.09.01.506221openalex-snapshot
Quantitative proteomics and lipidomics of TFG-deficient B cells provide insights into mechanisms of autophagic flux and plasma cell biology
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/10.1101/2025.08.27.672299openalex-snapshot
Deciphering the role of autophagy under Cd toxicity in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1104/pp.15.01878openalex-snapshot
A light switch based on protein S-nitrosylation fine-tunes photosynthetic light-harvesting in the microalga Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1104/pp.16.00110openalex-snapshot
Negative regulation of autophagy by sulfide in Arabidopsis thaliana is independent of reactive oxygen species
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/10.1104/pp.18.00630openalex-snapshot
Chloroplast Damage Induced by the Inhibition of Fatty Acid Synthesis Triggers Autophagy in Chlamydomonas
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/10.1111/1440-1681.13764openalex-snapshot
Thioredoxin‐1 regulates the autophagy induced by oxidative stress through LC3‐II in human lens epithelial cells
inferred← citeshttps://doi.org/10.1111/nph.14627openalex-snapshot
Limited and digestive proteolysis: crosstalk between evolutionary conserved pathways
inferred← citeshttps://doi.org/10.1111/pce.13597openalex-snapshot
Cadmium induces reactive oxygen species‐dependent pexophagy in Arabidopsis leaves
inferred← citeshttps://doi.org/10.1128/aem.01321-20openalex-snapshot
The DUG Pathway Governs Degradation of Intracellular Glutathione in Aspergillus nidulans
inferred← citeshttps://doi.org/10.1155/2018/1916841openalex-snapshot
H2O2 Signaling‐Triggered PI3K Mediates Mitochondrial Protection to Participate in Early Cardioprotection by Exercise Preconditioning
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/10.1155/2020/8865611openalex-snapshot
Autophagy and Redox Homeostasis in Parkinson’s: A Crucial Balancing Act
inferred← citeshttps://doi.org/10.1242/jcs.158758openalex-snapshot
ERES: sites for autophagosome biogenesis and maturation?
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008047openalex-snapshot
The dynamin-like protein Fzl promotes thylakoid fusion and resistance to light stress in Chlamydomonas reinhardtii
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/10.1515/hsz-2024-0038openalex-snapshot
Protein persulfidation in plants: mechanisms and functions beyond a simple stress response
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/10.22268/ajpp-41.4.437443openalex-snapshot
Laboratory Study on Some Potential Histological Changes Induced by the Toxicity of a Mixed Insecticide (spinetoram + methoxyfenozide) on The Spiny Bollworm, Earias insulana
inferred← citeshttps://doi.org/10.3389/fcell.2018.00148openalex-snapshot
Identification of Kinases and Phosphatases That Regulate ATG4B Activity by siRNA and Small Molecule Screening in Cells
inferred← citeshttps://doi.org/10.3389/ffunb.2026.1881957openalex-snapshot
Hydrogen peroxide as a multifaceted regulator of the Atg4 protease and autophagy in the pathogenic fungus Alternaria alternata
inferred← citeshttps://doi.org/10.3389/fonc.2021.743703openalex-snapshot
Derivation and Clinical Validation of a Redox-Driven Prognostic Signature for Colorectal Cancer
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.2018.01369openalex-snapshot
Hydrogen Sulfide Signaling in Plants: Emerging Roles of Protein Persulfidation
inferred← citeshttps://doi.org/10.3389/fpls.2020.00772openalex-snapshot
High Light-Induced Nitric Oxide Production Induces Autophagy and Cell Death in Chlamydomonas reinhardtii
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/antiox11020304openalex-snapshot
How Cells Deal with the Fluctuating Environment: Autophagy Regulation under Stress in Yeast and Mammalian Systems
inferred← citeshttps://doi.org/10.3390/antiox14101222openalex-snapshot
PK11007 Covalently Inhibits Thioredoxin Reductase 1 to Induce Oxidative Stress and Autophagy Impairment in NSCLC Cells
inferred← citeshttps://doi.org/10.3390/antiox7110161openalex-snapshot
Cancer-Associated Function of 2-Cys Peroxiredoxin Subtypes as a Survival Gatekeeper
inferred← citeshttps://doi.org/10.3390/biology13030180openalex-snapshot
Insights into the Multifaceted Roles of Thioredoxin-1 System: Exploring Knockout Murine Models
inferred← citeshttps://doi.org/10.3390/biom10040650openalex-snapshot
Redox-Mediated Post-Translational Modifications of Proteolytic Enzymes and Their Role in Protease Functioning
inferred← citeshttps://doi.org/10.3390/cancers11050649openalex-snapshot
Targeting ATG4 in Cancer Therapy
inferred← citeshttps://doi.org/10.3390/cells11152262openalex-snapshot
Autophagy: A Key Regulator of Homeostasis and Disease: An Overview of Molecular Mechanisms and Modulators
inferred← citeshttps://doi.org/10.3390/cells6040036openalex-snapshot
Monitoring Autophagy in the Model Green Microalga Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.3390/cells8111307openalex-snapshot
When Unity Is Strength: The Strategies Used by Chlamydomonas to Survive Environmental Stresses
inferred← citeshttps://doi.org/10.3390/cells9010138openalex-snapshot
Mmi1, the Yeast Ortholog of Mammalian Translationally Controlled Tumor Protein (TCTP), Negatively Affects Rapamycin-Induced Autophagy in Post-Diauxic Growth Phase
inferred← citeshttps://doi.org/10.3390/ijms241813708openalex-snapshot
Yeast Lsm Pro-Apoptotic Mutants Show Defects in Autophagy
inferred← citeshttps://doi.org/10.3390/life13010098openalex-snapshot
Redox Regulation of Autophagy in Cancer: Mechanism, Prevention and Therapy
inferred← citeshttps://doi.org/10.3390/md18040191openalex-snapshot
Secondary Metabolites from the Culture of the Marine-derived Fungus Paradendryphiella salina PC 362H and Evaluation of the Anticancer Activity of Its Metabolite Hyalodendrin
inferred← citeshttps://doi.org/10.47328/ufvbbt.2023.475openalex-snapshot
Efeitos de inseticidas no aparelho digestivo de Anticarsia gemmatalis (Lepidoptera: Noctuidae) e seu predador Podisus nigrispinus (Heteroptera: Pentatomidae)
inferred← citeshttps://doi.org/10.64898/2026.05.04.722700openalex-snapshot
Dynamic Regulation of Atg4 Protease and Autophagy by Dithiothreitol and Iron in Alternaria alternata
inferred← citeshttps://doi.org/10.70675/ccc686dazb001z409dzbd2bz09d1409a0bdeopenalex-snapshot
Caractérisation des mécanismes contrôlant l’agrégation, un processus de défense contre le stress chez l’algue unicellulaire Chlamydomonas reinhardtii
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