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Nucleoredoxin guards against oxidative stress by protecting antioxidant enzymes

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What this work says

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

inferredcites →https://doi.org/10.1016/j.bbamcr.2006.08.017openalex-snapshot

Peroxisomes and aging

inferredcites →https://doi.org/10.1016/j.chom.2017.01.007openalex-snapshot

CATALASE2 Coordinates SA-Mediated Repression of Both Auxin Accumulation and JA Biosynthesis in Plant Defenses

inferredcites →https://doi.org/10.1016/j.cub.2014.03.034openalex-snapshot

ROS Function in Redox Signaling and Oxidative Stress

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2008.09.034openalex-snapshot

Detection of protein S-nitrosylation with the biotin-switch technique

inferredcites →https://doi.org/10.1016/j.jprot.2008.12.002openalex-snapshot

Thioredoxin targets in plants: The first 30 years

inferredcites →https://doi.org/10.1016/j.molcel.2011.11.027openalex-snapshot

Inactivation of a Peroxiredoxin by Hydrogen Peroxide Is Critical for Thioredoxin-Mediated Repair of Oxidized Proteins and Cell Survival

inferredcites →https://doi.org/10.1016/j.molcel.2014.08.003openalex-snapshot

Selective Protein Denitrosylation Activity of Thioredoxin-h5 Modulates Plant Immunity

inferredcites →https://doi.org/10.1016/j.taap.2008.06.004openalex-snapshot

Progeric effects of catalase inactivation in human cells

inferredcites →https://doi.org/10.1016/j.tibs.2015.05.001openalex-snapshot

Peroxiredoxins: guardians against oxidative stress and modulators of peroxide signaling

inferredcites →https://doi.org/10.1016/j.tplants.2011.03.007openalex-snapshot

ROS signaling: the new wave?

inferredcites →https://doi.org/10.1016/s0021-9258(18)47038-xopenalex-snapshot

Thioredoxin-dependent peroxide reductase from yeast.

inferredcites →https://doi.org/10.1016/s0021-9258(19)83562-7openalex-snapshot

Thioredoxin catalyzes the reduction of insulin disulfides by dithiothreitol and dihydrolipoamide.

inferredcites →https://doi.org/10.1016/s1360-1385(02)02312-9openalex-snapshot

Oxidative stress, antioxidants and stress tolerance

inferredcites →https://doi.org/10.1038/35041687openalex-snapshot

Oxidants, oxidative stress and the biology of ageing

inferredcites →https://doi.org/10.1038/35107108openalex-snapshot

Isochorismate synthase is required to synthesize salicylic acid for plant defence

inferredcites →https://doi.org/10.1038/nprot.2006.468openalex-snapshot

In-gel digestion for mass spectrometric characterization of proteins and proteomes

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot

Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana

inferredcites →https://doi.org/10.1073/pnas.191282098openalex-snapshot

Comprehensive survey of proteins targeted by chloroplast thioredoxin

inferredcites →https://doi.org/10.1073/pnas.96.24.14165openalex-snapshot

Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyperresponsive to pathogen infection

inferredcites →https://doi.org/10.1074/jbc.m110.106468openalex-snapshot

Nucleoredoxin Negatively Regulates Toll-like Receptor 4 Signaling via Recruitment of Flightless-I to Myeloid Differentiation Primary Response Gene (88)

inferredcites →https://doi.org/10.1089/ars.2008.2046openalex-snapshot

Evolution of Catalases from Bacteria to Humans

inferredcites →https://doi.org/10.1091/mbc.e02-06-0322openalex-snapshot

Peroxisome Senescence in Human Fibroblasts

inferredcites →https://doi.org/10.1093/aobpla/pls014openalex-snapshot

Hydrogen peroxide—a central hub for information flow in plant cells

inferredcites →https://doi.org/10.1093/emboj/16.16.4806openalex-snapshot

Catalase is a sink for H2O2 and is indispensable for stress defence in C3 plants

inferredcites →https://doi.org/10.1093/jxb/erq282openalex-snapshot

Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic models

inferredcites →https://doi.org/10.1093/mp/sst162openalex-snapshot

NTR/NRX Define a New Thioredoxin System in the Nucleus of Arabidopsis thaliana Cells

inferredcites →https://doi.org/10.1093/pcp/pch019openalex-snapshot

Target Proteins of the Cytosolic Thioredoxins in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/pcp/pcn038openalex-snapshot

Plant Catalase is Imported into Peroxisomes by Pex5p but is Distinct from Typical PTS1 Import

inferredcites →https://doi.org/10.1094/mpmi.2000.13.12.1380openalex-snapshot

Nitric Oxide Inhibition of Tobacco Catalase and Ascorbate Peroxidase

inferredcites →https://doi.org/10.1104/pp.105.067686openalex-snapshot

Ascorbic Acid Deficiency Activates Cell Death and Disease Resistance Responses in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.110.153957openalex-snapshot

Peroxisomal Hydrogen Peroxide Is Coupled to Biotic Defense Responses by ISOCHORISMATE SYNTHASE1 in a Daylength-Related Manner

inferredcites →https://doi.org/10.1104/pp.15.01930openalex-snapshot

The Thioredoxin GbNRX1 Plays a Crucial Role in Homeostasis of Apoplastic Reactive Oxygen Species in Response to Verticillium dahliae Infection in Cotton

inferredcites →https://doi.org/10.1105/tpc.105.033589openalex-snapshot

Redox Homeostasis and Antioxidant Signaling: A Metabolic Interface between Stress Perception and Physiological Responses

inferredcites →https://doi.org/10.1105/tpc.109.071225openalex-snapshot

Interplay between the NADP-Linked Thioredoxin and Glutathione Systems in Arabidopsis Auxin Signaling

inferredcites →https://doi.org/10.1105/tpc.15.00144openalex-snapshot

Arabidopsis CALCIUM-DEPENDENT PROTEIN KINASE8 and CATALASE3 Function in Abscisic Acid-Mediated Signaling and H2O2 Homeostasis in Stomatal Guard Cells under Drought Stress

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02617.xopenalex-snapshot

Gateway‐compatible vectors for plant functional genomics and proteomics

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03263.xopenalex-snapshot

Conditional oxidative stress responses in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of daylength‐dependent gene expression, and define photoperiod as a crucial factor in the regulation of H 2 O 2 ‐induced cell death

inferredcites →https://doi.org/10.1111/j.1432-1033.1995.tb20798.xopenalex-snapshot

Reversible Binding and Inhibition of Catalase by Nitric Oxide

inferredcites →https://doi.org/10.1111/pce.12053openalex-snapshot

Down‐regulation of catalase activity allows transient accumulation of a hydrogen peroxide signal in C hlamydomonas reinhardtii

inferredcites →https://doi.org/10.1111/tra.12129openalex-snapshot

PEX5 , the Shuttling Import Receptor for Peroxisomal Matrix Proteins, Is a Redox‐Sensitive Protein

inferredcites →https://doi.org/10.1126/science.1156970openalex-snapshot

Plant Immunity Requires Conformational Charges of NPR1 via S-Nitrosylation and Thioredoxins

inferredcites →https://doi.org/10.1126/science.1158265openalex-snapshot

Regulated Protein Denitrosylation by Cytosolic and Mitochondrial Thioredoxins

inferredcites →https://doi.org/10.1146/annurev-genet-102108-134201openalex-snapshot

Thioredoxins and Glutaredoxins: Unifying Elements in Redox Biology

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

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miRNAs and their target genes regulate the antioxidant system of Zanthoxylum bungeanum under drought stress

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inferred← citeshttps://doi.org/10.3389/fpls.2021.672672openalex-snapshot

Mutual Promotion of LAP2 and CAT2 Synergistically Regulates Plant Salt and Osmotic Stress Tolerance

inferred← citeshttps://doi.org/10.3389/fpls.2021.711853openalex-snapshot

Molecular and Biochemical Insights Into Early Responses of Hemp to Cd and Zn Exposure and the Potential Effect of Si on Stress Response

inferred← citeshttps://doi.org/10.3389/fpls.2021.733237openalex-snapshot

The Powdery Mildew Effector CSEP0027 Interacts With Barley Catalase to Regulate Host Immunity

inferred← citeshttps://doi.org/10.3389/fpls.2021.756338openalex-snapshot

Nucleoredoxin Gene TaNRX1 Positively Regulates Drought Tolerance in Transgenic Wheat (Triticum aestivum L.)

inferred← citeshttps://doi.org/10.3389/fpls.2021.768693openalex-snapshot

Integrative Proteomic and Phosphoproteomic Analyses of Pattern- and Effector-Triggered Immunity in Tomato

inferred← citeshttps://doi.org/10.3389/fpls.2022.1015317openalex-snapshot

Grafting enhances plants drought resistance: Current understanding, mechanisms, and future perspectives

inferred← citeshttps://doi.org/10.3389/fpls.2022.1020584openalex-snapshot

Genome-wide identification, characterization, evolution, and expression pattern analyses of the typical thioredoxin gene family in wheat (Triticum aestivum L.)

inferred← citeshttps://doi.org/10.3389/fpls.2022.1035573openalex-snapshot

Protein-protein interactions in plant antioxidant defense

inferred← citeshttps://doi.org/10.3389/fpls.2022.946037openalex-snapshot

Genome-wide identification of foxtail millet’s TRX family and a functional analysis of SiNRX1 in response to drought and salt stresses in transgenic Arabidopsis

inferred← citeshttps://doi.org/10.3389/fpls.2025.1562718openalex-snapshot

Genome-wide identification of the nuclear redox protein gene family revealed its potential role in drought stress tolerance in rice

inferred← citeshttps://doi.org/10.3389/fpls.2025.1701035openalex-snapshot

Physiological and molecular mechanisms of drought adaptation in foxtail millet: insights and future perspectives

inferred← citeshttps://doi.org/10.3390/antiox11040670openalex-snapshot

Is Nucleoredoxin a Master Regulator of Cellular Redox Homeostasis? Its Implication in Different Pathologies

inferred← citeshttps://doi.org/10.3390/antiox11061106openalex-snapshot

Nucleoredoxin Plays a Key Role in the Maintenance of Retinal Pigmented Epithelium Differentiation

inferred← citeshttps://doi.org/10.3390/antiox11081622openalex-snapshot

Analysis of Thioredoxins and Glutaredoxins in Soybean: Evidence of Translational Regulation under Water Restriction

inferred← citeshttps://doi.org/10.3390/antiox13030257openalex-snapshot

Nucleoredoxin Redox Interactions Are Sensitized by Aging and Potentiated by Chronic Alcohol Consumption in the Mouse Liver

inferred← citeshttps://doi.org/10.3390/antiox13030315openalex-snapshot

Complex Formation between the Transcription Factor WRKY53 and Antioxidative Enzymes Leads to Reciprocal Inhibition

inferred← citeshttps://doi.org/10.3390/antiox8010016openalex-snapshot

Cytosolic Isocitrate Dehydrogenase from Arabidopsis thaliana Is Regulated by Glutathionylation

inferred← citeshttps://doi.org/10.3390/ijms21239196openalex-snapshot

Redox-Dependent Structural Modification of Nucleoredoxin Triggers Defense Responses against Alternaria brassicicola in Arabidopsis

inferred← citeshttps://doi.org/10.3390/ijms21249706openalex-snapshot

Distinct Preflowering Drought Tolerance Strategies of Sorghum bicolor Genotype RTx430 Revealed by Subcellular Protein Profiling

inferred← citeshttps://doi.org/10.3390/ijms24054530openalex-snapshot

Genetic Adaptation of Siberian Larch (Larix sibirica Ledeb.) to High Altitudes

inferred← citeshttps://doi.org/10.3390/ijms25073783openalex-snapshot

Genome-Wide Identification and Expression Profiling of the ABF Transcription Factor Family in Wheat (Triticum aestivum L.)

inferred← citeshttps://doi.org/10.3390/molecules24183231openalex-snapshot

Cyanate Induces Oxidative Stress Injury and Abnormal Lipid Metabolism in Liver through Nrf2/HO-1

inferred← citeshttps://doi.org/10.3390/plants14142101openalex-snapshot

Genome-Wide Characterization of VDAC Gene Family in Soybean (Glycine max L.) and In Silico Expression Profiling in Response to Drought and Salt Stress

inferred← citeshttps://doi.org/10.3390/plants15010146openalex-snapshot

The Wheat Nucleoredoxin TaNRX1-2D Gene Ameliorates Salt Tolerance in Wheat (Triticum aestivum L.)

inferred← citeshttps://doi.org/10.3390/targets2030012openalex-snapshot

Review of Hydrogen Sulfide Based on Its Activity Mechanism and Fluorescence Sensing

inferred← citeshttps://doi.org/10.70675/30d5147ezdd87z449dzb519z6daa1055a2a5openalex-snapshot

La glutarédoxine GRXS17, une chaperonne redox-dépendante impliquée dans le développement des racines et dans la thermotolérance chez Arabidopsis thaliana

inferred← citeshttps://doi.org/10.70675/40f401b4z5e3cz4dfaza070z77c95a145f2eopenalex-snapshot

Glutathione and glutaredoxins, major regulators of root system architecture

inferred← citeshttps://doi.org/10.70675/f30f06dez9306z4439z9e54zf1cc1e16e1a4openalex-snapshot

Evaluation de la réponse cellulaire et moléculaire d'une diatomée benthique d'eau douce à l'exposition à des nanoparticules carbonées

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