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The role of a cytosolic superoxide dismutase in barley–pathogen interactions
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Role of reactive oxygen species in the response of barley to necrotrophic pathogens
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Proteomic analysis reveals the potential involvement of xylanase from Pyrenophora teres f. teres in net form net blotch disease of barley
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Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels
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H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response
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The generation of oxygen radicals during host plant responses to infection
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International Review Of Cell and Molecular Biology
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BcGs1, a glycoprotein from Botrytis cinerea , elicits defence response and improves disease resistance in host plants
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Role of hydrogen peroxide and antioxidant enzymes in the interaction between a hemibiotrophic fungal pathogen, Leptosphaeria maculans, and oilseed rape
inferredcites →https://doi.org/10.1016/j.febslet.2011.10.048openalex-snapshot
Superoxide dismutases: Ancient enzymes and new insights
inferredcites →https://doi.org/10.1016/j.mib.2008.10.008openalex-snapshot
Role of reactive oxygen species in fungal cellular differentiations
inferredcites →https://doi.org/10.1016/j.mib.2012.10.002openalex-snapshot
Reactive oxygen species generation in fungal development and pathogenesis
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Reactive oxygen species and plant resistance to fungal pathogens
inferredcites →https://doi.org/10.1016/j.plaphy.2012.01.014openalex-snapshot
The Janus face of reactive oxygen species in resistance and susceptibility of plants to necrotrophic and biotrophic pathogens
inferredcites →https://doi.org/10.1016/j.pmpp.2008.05.003openalex-snapshot
Initial characterisation of phytotoxic proteins isolated from Pyrenophora teres
inferredcites →https://doi.org/10.1016/j.pmpp.2011.12.005openalex-snapshot
The CuZn superoxide dismutase from Sclerotinia sclerotiorum is involved with oxidative stress tolerance, virulence, and oxalate production
inferredcites →https://doi.org/10.1016/j.tplants.2004.08.009openalex-snapshot
Reactive oxygen gene network of plants
inferredcites →https://doi.org/10.1016/s0021-9258(19)42815-9openalex-snapshot
Univalent Reduction of Molecular Oxygen by Spinach Chloroplasts on Illumination
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Association of hydrogen peroxide with restriction of Septoria tritici in resistant wheat
inferredcites →https://doi.org/10.1016/s0960-9822(00)00560-1openalex-snapshot
The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea
inferredcites →https://doi.org/10.1016/s1937-6448(08)01403-2openalex-snapshot
Chapter 3: Programmed Cell Death in Plants
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Elevated Levels of Superoxide Dismutase Protect Transgenic Plants Against Ozone Damage
inferredcites →https://doi.org/10.1038/nchembio.164openalex-snapshot
Networking by small-molecule hormones in plant immunity
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Construct design for efficient, effective and high‐throughput gene silencing in plants
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Growth of Pyrenophora teres in planta during barley net blotch disease
inferredcites →https://doi.org/10.1071/fp08109openalex-snapshot
Identification and characterisation of barley (Hordeum vulgare) respiratory burst oxidase homologue family members
inferredcites →https://doi.org/10.1073/pnas.231178298openalex-snapshot
Signal interactions between nitric oxide and reactive oxygen intermediates in the plant hypersensitive disease resistance response
inferredcites →https://doi.org/10.1073/pnas.87.24.9903openalex-snapshot
Characterization of iron superoxide dismutase cDNAs from plants obtained by genetic complementation in Escherichia coli.
inferredcites →https://doi.org/10.1073/pnas.90.4.1629openalex-snapshot
Increased resistance to oxidative stress in transgenic plants that overexpress chloroplastic Cu/Zn superoxide dismutase.
inferredcites →https://doi.org/10.1080/07352689409701914openalex-snapshot
Superoxide Dismutase in Plants
inferredcites →https://doi.org/10.1089/ars.2013.5679openalex-snapshot
Redox Regulation in Plant Immune Function
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Antioxidants, Oxidative Damage and Oxygen Deprivation Stress: a Review
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Sclerotial metamorphosis in filamentous fungi is induced by oxidative stress
inferredcites →https://doi.org/10.1093/jexbot/53.372.1331openalex-snapshot
Role of superoxide dismutases (SODs) in controlling oxidative stress in plants
inferredcites →https://doi.org/10.1093/jxb/ert375openalex-snapshot
ROS as key players in plant stress signalling
inferredcites →https://doi.org/10.1093/jxb/erv154openalex-snapshot
Differential effects of lesion mimic mutants in barley on disease development by facultative pathogens
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029014openalex-snapshot
Intra- and Extra-Cellular Localization of "Cytosolic" CuZn-Superoxide Dismutase in Spinach Leaf and Hypocotyl
inferredcites →https://doi.org/10.1094/mpmi-20-2-0178openalex-snapshot
Transcriptional Adaptation of Mycosphaerella graminicola to Programmed Cell Death (PCD) of Its Susceptible Wheat Host
inferredcites →https://doi.org/10.1094/mpmi-21-9-1143openalex-snapshot
Leptosphaeria maculans Elicits Apoptosis Coincident with Leaf Lesion Formation and Hyphal Advance in Brassica napus
inferredcites →https://doi.org/10.1094/mpmi-22-8-0987openalex-snapshot
Does Botrytis cinerea Ignore H2O2-Induced Oxidative Stress During Infection? Characterization of Botrytis Activator Protein 1
inferredcites →https://doi.org/10.1094/mpmi-23-9-1143openalex-snapshot
RBOHF2 of Barley Is Required for Normal Development of Penetration Resistance to the Parasitic Fungus Blumeria graminis f. sp. hordei
inferredcites →https://doi.org/10.1094/mpmi-7-0401openalex-snapshot
The Relationship Between the Expression of Defense-Related Genes and Mildew Development in Barley
inferredcites →https://doi.org/10.1094/mpmi.1998.11.4.292openalex-snapshot
Tissue-Specific Superoxide Generation at Interaction Sites in Resistant and Susceptible Near-Isogenic Barley Lines Attacked by the Powdery Mildew Fungus (Erysiphe graminis f. sp. hordei)
inferredcites →https://doi.org/10.1094/mpmi.2004.17.1.27openalex-snapshot
Host Responses to Transient Expression of Individual Genes Encoded by Tomato leaf curl virus
inferredcites →https://doi.org/10.1094/phyto-05-13-0133-ropenalex-snapshot
Histochemical Characterization of Early Response to Cochliobolus sativus Infection in Selected Barley Genotypes
inferredcites →https://doi.org/10.1094/phyto-97-8-0907openalex-snapshot
Proteinaceous Metabolites from Pyrenophora teres Contribute to Symptom Development of Barley Net Blotch
inferredcites →https://doi.org/10.1094/phyto.2001.91.2.127openalex-snapshot
A Compromised Mlo Pathway Affects the Response of Barley to the Necrotrophic Fungus Bipolaris sorokiniana (Teleomorph: Cochliobolus sativus) and Its Toxins
inferredcites →https://doi.org/10.1104/pp.011021openalex-snapshot
Common Components, Networks, and Pathways of Cross-Tolerance to Stress. The Central Role of “Redox” and Abscisic Acid-Mediated Controls
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A Gateway Cloning Vector Set for High-Throughput Functional Analysis of Genes in Planta
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Mitochondrial Reactive Oxygen Species. Contribution to Oxidative Stress and Interorganellar Signaling
inferredcites →https://doi.org/10.1104/pp.109.1.203openalex-snapshot
Differential Accumulation of Antioxidant mRNAs in Arabidopsis thaliana Exposed to Ozone
inferredcites →https://doi.org/10.1104/pp.117.2.491openalex-snapshot
Use of a New Tetrazolium-Based Assay to Study the Production of Superoxide Radicals by Tobacco Cell Cultures Challenged with Avirulent Zoospores ofPhytophthora parasitica varnicotianae1
inferredcites →https://doi.org/10.1104/pp.118.2.637openalex-snapshot
Superoxide Dismutase in Arabidopsis: An Eclectic Enzyme Family with Disparate Regulation and Protein Localization
inferredcites →https://doi.org/10.1104/pp.119.4.1251openalex-snapshot
Hypersensitive Cell Death and Papilla Formation in Barley Attacked by the Powdery Mildew Fungus Are Associated with Hydrogen Peroxide but Not with Salicylic Acid Accumulation1
inferredcites →https://doi.org/10.1104/pp.124.2.899openalex-snapshot
Hydrogen Peroxide Yields during the Incompatible Interaction of Tobacco Suspension Cells Inoculated with Phytophthora nicotianae
inferredcites →https://doi.org/10.1105/tpc.108.061341openalex-snapshot
A Heterocomplex of Iron Superoxide Dismutases Defends Chloroplast Nucleoids against Oxidative Stress and Is Essential for Chloroplast Development inArabidopsis
inferredcites →https://doi.org/10.1111/j.1364-3703.2005.00304.xopenalex-snapshot
Metabolic and stress adaptation by Mycosphaerella graminicola during sporulation in its host revealed through microarray transcription profiling
inferredcites →https://doi.org/10.1111/j.1364-3703.2008.00475.xopenalex-snapshot
The Fusarium mycotoxin deoxynivalenol elicits hydrogen peroxide production, programmed cell death and defence responses in wheat
inferredcites →https://doi.org/10.1111/j.1364-3703.2008.00485.xopenalex-snapshot
Expression profiling and mapping of defence response genes associated with the barley– Pyrenophora teres incompatible interaction
inferredcites →https://doi.org/10.1111/j.1365-3180.1974.tb01084.xopenalex-snapshot
A decimal code for the growth stages of cereals
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02026.xopenalex-snapshot
Role of hydrogen peroxide during the interaction between the hemibiotrophic fungal pathogen Septoria tritici and wheat
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02970.xopenalex-snapshot
Wheat blast: histopathology and transcriptome reprogramming in response to adapted and nonadapted Magnaporthe isolates
inferredcites →https://doi.org/10.1111/mpp.12172openalex-snapshot
Necrotrophic effector‐triggered susceptibility ( NETS ) underlies the barley– P yrenophora teres f. teres interaction specific to chromosome 6H
inferredcites →https://doi.org/10.1111/mpp.12173openalex-snapshot
Contribution of the drought tolerance‐related Stress‐responsive NAC 1 transcription factor to resistance of barley to R amularia leaf spot
inferredcites →https://doi.org/10.1111/nph.12530openalex-snapshot
Robust anti‐oxidant defences in the rice blast fungusMagnaporthe oryzaeconfer tolerance to the host oxidative burst
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-114623openalex-snapshot
Fungal Effectors and Plant Susceptibility
inferredcites →https://doi.org/10.1146/annurev-phyto-072910-095355openalex-snapshot
Reactive Oxygen Species in Phytopathogenic Fungi: Signaling, Development, and Disease
inferredcites →https://doi.org/10.1146/annurev.bi.44.070175.001051openalex-snapshot
Superoxide Dismutases
inferredcites →https://doi.org/10.1155/2012/514398openalex-snapshot
Poor Homologous Synapsis 1 Interacts with Chromatin but Does Not Colocalise with ASYnapsis 1 during Early Meiosis in Bread Wheat
inferredcites →https://doi.org/10.1186/1471-2229-10-146openalex-snapshot
Validation of reference genes as internal control for studying viral infections in cereals by quantitative real-time RT-PCR
inferredcites →https://doi.org/10.1186/1471-2229-10-9openalex-snapshot
Differential gene expression in incompatible interaction between wheat and stripe rust fungus revealed by cDNA-AFLP and comparison to compatible interaction
inferredcites →https://doi.org/10.1186/1471-2229-7-67openalex-snapshot
TaMSH7: A cereal mismatch repair gene that affects fertility in transgenic barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1371/journal.pone.0019008openalex-snapshot
Resistance to Hemi-Biotrophic F. graminearum Infection Is Associated with Coordinated and Ordered Expression of Diverse Defense Signaling Pathways
inferredcites →https://doi.org/10.1534/genetics.113.159368openalex-snapshot
New Insights Into the Roles of NADPH Oxidases in Sexual Development and Ascospore Germination in Sordaria macrospora
inferredcites →https://doi.org/10.1556/aphyt.38.2003.3-4.2openalex-snapshot
Role of Hydrogen Peroxide in Symptom Expression of Barley Susceptible and Resistant to Powdery Mildew
inferredcites →https://doi.org/10.3186/jjphytopath.49.270openalex-snapshot
Time-course alteration of lipid peroxidation and the activities of superoxide dismutase, catalase and peroxidase in blast-infected rice leaves.
inferredcites →https://doi.org/10.3389/fpls.2013.00419openalex-snapshot
Nitric oxide, antioxidants and prooxidants in plant defence responses
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Suppression of plant-generated reactive oxygen species is required for successful infection by the rice blast fungus
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Differential Regulation of Superoxide Dismutase Activity in Selected Strawberry Lines Exposed to Mycosphaerella fragariae
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.3390/su14052597openalex-snapshot
The Stimulation of Superoxide Dismutase Enzyme Activity and Its Relation with the Pyrenophora teres f. teres Infection in Different Barley Genotypes
inferred← citeshttps://doi.org/10.5423/ppj.oa.09.2018.0180openalex-snapshot
Hydrogen Peroxide Prompted Lignification Affects Pathogenicity of Hemi-biotrophic Pathogen Bipolaris sorokiniana to Wheat
inferred← citeshttps://doi.org/10.55905/rdelosv16.n43-006openalex-snapshot
Antioxidant enzyme activity associated to Meloidogyne and Pratylenchus infection in sugarcane
inferred← citeshttps://doi.org/10.55905/rdelosv16.n44-021openalex-snapshot
Respostas enzimáticas da cana-de-açúcar em área de sequeiro
inferred← citeshttps://doi.org/10.6084/m9.figshare.14368860openalex-snapshot
Additional file 1 of Label-free quantitative proteomics of Sorghum bicolor reveals the proteins strengthening plant defense against insect pest Chilo partellus
inferred← citeshttps://doi.org/10.6084/m9.figshare.14368863openalex-snapshot
Additional file 2 of Label-free quantitative proteomics of Sorghum bicolor reveals the proteins strengthening plant defense against insect pest Chilo partellus
inferred← citeshttps://doi.org/10.70675/c7c88209z76a0z4526zb385z102b8a4dc49copenalex-snapshot
Lutte BiHO : Lutte Biologique contre l’Helminthosporiose de l’Orge
inferred← citeshttps://doi.org/10.70675/cb94ddbbz90abz4a78z8a86z0cf479e24812openalex-snapshot
Caractérisation biochimique et structurale de quelques glutathion transférases de la classe Tau d'arabette (Arabidopsis thaliana) et de peuplier (Populus trichocarpa)
inferred← citeshttps://doi.org/10.7287/peerj.15392v0.1/reviews/1openalex-snapshot
Peer Review #1 of "New seed coating containing Trichoderma viride with anti-pathogenic properties (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15392v0.1/reviews/2openalex-snapshot
Peer Review #2 of "New seed coating containing Trichoderma viride with anti-pathogenic properties (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15392v0.2/reviews/1openalex-snapshot
Peer Review #1 of "New seed coating containing Trichoderma viride with anti-pathogenic properties (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.15392v0.2/reviews/2openalex-snapshot
Peer Review #2 of "New seed coating containing Trichoderma viride with anti-pathogenic properties (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.15392openalex-snapshot
New seed coating containing Trichoderma viride with anti-pathogenic properties
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.