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NO signaling in plant immunity: A tale of messengers

https://doi.org/10.1016/j.phytochem.2014.03.015

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What this work says

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

inferredcites →https://doi.org/10.1111/pce.12295zenodo-depositor-declared

Interplays between nitric oxide and reactive oxygen species in cryptogein signalling

inferredcites →https://doi.org/10.1002/elps.200800826openalex-snapshot

Protein nitration during defense response in Arabidopsis thaliana

inferredcites →https://doi.org/10.1002/pmic.200700536openalex-snapshot

Proteomic analysis of S‐nitrosylated proteins in Arabidopsis thaliana undergoing hypersensitive response

inferredcites →https://doi.org/10.1002/pmic.201200237openalex-snapshot

Plant proteins under oxidative attack

inferredcites →https://doi.org/10.1007/s00299-013-1434-1openalex-snapshot

Nitric oxide as a key component in hormone-regulated processes

inferredcites →https://doi.org/10.1007/s00425-008-0855-5openalex-snapshot

Nitric oxide production occurs downstream of reactive oxygen species in guard cells during stomatal closure induced by chitosan in abaxial epidermis of Pisum sativum

inferredcites →https://doi.org/10.1016/j.bbagen.2011.10.012openalex-snapshot

Analysis of calcium signaling pathways in plants

inferredcites →https://doi.org/10.1016/j.bbagen.2013.07.002openalex-snapshot

Inhibition of peroxisomal hydroxypyruvate reductase (HPR1) by tyrosine nitration

inferredcites →https://doi.org/10.1016/j.bbamcr.2008.01.015openalex-snapshot

Mechanisms of Cdc48/VCP-mediated cell death — from yeast apoptosis to human disease

inferredcites →https://doi.org/10.1016/j.biochi.2011.04.006openalex-snapshot

Involvement of putative glutamate receptors in plant defence signaling and NO production

inferredcites →https://doi.org/10.1016/j.biochi.2011.07.012openalex-snapshot

Calmodulin and calmodulin-like proteins in plant calcium signaling

inferredcites →https://doi.org/10.1016/j.cellsig.2010.08.003openalex-snapshot

The diverse functions of GAPDH: Views from different subcellular compartments

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2005.12.006openalex-snapshot

Mechanisms of nitric-oxide-induced increase of free cytosolic Ca2+ concentration in Nicotiana plumbaginifolia cells

inferredcites →https://doi.org/10.1016/j.gene.2013.05.056openalex-snapshot

Functional characterization of the plant ubiquitin regulatory X (UBX) domain-containing protein AtPUX7 in Arabidopsis thaliana

inferredcites →https://doi.org/10.1016/j.niox.2011.01.009openalex-snapshot

Detection of peroxynitrite accumulation in Arabidopsis thaliana during the hypersensitive defense response

inferredcites →https://doi.org/10.1016/j.pbi.2009.05.012openalex-snapshot

NO signals in the hazeNitric oxide signalling in plant defence

inferredcites →https://doi.org/10.1016/j.pbi.2010.04.002openalex-snapshot

Ubiquitination in plant immunity

inferredcites →https://doi.org/10.1016/j.pbi.2011.07.005openalex-snapshot

Upstream and downstream signals of nitric oxide in pathogen defence

inferredcites →https://doi.org/10.1016/j.plantsci.2009.06.006openalex-snapshot

Current view of nitric oxide-responsive genes in plants

inferredcites →https://doi.org/10.1016/j.plantsci.2011.04.005openalex-snapshot

Nitric oxide imbalance provokes a nitrosative response in plants under abiotic stress

inferredcites →https://doi.org/10.1016/j.plantsci.2011.05.002openalex-snapshot

Peroxynitrite formation and function in plants

inferredcites →https://doi.org/10.1016/j.plaphy.2005.07.012openalex-snapshot

Proteomic identification of glyceraldehyde 3-phosphate dehydrogenase as an inhibitory target of hydrogen peroxide in Arabidopsis

inferredcites →https://doi.org/10.1016/j.tplants.2005.07.001openalex-snapshot

Handling calcium signaling: Arabidopsis CaMs and CMLs

inferredcites →https://doi.org/10.1016/s0092-8674(01)00495-0openalex-snapshot

Nitrosylation

inferredcites →https://doi.org/10.1016/s0959-440x(00)00142-1openalex-snapshot

EF-hand calcium-binding proteins

inferredcites →https://doi.org/10.1021/cb800279qopenalex-snapshot

Chemical Biology of Peroxynitrite: Kinetics, Diffusion, and Radicals

inferredcites →https://doi.org/10.1038/29087openalex-snapshot

Nitric oxide functions as a signal in plant disease resistance

inferredcites →https://doi.org/10.1038/364450a0openalex-snapshot

Amplification of calcium-induced gene transcription by nitric oxide in neuronal cells

inferredcites →https://doi.org/10.1038/70249openalex-snapshot

Coordination of calcium signalling by endothelial-derived nitric oxide in the intact liver

inferredcites →https://doi.org/10.1038/nature10427openalex-snapshot

S-nitrosylation of NADPH oxidase regulates cell death in plant immunity

inferredcites →https://doi.org/10.1038/nature12478openalex-snapshot

GLUTAMATE RECEPTOR-LIKE genes mediate leaf-to-leaf wound signalling

inferredcites →https://doi.org/10.1038/ncb0805-742openalex-snapshot

Delivery of ubiquitinated substrates to protein-unfolding machines

inferredcites →https://doi.org/10.1038/ncb1268openalex-snapshot

S-nitrosylated GAPDH initiates apoptotic cell death by nuclear translocation following Siah1 binding

inferredcites →https://doi.org/10.1038/ncb2114openalex-snapshot

GAPDH mediates nitrosylation of nuclear proteins

inferredcites →https://doi.org/10.1038/ncb2407openalex-snapshot

Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system

inferredcites →https://doi.org/10.1042/bj20100492openalex-snapshot

Regulation of Nicotiana tabacum osmotic stress-activated protein kinase and its cellular partner GAPDH by nitric oxide in response to salinity

inferredcites →https://doi.org/10.1042/bj20111112openalex-snapshot

Ionotropic glutamate receptor (iGluR)-like channels mediate MAMP-induced calcium influx in Arabidopsis thaliana

inferredcites →https://doi.org/10.1042/bj20120257openalex-snapshot

Nitric oxide inhibits the ATPase activity of the chaperone-like AAA+ ATPase CDC48, a target for S-nitrosylation in cryptogein signalling in tobacco cells

inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00835.xopenalex-snapshot

In vivo imaging of an elicitor‐induced nitric oxide burst in tobacco

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00984.xopenalex-snapshot

Effects of urate, a natural inhibitor of peroxynitrite‐mediated toxicity, in the response of Arabidopsis thaliana to the bacterial pathogen Pseudomonas syringae

inferredcites →https://doi.org/10.1046/j.1432-1327.2001.02301.xopenalex-snapshot

Transcriptionally and post‐transcriptionally regulated response of 13 calmodulin genes to tobacco mosaic virus‐induced cell death and wounding in tobacco plant

inferredcites →https://doi.org/10.1073/pnas.1205448109openalex-snapshot

Linking ligand perception by PEPR pattern recognition receptors to cytosolic Ca 2+ elevation and downstream immune signaling in plants

inferredcites →https://doi.org/10.1073/pnas.1210659109openalex-snapshot

AAA ATPase p97/VCP is essential for TRIM21-mediated virus neutralization

inferredcites →https://doi.org/10.1073/pnas.1434381100openalex-snapshot

Nitric oxide regulates K + and Cl - channels in guard cells through a subset of abscisic acid-evoked signaling pathways

inferredcites →https://doi.org/10.1073/pnas.95.17.10328openalex-snapshot

Defense gene induction in tobacco by nitric oxide, cyclic GMP, and cyclic ADP-ribose

inferredcites →https://doi.org/10.1074/jbc.271.7.3699openalex-snapshot

Nitric Oxide-induced Mobilization of Intracellular Calcium via the Cyclic ADP-ribose Signaling Pathway

inferredcites →https://doi.org/10.1074/jbc.m110.135236openalex-snapshot

Temperature-sensitive Post-translational Regulation of Plant Omega-3 Fatty-acid Desaturases Is Mediated by the Endoplasmic Reticulum-associated Degradation Pathway

inferredcites →https://doi.org/10.1074/jbc.m113.475467openalex-snapshot

Mechanisms of Nitrosylation and Denitrosylation of Cytoplasmic Glyceraldehyde-3-phosphate Dehydrogenase from Arabidopsis thaliana

inferredcites →https://doi.org/10.1074/jbc.m509700200openalex-snapshot

ATPase Activity of p97/Valosin-containing Protein Is Regulated by Oxidative Modification of the Evolutionally Conserved Cysteine 522 Residue in Walker A Motif

inferredcites →https://doi.org/10.1074/jbc.m709316200openalex-snapshot

The Role of CDC48 in the Retro-translocation of Non-ubiquitinated Toxin Substrates in Plant Cells

inferredcites →https://doi.org/10.1074/jbc.m806782200openalex-snapshot

S-Nitrosylation of AtSABP3 Antagonizes the Expression of Plant Immunity

inferredcites →https://doi.org/10.1074/jbc.r113.472936openalex-snapshot

Peroxynitrite, a Stealthy Biological Oxidant

inferredcites →https://doi.org/10.1089/ars.2012.5066openalex-snapshot

Specificity in S-Nitrosylation: A Short-Range Mechanism for NO Signaling?

inferredcites →https://doi.org/10.1089/ars.2012.5136openalex-snapshot

Hydrogen Peroxide and Nitric Oxide: Key Regulators of the Legume— Rhizobium and Mycorrhizal Symbioses

inferredcites →https://doi.org/10.1089/ars.2013.5679openalex-snapshot

Redox Regulation in Plant Immune Function

inferredcites →https://doi.org/10.1093/jxb/erm197openalex-snapshot

Nitric oxide signalling in plants: interplays with Ca2+ and protein kinases

inferredcites →https://doi.org/10.1093/jxb/err414openalex-snapshot

S-Nitrosylated proteins in pea (Pisum sativum L.) leaf peroxisomes: changes under abiotic stress

inferredcites →https://doi.org/10.1093/jxb/ers031openalex-snapshot

The soluble proteome of tobacco Bright Yellow-2 cells undergoing H2O2-induced programmed cell death

inferredcites →https://doi.org/10.1093/mp/ssm016openalex-snapshot

Nitric Oxide in Plants: Production and Cross-talk with Ca2+ Signaling

inferredcites →https://doi.org/10.1093/pcp/pcj038openalex-snapshot

Peroxynitrite Generation and Tyrosine Nitration in Defense Responses in Tobacco BY-2 Cells

inferredcites →https://doi.org/10.1093/pcp/pcm011openalex-snapshot

Pathogen-Induced Calmodulin Isoforms in Basal Resistance Against Bacterial and Fungal Pathogens in Tobacco

inferredcites →https://doi.org/10.1094/mpmi-09-12-0214-cropenalex-snapshot

Nitric Oxide as a Mediator for Defense Responses

inferredcites →https://doi.org/10.1094/mpmi-19-0429openalex-snapshot

Integrated Signaling Network Involving Calcium, Nitric Oxide, and Active Oxygen Species but Not Mitogen-Activated Protein Kinases in BcPG1-Elicited Grapevine Defenses

inferredcites →https://doi.org/10.1094/mpmi-22-6-0619openalex-snapshot

Nitric Oxide as a Partner of Reactive Oxygen Species Participates in Disease Resistance to Necrotrophic Pathogen Botrytis cinerea in Nicotiana benthamiana

inferredcites →https://doi.org/10.1094/mpmi-23-7-0846openalex-snapshot

Nitric Oxide Participates in the Complex Interplay of Defense-Related Signaling Pathways Controlling Disease Resistance to Sclerotinia sclerotiorum in Arabidopsis thaliana

inferredcites →https://doi.org/10.1094/mpmi.2004.17.3.245openalex-snapshot

Nitric Oxide and Reactive Oxygen Species Do Not Elicit Hypersensitive Cell Death but Induce Apoptosis in the Adjacent Cells During the Defense Response of Oat

inferredcites →https://doi.org/10.1104/pp.104.038968openalex-snapshot

Analysis of Nitric Oxide Signaling Functions in Tobacco Cells Challenged by the Elicitor Cryptogein

inferredcites →https://doi.org/10.1104/pp.104.058719openalex-snapshot

Proteomic Identification of S -Nitrosylated Proteins in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.106.078444openalex-snapshot

Nitric Oxide- and Hydrogen Peroxide-Responsive Gene Regulation during Cell Death Induction in Tobacco

inferredcites →https://doi.org/10.1104/pp.108.121897openalex-snapshot

In Planta Analysis of the Cell Cycle-Dependent Localization of AtCDC48A and Its Critical Roles in Cell Division, Expansion, and Differentiation

inferredcites →https://doi.org/10.1104/pp.108.125104openalex-snapshot

Innate Immunity Signaling: Cytosolic Ca2+ Elevation Is Linked to Downstream Nitric Oxide Generation through the Action of Calmodulin or a Calmodulin-Like Protein

inferredcites →https://doi.org/10.1104/pp.111.184531openalex-snapshot

Nitric Oxide and ProteinS-Nitrosylation Are Integral to Hydrogen Peroxide-Induced Leaf Cell Death in Rice

inferredcites →https://doi.org/10.1104/pp.112.194472openalex-snapshot

SNF1-Related Protein Kinases Type 2 Are Involved in Plant Responses to Cadmium Stress

inferredcites →https://doi.org/10.1104/pp.112.207399openalex-snapshot

Control of Tobacco mosaic virus Movement Protein Fate by CELL-DIVISION-CYCLE Protein48

inferredcites →https://doi.org/10.1104/pp.113.217208openalex-snapshot

Glutamate Receptor-Like Channel3.3 Is Involved in Mediating Glutathione-Triggered Cytosolic Calcium Transients, Transcriptional Changes, and Innate Immunity Responses in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.113.220624openalex-snapshot

There's More to the Picture Than Meets the Eye: Nitric Oxide Cross Talk with Ca2+ Signaling

inferredcites →https://doi.org/10.1104/pp.113.222703openalex-snapshot

S-Nitrosylation of Ascorbate Peroxidase Is Part of Programmed Cell Death Signaling in Tobacco Bright Yellow-2 Cells

inferredcites →https://doi.org/10.1104/pp.113.226068openalex-snapshot

Molecular Steps in the Immune Signaling Pathway Evoked by Plant Elicitor Peptides: Ca2+-Dependent Protein Kinases, Nitric Oxide, and Reactive Oxygen Species Are Downstream from the Early Ca2+ Signal

inferredcites →https://doi.org/10.1105/tpc.104.026625openalex-snapshot

Conserved ERAD-Like Quality Control of a Plant Polytopic Membrane Protein

inferredcites →https://doi.org/10.1105/tpc.106.045096openalex-snapshot

Death Don't Have No Mercy and Neither Does Calcium: Arabidopsis CYCLIC NUCLEOTIDE GATED CHANNEL2 and Innate Immunity

inferredcites →https://doi.org/10.1105/tpc.107.055061openalex-snapshot

S-Nitrosylation of Peroxiredoxin II E Promotes Peroxynitrite-Mediated Tyrosine Nitration

inferredcites →https://doi.org/10.1105/tpc.109.066464openalex-snapshot

Redox Regulation of the NPR1-TGA1 System of Arabidopsis thaliana by Nitric Oxide

inferredcites →https://doi.org/10.1105/tpc.112.096768openalex-snapshot

Oleic Acid–Dependent Modulation of NITRIC OXIDE ASSOCIATED1 Protein Levels Regulates Nitric Oxide–Mediated Defense Signaling in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-3040.2012.02505.xopenalex-snapshot

Nitric oxide production mediates oligogalacturonide‐triggered immunity and resistance to Botrytis cinerea in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02471.xopenalex-snapshot

Protein phosphorylation is a prerequisite for intracellular Ca2+release and ion channel control by nitric oxide and abscisic acid in guard cells

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04000.xopenalex-snapshot

Proteomics reveals the overlapping roles of hydrogen peroxide and nitric oxide in the acclimation of citrus plants to salinity

inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01308.xopenalex-snapshot

NO synthesis and signaling in plants – where do we stand?

inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01777.xopenalex-snapshot

Calcium in plant defence‐signalling pathways

inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03577.xopenalex-snapshot

Ca2+ conduction by plant cyclic nucleotide gated channels and associated signaling components in pathogen defense signal transduction cascades

inferredcites →https://doi.org/10.1111/tpj.12311openalex-snapshot

Involvement of the glutamate receptor A t GLR 3.3 in plant defense signaling and resistance to H yaloperonospora arabidopsidis

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.1281928openalex-snapshot

Biochemistry of Nitric Oxide and Its Redox-Activated Forms

inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092830openalex-snapshot

New Insights into Nitric Oxide Signaling in Plants

inferredcites →https://doi.org/10.1155/2013/183421openalex-snapshot

Cdc48: A Swiss Army Knife of Cell Biology

inferredcites →https://doi.org/10.1371/journal.ppat.1000301openalex-snapshot

Arabidopsis CaM Binding Protein CBP60g Contributes to MAMP-Induced SA Accumulation and Is Involved in Disease Resistance against Pseudomonas syringae

inferredcites →https://doi.org/10.3389/fpls.2013.00137openalex-snapshot

Nitric oxide-based protein modification: formation and site-specificity of protein S-nitrosylation

inferredcites →https://doi.org/10.3389/fpls.2013.00314openalex-snapshot

Cross-talk of nitric oxide and reactive oxygen species in plant programed cell death

inferredcites →https://doi.org/10.4161/psb.4.3.8256openalex-snapshot

Nitric oxide triggers specific and dose-dependent cytosolic calcium transients in Arabidopsis

What points at this work

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

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Plant Nitric Oxide Signaling Under Environmental Stresses

inferred← citeshttps://doi.org/10.1002/9781119468677.ch23openalex-snapshot

Reactive Oxygen Species and Nitric Oxide Production, Regulation and Function During Defense Response

inferred← citeshttps://doi.org/10.1002/9781119803041.ch3openalex-snapshot

Role of Nutrients in the ROS Metabolism in Plants

inferred← citeshttps://doi.org/10.1002/ceat.201600691openalex-snapshot

Detection of Copper Bisguanidine NO Adducts by UV‐vis Spectroscopy and a SuperFocus Mixer

inferred← citeshttps://doi.org/10.1002/jsfa.13875openalex-snapshot

Exogenous nitric oxide treatment delays the senescence of postharvest mung bean sprouts by regulating ascorbic acid metabolism

inferred← citeshttps://doi.org/10.1002/ppp3.70025openalex-snapshot

Plasma‐activated water to foster sustainable agriculture: Evidence and quest for the fundamentals

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Laser-Based Methods for Detection of Nitric Oxide in Plants

inferred← citeshttps://doi.org/10.1007/978-3-030-11129-8_3openalex-snapshot

Hydrogen Peroxide (H2O2)- and Nitric Oxide (NO)-Derived Posttranslational Modifications

inferred← citeshttps://doi.org/10.1007/978-3-030-77477-6_1openalex-snapshot

Plant Hormones and Plant Defense Response Against Pathogens

inferred← citeshttps://doi.org/10.1007/978-3-030-78420-1_10openalex-snapshot

New Insights into the Functional Role of Nitric Oxide and Reactive Oxygen Species in Plant Response to Biotic and Abiotic Stress Conditions

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Plant-Microbe Interactions: A Molecular Approach

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Dual stress (waterlogging and salinity) resilience in Arabidopsis thaliana conferred by overexpression of a putative daylily (Hemerocallis spp.) betaine aldehyde dehydrogenase gene

inferred← citeshttps://doi.org/10.1007/s10535-017-0706-yopenalex-snapshot

Cytosolic GAPDH: a key mediator in redox signal transduction in plants

inferred← citeshttps://doi.org/10.1007/s10658-018-1551-3openalex-snapshot

Effect of natural and synthetic Brassinosteroids on strawberry immune response against Colletotrichum acutatum

inferred← citeshttps://doi.org/10.1007/s11738-015-1949-xopenalex-snapshot

Paclitaxel production and PAL activity in hairy root cultures of Taxus x media var. Hicksii carrying a taxadiene synthase transgene elicited with nitric oxide and methyl jasmonate

inferred← citeshttps://doi.org/10.1007/s40626-023-00289-xopenalex-snapshot

Protein S-nitrosylation in plants under biotic stress

inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00010-8openalex-snapshot

Metabolic Responses of Plants Upon Different Plant–Pathogen Interactions

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Plant–microbe interactions: perspectives in promoting plant health

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The Role of Nitric Oxide in Development and Pathogenesis of Biotrophic Phytopathogens – Downy and Powdery Mildews

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Nitric Oxide and Reactive Oxygen Species in PCD Signaling

inferred← citeshttps://doi.org/10.1016/bs.abr.2015.10.013openalex-snapshot

Nitric Oxide Signaling during the Hypersensitive Disease Resistance Response

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Protein S-nitrosylation in photosynthetic organisms: A comprehensive overview with future perspectives

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Physiological and proteomic mechanisms of waterlogging priming improves tolerance to waterlogging stress in wheat ( Triticum aestivum L.)

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Abscisic acid plays a pivotal role in stomatal defense at the early infection of Verticillium dahliae in Gossypium hirsutum

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Expanding roles for S-nitrosylation in the regulation of plant immunity

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Interactions between second messengers, SA and MAPK6 signaling pathways lead to chitosan-induced lignan production in Linum album cell culture

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The Deep Thioredoxome in Chlamydomonas reinhardtii: New Insights into Redox Regulation

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Nitric oxide as a secondary messenger during stomatal closure as a part of plant immunity response against pathogens

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An update on nitric oxide and its benign role in plant responses under metal stress

inferred← citeshttps://doi.org/10.1016/j.niox.2018.09.004openalex-snapshot

Proteomics analysis reveals that nitric oxide regulates photosynthesis of maize seedlings under water deficiency

inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.09.019openalex-snapshot

The NOS-like protein from the microalgae Ostreococcus tauri is a genuine and ultrafast NO-producing enzyme

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.03.004openalex-snapshot

Mutual interplay of Ca2+ and ROS signaling in plant immune response

inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112472openalex-snapshot

Nitric oxide production and protein S-nitrosation in algae

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POLYAMINE OXIDASE2 of Arabidopsis contributes to ABA mediated plant developmental processes

inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.06.012openalex-snapshot

Nitric oxide mitigates the effect of water deficit in Crambe abyssinica

inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110427openalex-snapshot

Turtlegrass (Thalassia testudinum) undergoes a coordinated hypersensitive response when challenged with pathogenic Labyrinthula sp.

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Antioxidant enzymes regulation in plants in reference to reactive oxygen species (ROS) and reactive nitrogen species (RNS)

inferred← citeshttps://doi.org/10.1016/j.pmpp.2020.101503openalex-snapshot

Nitric oxide improves tolerance to Fusarium oxysporum f. sp. cubense Tropical Race 4 in banana

inferred← citeshttps://doi.org/10.1016/j.postharvbio.2026.114451openalex-snapshot

Strigolactone treatment enhances resistance to black spot in korla fragrant pear by activating Ca2 + /NO signaling and maintaining reactive oxygen species homeostasis

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Screening and functional characterization of Rehmannia glutinosa receptor proteins (RgRLPs) in response to continuous cropping stress

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Mechanisms of nitric oxide involvement in plant-microbe interaction and its enhancement of stress resistance

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A nitric oxide burst at the shoot apex triggers a heat-responsive pathway in Arabidopsis

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Comparative metabolomic analysis highlights the involvement of sugars and glycerol in melatonin-mediated innate immunity against bacterial pathogen in Arabidopsis

inferred← citeshttps://doi.org/10.1080/09168451.2016.1179091openalex-snapshot

Endogenous nitric oxide mediates He-Ne laser-induced adaptive responses in salt stressed-tall fescue leaves

inferred← citeshttps://doi.org/10.1080/11263504.2025.2554071openalex-snapshot

Shaping intracellular calcium signatures associated with environmental stresses by plasma-activated water in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1080/15592324.2017.1296997openalex-snapshot

Plant signals during beetle (Scolytus multistriatus) feeding in American elm (Ulmus americanaPlanch)

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/10.1093/jxb/eraa421openalex-snapshot

Nitric oxide production and signalling in algae

inferred← citeshttps://doi.org/10.1093/jxb/eraa470openalex-snapshot

Nitric oxide signalling in plant nanobiology: current status and perspectives

inferred← citeshttps://doi.org/10.1093/jxb/erv099openalex-snapshot

ROS and RNS in plant physiology: an overview

inferred← citeshttps://doi.org/10.1093/jxb/erz031openalex-snapshot

Nitric oxide and hydrogen sulfide in plants: which comes first?

inferred← citeshttps://doi.org/10.1093/jxb/erz289openalex-snapshot

Nitric oxide in plant–fungal interactions

inferred← citeshttps://doi.org/10.1093/plphys/kiab222openalex-snapshot

Nitric oxide coordinates growth, development, and stress response via histone modification and gene expression

inferred← citeshttps://doi.org/10.1101/2020.06.16.154476openalex-snapshot

Nitric oxide coordinates histone acetylation and expression of genes involved in growth/development and stress response

inferred← citeshttps://doi.org/10.1104/pp.15.00551openalex-snapshot

Spore Density Determines Infection Strategy by the Plant Pathogenic Fungus Plectosphaerella cucumerina

inferred← citeshttps://doi.org/10.1104/pp.15.01378openalex-snapshot

Update: Post-translational protein modifications in plant metabolism

inferred← citeshttps://doi.org/10.1104/pp.16.00780openalex-snapshot

NAD Acts as an Integral Regulator of Multiple Defense Layers

inferred← citeshttps://doi.org/10.1105/tpc.16.00557openalex-snapshot

Host-Mediated S-Nitrosylation Disarms the Bacterial Effector HopAI1 to Reestablish Immunity

inferred← citeshttps://doi.org/10.1111/aab.12657openalex-snapshot

Hypersensitive response: From NLR pathogen recognition to cell death response

inferred← citeshttps://doi.org/10.1111/efp.12486openalex-snapshot

Response of in vitro obtained oil palm and interspecific OxG hybrids to inoculation with Phytophthora palmivora

inferred← citeshttps://doi.org/10.1111/jipb.12780openalex-snapshot

Protein S‐Nitrosylation in plants: Current progresses and challenges

inferred← citeshttps://doi.org/10.1111/jpi.12244openalex-snapshot

Melatonin induces nitric oxide and the potential mechanisms relate to innate immunity against bacterial pathogen infection in Arabidopsis

inferred← citeshttps://doi.org/10.1111/mpp.13445openalex-snapshot

Natural variation in the pattern‐triggered immunity response in plants: Investigations, implications and applications

inferred← citeshttps://doi.org/10.1111/pbi.13505openalex-snapshot

The dual interplay of RAV5 in activating nitrate reductases and repressing catalase activity to improve disease resistance in cassava

inferred← citeshttps://doi.org/10.1111/pbi.13663openalex-snapshot

A rice LRR receptor‐like protein associates with its adaptor kinase OsSOBIR1 to mediate plant immunity against viral infection

inferred← citeshttps://doi.org/10.1111/pce.12686openalex-snapshot

Functional characterization of the chaperon‐like protein Cdc48 in cryptogein‐induced immune response in tobacco

inferred← citeshttps://doi.org/10.1111/pce.13850openalex-snapshot

Physiological significance of pedospheric nitric oxide for root growth, development and organismic interactions

inferred← citeshttps://doi.org/10.1111/pce.15363openalex-snapshot

sly‐miR408b Targets a Plastocyanin‐Like Protein to Regulate Mycorrhizal Symbiosis in Tomato

inferred← citeshttps://doi.org/10.1126/scisignal.aad4403openalex-snapshot

Occurrence, structure, and evolution of nitric oxide synthase–like proteins in the plant kingdom

inferred← citeshttps://doi.org/10.1186/s12964-016-0133-2openalex-snapshot

The arabidopsis cyclic nucleotide interactome

inferred← citeshttps://doi.org/10.1371/journal.pone.0163546openalex-snapshot

Contrasting Regulation of NO and ROS in Potato Defense-Associated Metabolism in Response to Pathogens of Different Lifestyles

inferred← citeshttps://doi.org/10.15421/0226077openalex-snapshot

Synthesis of a kinetin and graphene oxide nanoensemble and its effects on defense responses of cotton against Verticillium dahliae

inferred← citeshttps://doi.org/10.15446/rfna.v70n2.64526openalex-snapshot

Plant responses to pathogen attack: molecular basis of qualitative resistance

inferred← citeshttps://doi.org/10.3389/fchem.2014.00114openalex-snapshot

Protein S-nitrosylation: specificity and identification strategies in plants

inferred← citeshttps://doi.org/10.3389/fpls.2015.00977openalex-snapshot

Plant Survival in a Changing Environment: The Role of Nitric Oxide in Plant Responses to Abiotic Stress

inferred← citeshttps://doi.org/10.3389/fpls.2022.887674openalex-snapshot

Not Only Systemin: Prosystemin Harbors Other Active Regions Able to Protect Tomato Plants

inferred← citeshttps://doi.org/10.3389/fpls.2022.952397openalex-snapshot

Development of plant systemic resistance by beneficial rhizobacteria: Recognition, initiation, elicitation and regulation

inferred← citeshttps://doi.org/10.3389/fpls.2023.1158184openalex-snapshot

Functions of nitric oxide-mediated post-translational modifications under abiotic stress

inferred← citeshttps://doi.org/10.3389/fpls.2026.1796014openalex-snapshot

Peroxynitrite-mediated tyrosine nitration modulates β-1,3-glucanase activity and potato defense against Phytophthora infestans

inferred← citeshttps://doi.org/10.3390/antiox10071128openalex-snapshot

GSNOR Contributes to Demethylation and Expression of Transposable Elements and Stress-Responsive Genes

inferred← citeshttps://doi.org/10.3390/antiox12071321openalex-snapshot

Nitric Oxide and Globin Glb1 Regulate Fusarium oxysporum Infection of Arabidopsis thaliana

inferred← citeshttps://doi.org/10.3390/horticulturae8050451openalex-snapshot

Application of Elicitors in Grapevine Defense: Impact on Volatile Compounds

inferred← citeshttps://doi.org/10.3390/ijms19113590openalex-snapshot

Role of Ca2+ in Mediating Plant Responses to Extracellular ATP and ADP

inferred← citeshttps://doi.org/10.3390/ijms20194881openalex-snapshot

Multilevel Regulation of Peroxisomal Proteome by Post-Translational Modifications

inferred← citeshttps://doi.org/10.3390/ijms21030963openalex-snapshot

Elicitor and Receptor Molecules: Orchestrators of Plant Defense and Immunity

inferred← citeshttps://doi.org/10.3390/ijms23074051openalex-snapshot

Nitric Oxide Implication in Potato Immunity to Phytophthora infestans via Modifications of Histone H3/H4 Methylation Patterns on Defense Genes

inferred← citeshttps://doi.org/10.3390/nitrogen1010003openalex-snapshot

Assessing Nitric Oxide (NO) in Higher Plants: An Outline

inferred← citeshttps://doi.org/10.3390/plants10071451openalex-snapshot

Protein Carbonylation: Emerging Roles in Plant Redox Biology and Future Prospects

inferred← citeshttps://doi.org/10.3390/plants14030344openalex-snapshot

Integrating Physiology, Transcriptome, and Metabolomics Reveals the Potential Mechanism of Nitric Oxide Concentration-Dependent Regulation of Embryo Germination in Sorbus pohuashanensis

inferred← citeshttps://doi.org/10.3390/plants8020037openalex-snapshot

Impact of Nitric Oxide (NO) on the ROS Metabolism of Peroxisomes

inferred← citeshttps://doi.org/10.70675/113dfdaaz2de4z41d6zbf96z59486ceff3c9openalex-snapshot

Etude du rôle de la protéine CDC48 dans l'immunité des plantes

inferred← citeshttps://doi.org/10.70675/12ba579az6091z4ef5zb308zdd7d15deb069openalex-snapshot

Identification et caractérisation des acteurs protéiques de la membrane plasmique impliqués dans la perception des rhamnolipides chez Arabidopsis thaliana

inferred← citeshttps://doi.org/10.70675/ec236e1bz74ccz4649z8b2ez1321333019f4openalex-snapshot

Induction de la PAMP-Triggered Immunity par des éliciteurs d’origine différente chez Solanum tuberosum

inferred← citeshttps://doi.org/10.70675/fa6f60bdzb6a5z41d8za5edz0913d0875eaeopenalex-snapshot

Identification du xyloglucane comme nouvel éliciteur oligosaccharidique stimulant l’immunité de Vitis vinifera et d’Arabidopsis thaliana et caractérisation de deux récepteurs aux chito-oligosaccharides chez la vigne (VvLYK1-1 et VvLYK1-2)

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