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Of PAMPs and Effectors: The Blurred PTI-ETI Dichotomy
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1 of the 135 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1126/science.1173438 (notice 2013-10-11).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbic.200700693openalex-snapshot
The Acylation and Phosphorylation Pattern of Lipid A from Xanthomonas Campestris Strongly Influence its Ability to Trigger the Innate Immune Response in Arabidopsis
inferredcites →https://doi.org/10.1006/pmpp.1995.1004openalex-snapshot
The phytopathogenic fungus Cladosporium fulvum is not sensitive to the chitinase and β-1,3-glucanase defence proteins of its host, tomato
inferredcites →https://doi.org/10.1006/pmpp.1995.1048openalex-snapshot
The role of the coating response in Craigella tomatoes infected with Verticillium dahliae, races 1 and 2
inferredcites →https://doi.org/10.1006/pmpp.1998.0163openalex-snapshot
Cyclical systemic colonization inVerticillium-infected tomato
inferredcites →https://doi.org/10.1007/s004250000325openalex-snapshot
Identification of high-affinity binding sites for the hepta-β-glucoside elicitor in membranes of the model legumes Medicago truncatula and Lotus japonicus
inferredcites →https://doi.org/10.1007/s004380051148openalex-snapshot
The Cf-ECP2 gene is linked to, but not part of, the Cf-4/Cf-9 cluster on the short arm of chromosome 1 in tomato
inferredcites →https://doi.org/10.1007/s10327-005-0201-8openalex-snapshot
Defense responses of Arabidopsis thaliana inoculated with Pseudomonas syringae pv. tabaci wild type and defective mutants for flagellin (ΔfliC) and flagellin-glycosylation (Δorf1)
inferredcites →https://doi.org/10.1007/s10327-007-0017-9openalex-snapshot
N-terminal domain including conserved flg22 is required for flagellin-induced hypersensitive cell death in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11103-007-9173-8openalex-snapshot
Molecular identification and characterization of the tomato flagellin receptor LeFLS2, an orthologue of Arabidopsis FLS2 exhibiting characteristically different perception specificities
inferredcites →https://doi.org/10.1016/0092-8674(94)90423-5openalex-snapshot
High affinity binding of a fungal oligopeptide elicitor to parsley plasma membranes triggers multiple defense responses
inferredcites →https://doi.org/10.1016/0092-8674(95)90515-4openalex-snapshot
Ectopic expression of the flagellar regulon alters development of the bordetella-host interaction
inferredcites →https://doi.org/10.1016/j.cell.2006.02.008openalex-snapshot
Host-Microbe Interactions: Shaping the Evolution of the Plant Immune Response
inferredcites →https://doi.org/10.1016/j.cell.2006.03.037openalex-snapshot
Perception of the Bacterial PAMP EF-Tu by the Receptor EFR Restricts Agrobacterium-Mediated Transformation
inferredcites →https://doi.org/10.1016/j.cell.2009.02.036openalex-snapshot
Autophagic Components Contribute to Hypersensitive Cell Death in Arabidopsis
inferredcites →https://doi.org/10.1016/j.chembiol.2008.03.017openalex-snapshot
Peptidoglycan and Muropeptides from Pathogens Agrobacterium and Xanthomonas Elicit Plant Innate Immunity: Structure and Activity
inferredcites →https://doi.org/10.1016/j.copbio.2010.02.004openalex-snapshot
Biotechnological concepts for improving plant innate immunity
inferredcites →https://doi.org/10.1016/j.cub.2007.05.046openalex-snapshot
The BRI1-Associated Kinase 1, BAK1, Has a Brassinolide-Independent Role in Plant Cell-Death Control
inferredcites →https://doi.org/10.1016/j.cub.2007.10.042openalex-snapshot
Nuclear Accumulation of the Arabidopsis Immune Receptor RPS4 Is Necessary for Triggering EDS1-Dependent Defense
inferredcites →https://doi.org/10.1016/j.cub.2008.06.061openalex-snapshot
Bacterial Polysaccharides Suppress Induced Innate Immunity by Calcium Chelation
inferredcites →https://doi.org/10.1016/j.pbi.2010.04.006openalex-snapshot
Comparing signaling mechanisms engaged in pattern-triggered and effector-triggered immunity
inferredcites →https://doi.org/10.1016/j.pbi.2010.04.012openalex-snapshot
Recent advances in rice blast effector research
inferredcites →https://doi.org/10.1016/j.phytochem.2005.12.008openalex-snapshot
Nep1-like proteins from plant pathogens: Recruitment and diversification of the NPP1 domain across taxa
inferredcites →https://doi.org/10.1016/j.pmpp.2004.10.002openalex-snapshot
Tolerance to a non-host isolate of Verticillium dahliae in tomato
inferredcites →https://doi.org/10.1016/j.pmpp.2005.06.001openalex-snapshot
Motility is an important determinant for pathogenesis of Erwinia carotovora subsp. carotovora
inferredcites →https://doi.org/10.1016/j.tim.2009.01.002openalex-snapshot
Fungal LysM effectors: extinguishers of host immunity?
inferredcites →https://doi.org/10.1016/s0074-7696(08)62404-3openalex-snapshot
Elicitors of Plant Defense Responses
inferredcites →https://doi.org/10.1016/s0092-8674(00)80412-2openalex-snapshot
Innate Immunity: The Virtues of a Nonclonal System of Recognition
inferredcites →https://doi.org/10.1016/s0092-8674(00)81092-2openalex-snapshot
Active and Inactive Protein Kinases: Structural Basis for Regulation
inferredcites →https://doi.org/10.1016/s0968-0004(98)01311-5openalex-snapshot
Plant disease-resistance proteins and the gene-for-gene concept
inferredcites →https://doi.org/10.1016/s1369-5266(02)00265-0openalex-snapshot
Innate immunity in plants and animals: emerging parallels between the recognition of general elicitors and pathogen-associated molecular patterns
inferredcites →https://doi.org/10.1038/367384a0openalex-snapshot
Host resistance to a fungal tomato pathogen lost by a single base-pair change in an avirulence gene
inferredcites →https://doi.org/10.1038/nature02485openalex-snapshot
Bacterial disease resistance in Arabidopsis through flagellin perception
inferredcites →https://doi.org/10.1038/nature05999openalex-snapshot
A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence
inferredcites →https://doi.org/10.1038/nature08358openalex-snapshot
Genome sequence and analysis of the Irish potato famine pathogen Phytophthora infestans
inferredcites →https://doi.org/10.1038/nbt.1613openalex-snapshot
Interfamily transfer of a plant pattern-recognition receptor confers broad-spectrum bacterial resistance
inferredcites →https://doi.org/10.1038/ni0107-11openalex-snapshot
Friendly and dangerous signals: is the tissue in control?
inferredcites →https://doi.org/10.1038/ni1386openalex-snapshot
Virulence factors of Yersinia pestis are overcome by a strong lipopolysaccharide response
inferredcites →https://doi.org/10.1038/nrg2812openalex-snapshot
Plant immunity: towards an integrated view of plant–pathogen interactions
inferredcites →https://doi.org/10.1046/j.1365-313x.1993.04020307.xopenalex-snapshot
Specific perception of subnanomolar concentrations of chitin fragments by tomato cells: induction of extracellular alkalinization, changes in protein phosphorylation, and establishment of a refractory state
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00265.xopenalex-snapshot
Plants have a sensitive perception system for the most conserved domain of bacterial flagellin
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00843.xopenalex-snapshot
Specific HR‐associated recognition of secreted proteins from Cladosporium fulvum occurs in both host and non‐host plants
inferredcites →https://doi.org/10.1073/pnas.011265298openalex-snapshot
HrpZPsph from the plant pathogen Pseudomonas syringae pv. phaseolicola binds to lipid bilayers and forms an ion-conducting pore invitro
inferredcites →https://doi.org/10.1073/pnas.0307553101openalex-snapshot
Pseudomonas aeruginosa regulates flagellin expression as part of a global response to airway fluid from cystic fibrosis patients
inferredcites →https://doi.org/10.1073/pnas.0404536101openalex-snapshot
Innate immunity in Arabidopsis thaliana : Lipopolysaccharides activate nitric oxide synthase (NOS) and induce defense genes
inferredcites →https://doi.org/10.1073/pnas.0508882103openalex-snapshot
Plant cells recognize chitin fragments for defense signaling through a plasma membrane receptor
inferredcites →https://doi.org/10.1073/pnas.0605508103openalex-snapshot
Unique characteristics of Xanthomonas oryzae pv. oryzae AvrXa21 and implications for plant innate immunity
inferredcites →https://doi.org/10.1073/pnas.0705147104openalex-snapshot
CERK1, a LysM receptor kinase, is essential for chitin elicitor signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0705306104openalex-snapshot
The receptor-like kinase SERK3/BAK1 is a central regulator of innate immunity in plants
inferredcites →https://doi.org/10.1073/pnas.1002910107openalex-snapshot
Tomato Cf resistance proteins mediate recognition of cognate homologous effectors from fungi pathogenic on dicots and monocots
inferredcites →https://doi.org/10.1073/pnas.1431173100openalex-snapshot
A Pseudomonas syringae type III effector suppresses cell wall-based extracellular defense in susceptible Arabidopsis plants
inferredcites →https://doi.org/10.1073/pnas.95.15.9014openalex-snapshot
Successful search for a resistance gene in tomato targeted against a virulence factor of a fungal pathogen
inferredcites →https://doi.org/10.1074/jbc.m004796200openalex-snapshot
Flagellin from an Incompatible Strain of Pseudomonas avenae Induces a Resistance Response in Cultured Rice Cells
inferredcites →https://doi.org/10.1074/jbc.m109.027540openalex-snapshot
Direct Binding of a Plant LysM Receptor-like Kinase, LysM RLK1/CERK1, to Chitin in Vitro
inferredcites →https://doi.org/10.1074/jbc.m110.116657openalex-snapshot
The Lysin Motif Receptor-like Kinase (LysM-RLK) CERK1 Is a Major Chitin-binding Protein in Arabidopsis thaliana and Subject to Chitin-induced Phosphorylation
inferredcites →https://doi.org/10.1074/jbc.m209880200openalex-snapshot
Molecular Sensing of Bacteria in Plants
inferredcites →https://doi.org/10.1074/jbc.m212196200openalex-snapshot
Natural Disulfide Bond-disrupted Mutants of AVR4 of the Tomato Pathogen Cladosporium fulvum Are Sensitive to Proteolysis, Circumvent Cf-4-mediated Resistance, but Retain Their Chitin Binding Ability
inferredcites →https://doi.org/10.1074/jbc.m312594200openalex-snapshot
Binding of the AVR4 Elicitor of Cladosporium fulvum to Chitotriose Units Is Facilitated by Positive Allosteric Protein-Protein Interactions
inferredcites →https://doi.org/10.1074/jbc.m704886200openalex-snapshot
Bacteria-derived Peptidoglycans Constitute Pathogen-associated Molecular Patterns Triggering Innate Immunity in Arabidopsis
inferredcites →https://doi.org/10.1080/07352689.2010.502082openalex-snapshot
The Diverse Roles of Extracellular Leucine-rich Repeat-containing Receptor-like Proteins in Plants
inferredcites →https://doi.org/10.1093/emboj/cdf667openalex-snapshot
Pep‐13, a plant defense‐inducing pathogen‐associated pattern from Phytophthora transglutaminases
inferredcites →https://doi.org/10.1093/pcp/pcg042openalex-snapshot
Post-Translational Modification of Flagellin Determines the Specificity of HR Induction
inferredcites →https://doi.org/10.1094/mpmi-19-1420openalex-snapshot
Cladosporium fulvum Avr4 Protects Fungal Cell Walls Against Hydrolysis by Plant Chitinases Accumulating During Infection
inferredcites →https://doi.org/10.1094/mpmi-20-10-1271openalex-snapshot
Allelic Variation in the Effector Genes of the Tomato Pathogen Cladosporium fulvum Reveals Different Modes of Adaptive Evolution
inferredcites →https://doi.org/10.1094/mpmi-20-9-1092openalex-snapshot
The Chitin-Binding Cladosporium fulvum Effector Protein Avr4 Is a Virulence Factor
inferredcites →https://doi.org/10.1094/mpmi-21-12-1635openalex-snapshot
Analysis of Flagellin Perception Mediated by flg22 Receptor OsFLS2 in Rice
inferredcites →https://doi.org/10.1094/mpmi-21-9-1165openalex-snapshot
Amino Acid Sequence of Bacterial Microbe-Associated Molecular Pattern flg22 Is Required for Virulence
inferredcites →https://doi.org/10.1094/mpmi-22-3-0245openalex-snapshot
Tomato Transcriptional Responses to a Foliar and a Vascular Fungal Pathogen Are Distinct
inferredcites →https://doi.org/10.1094/mpmi-8-0939openalex-snapshot
ThePWLHost Specificity Gene Family in the Blast FungusMagnaporthe grisea
inferredcites →https://doi.org/10.1094/mpmi.1997.10.6.725openalex-snapshot
The In Planta-Produced Extracellular Proteins ECP1 and ECP2 of Cladosporium fulvum Are Virulence Factors
inferredcites →https://doi.org/10.1094/mpmi.1997.10.9.1045openalex-snapshot
Cloning and Characterization of a cDNA Encoding an Elicitor of Phytophthora parasitica var. nicotianae That Shows Cellulose-Binding and Lectin-Like Activities
inferredcites →https://doi.org/10.1094/mpmi.2004.17.6.593openalex-snapshot
Bacterial Genes Involved in Type I Secretion and Sulfation Are Required to Elicit the Rice Xa21-Mediated Innate Immune Response
inferredcites →https://doi.org/10.1094/mpmi.2004.17.6.686openalex-snapshot
Swimming Motility, a Virulence Trait of Ralstonia solanacearum, Is Regulated by FlhDC and the Plant Host Environment
inferredcites →https://doi.org/10.1094/mpmi.2004.17.6.696openalex-snapshot
Flagellin Is Not a Major Defense Elicitor in Ralstonia solanacearum Cells or Extracts Applied to Arabidopsis thaliana
inferredcites →https://doi.org/10.1094/phyto-64-1389openalex-snapshot
Role of Flagellar Motility in the Invasion of Bean Leaves by Pseudomonas phaseolicola
inferredcites →https://doi.org/10.1094/phyto-79-284openalex-snapshot
Motility ofPseudomonas syringaepv.glycineaand its Role in Infection
inferredcites →https://doi.org/10.1099/mic.0.030700-0openalex-snapshot
Defects in flagellin glycosylation affect the virulence of Pseudomonas syringae pv. tabaci 6605
inferredcites →https://doi.org/10.1101/gr.910003openalex-snapshot
EST Mining and Functional Expression Assays Identify Extracellular Effector Proteins From the Plant PathogenPhytophthora
inferredcites →https://doi.org/10.1104/pp.106.090985openalex-snapshot
The Lipopolysaccharide of Sinorhizobium meliloti Suppresses Defense-Associated Gene Expression in Cell Cultures of the Host Plant Medicago truncatula
inferredcites →https://doi.org/10.1104/pp.108.119487openalex-snapshot
A Genome-Wide Functional Investigation into the Roles of Receptor-Like Proteins in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.136762openalex-snapshot
Genetic Dissection ofVerticilliumWilt Resistance Mediated by Tomato Ve1
inferredcites →https://doi.org/10.1104/pp.124.3.1027openalex-snapshot
Linear β-1,3 Glucans Are Elicitors of Defense Responses in Tobacco
inferredcites →https://doi.org/10.1104/pp.94.4.1849openalex-snapshot
An Ethylene Biosynthesis-Inducing Endoxylanase Elicits Electrolyte Leakage and Necrosis in Nicotiana tabacum cv Xanthi Leaves
inferredcites →https://doi.org/10.1105/tpc.007591openalex-snapshot
Quantitative Nature of Arabidopsis Responses during Compatible and Incompatible Interactions with the Bacterial PathogenPseudomonas syringae [W]
inferredcites →https://doi.org/10.1105/tpc.022475openalex-snapshot
The Receptor for the Fungal Elicitor Ethylene-Inducing Xylanase Is a Member of a Resistance-Like Gene Family in Tomato
inferredcites →https://doi.org/10.1105/tpc.105.036574openalex-snapshot
The Arabidopsis Receptor Kinase FLS2 Binds flg22 and Determines the Specificity of Flagellin Perception
inferredcites →https://doi.org/10.1105/tpc.105.037648openalex-snapshot
Within-Species Flagellin Polymorphism inXanthomonas campestrispvcampestrisand Its Impact on Elicitation ofArabidopsis FLAGELLIN SENSING2–Dependent Defenses
inferredcites →https://doi.org/10.1105/tpc.107.056325openalex-snapshot
Fungal Effector Protein AVR2 Targets Diversifying Defense-Related Cys Proteases of Tomato
inferredcites →https://doi.org/10.1105/tpc.107.056754openalex-snapshot
A LysM Receptor-Like Kinase Plays a Critical Role in Chitin Signaling and Fungal Resistance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.059394openalex-snapshot
TheCladosporium fulvumVirulence Protein Avr2 Inhibits Host Proteases Required for Basal Defense
inferredcites →https://doi.org/10.1105/tpc.109.069666openalex-snapshot
Translocation of Magnaporthe oryzae Effectors into Rice Cells and Their Subsequent Cell-to-Cell Movement
inferredcites →https://doi.org/10.1105/tpc.11.5.781openalex-snapshot
The Rx Gene from Potato Controls Separate Virus Resistance and Cell Death Responses
inferredcites →https://doi.org/10.1105/tpc.12.5.817openalex-snapshot
Differences in the Recognition of Glucan Elicitor Signals between Rice and Soybean: β-Glucan Fragments from the Rice Blast Disease Fungus Pyricularia oryzae That Elicit Phytoalexin Biosynthesis in Suspension-Cultured Rice Cells
inferredcites →https://doi.org/10.1105/tpc.7.8.1221openalex-snapshot
Identification, cloning, and characterization of PWL2, a gene for host species specificity in the rice blast fungus.
inferredcites →https://doi.org/10.1105/tpc.8.2.251openalex-snapshot
Interference between Two Specific Pathogen Recognition Events Mediated by Distinct Plant Disease Resistance Genes.
inferredcites →https://doi.org/10.1105/tpc.9.3.367openalex-snapshot
The biotrophic fungus Cladosporium fulvum circumvents Cf-4-mediated resistance by producing unstable AVR4 elicitors.
inferredcites →https://doi.org/10.1111/j.1364-3703.2004.00239.xopenalex-snapshot
Recognition of Cladosporium fulvum Ecp2 elicitor by non‐host Nicotiana spp. is mediated by a single dominant gene that is not homologous to known Cf ‐genes
inferredcites →https://doi.org/10.1111/j.1364-3703.2005.00292.xopenalex-snapshot
Cladosporium fulvum (syn. Passalora fulva ), a highly specialized plant pathogen as a model for functional studies on plant pathogenic Mycosphaerellaceae
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06270.xopenalex-snapshot
The novel Cladosporium fulvum lysin motif effector Ecp6 is a virulence factor with orthologues in other fungal species
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02981.xopenalex-snapshot
Early events in the pathogenicity of Pseudomonas syringae on Nicotiana benthamiana
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03067.xopenalex-snapshot
Pathogen‐associated molecular pattern recognition rather than development of tissue necrosis contributes to bacterial induction of systemic acquired resistance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03723.xopenalex-snapshot
Separable roles of the Pseudomonas syringae pv. phaseolicola accessory protein HrpZ1 in ion‐conducting pore formation and activation of plant immunity
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04324.xopenalex-snapshot
Two LysM receptor molecules, CEBiP and OsCERK1, cooperatively regulate chitin elicitor signaling in rice
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00672.xopenalex-snapshot
Porphyromonas gingivalis lipopolysaccharide lipid A heterogeneity: differential activities of tetra- and penta-acylated lipid A structures on E-selectin expression and TLR4 recognition
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00674.xopenalex-snapshot
Identification of glycosylation genes and glycosylated amino acids of flagellin in Pseudomonas syringae pv. tabaci
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00859.xopenalex-snapshot
Antagonistic lipopolysaccharides blockE. colilipopolysaccharide function at human TLR4 via interaction with the human MD-2 lipopolysaccharide binding site
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01043.xopenalex-snapshot
The CBEL elicitor of Phytophthora parasitica var. nicotianae activates defence in Arabidopsis thaliana via three different signalling pathways
inferredcites →https://doi.org/10.1111/j.1600-065x.2007.00579.xopenalex-snapshot
The grateful dead: damage‐associated molecular pattern molecules and reduction/oxidation regulate immunity
inferredcites →https://doi.org/10.1126/science.1071059openalex-snapshot
The Danger Model: A Renewed Sense of Self
inferredcites →https://doi.org/10.1126/science.1111404openalex-snapshot
Cladosporium Avr2 Inhibits Tomato Rcr3 Protease Required for Cf-2 -Dependent Disease Resistance
inferredcites →https://doi.org/10.1126/science.1173438openalex-snapshot
A Type I–Secreted, Sulfated Peptide Triggers XA21-Mediated Innate Immunity
inferredcites →https://doi.org/10.1126/science.1189468openalex-snapshot
Plant and Animal Sensors of Conserved Microbial Signatures
inferredcites →https://doi.org/10.1126/science.1190859openalex-snapshot
Conserved Fungal LysM Effector Ecp6 Prevents Chitin-Triggered Immunity in Plants
inferredcites →https://doi.org/10.1126/science.1621099openalex-snapshot
Harpin, Elicitor of the Hypersensitive Response Produced by the Plant Pathogen Erwinia amylovora
inferredcites →https://doi.org/10.1126/science.270.5243.1804openalex-snapshot
A Receptor Kinase-Like Protein Encoded by the Rice Disease Resistance Gene, Xa21
inferredcites →https://doi.org/10.1128/aem.53.10.2528-2533.1987openalex-snapshot
Flagellar Motility Confers Epiphytic Fitness Advantages upon Pseudomonas syringae
inferredcites →https://doi.org/10.1128/jb.01146-07openalex-snapshot
Identification of Harpins in Pseudomonas syringae pv. tomato DC3000, Which Are Functionally Similar to HrpK1 in Promoting Translocation of Type III Secretion System Effectors
inferredcites →https://doi.org/10.1128/jb.188.4.1381-1388.2006openalex-snapshot
Characterization of Late Acyltransferase Genes ofYersinia pestisand Their Role in Temperature-Dependent Lipid A Variation
inferredcites →https://doi.org/10.1146/annurev-phyto-073009-114407openalex-snapshot
Playing the “Harp”: Evolution of Our Understanding of hrp/hrc Genes
inferredcites →https://doi.org/10.1146/annurev.arplant.46.1.189openalex-snapshot
Chemoperception of Microbial Signals in Plant Cells
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105346openalex-snapshot
A Renaissance of Elicitors: Perception of Microbe-Associated Molecular Patterns and Danger Signals by Pattern-Recognition Receptors
inferredcites →https://doi.org/10.1146/annurev.ge.24.120190.002311openalex-snapshot
GENE-FOR-GENE COMPLEMENTARITY IN PLANT-PATHOGEN INTERACTIONS
inferredcites →https://doi.org/10.1146/annurev.phyto.38.1.241openalex-snapshot
The Induction and Modulation of Plant Defense Responses by Bacterial Lipopolysaccharides
inferredcites →https://doi.org/10.1146/annurev.phyto.44.070505.143436openalex-snapshot
A Catalogue of the Effector Secretome of Plant Pathogenic Oomycetes
inferredcites →https://doi.org/10.1146/annurev.phyto.45.062806.094427openalex-snapshot
Elicitors, Effectors, and R Genes: The New Paradigm and a Lifetime Supply of Questions
inferredcites →https://doi.org/10.1177/0968051907079399openalex-snapshot
Invited review: Priming, induction and modulation of plant defence responses by bacterial lipopolysaccharides
inferredcites →https://doi.org/10.1242/jcs.00138openalex-snapshot
The CBEL glycoprotein ofPhytophthora parasiticavar-nicotianaeis involved in cell wall deposition and adhesion to cellulosic substrates
inferredcites →https://doi.org/10.1371/journal.pgen.1000772openalex-snapshot
Network Properties of Robust Immunity in Plants
inferredcites →https://doi.org/10.1371/journal.ppat.0020002openalex-snapshot
Plant and Animal Pathogen Recognition Receptors Signal through Non-RD Kinases
inferredcites →https://doi.org/10.1371/journal.ppat.0020030openalex-snapshot
The MogR Transcriptional Repressor Regulates Nonhierarchal Expression of Flagellar Motility Genes and Virulence in Listeria monocytogenes
inferredcites →https://doi.org/10.1371/journal.ppat.1000388openalex-snapshot
Deletions in the Repertoire of Pseudomonas syringae pv. tomato DC3000 Type III Secretion Effector Genes Reveal Functional Overlap among Effectors
inferredcites →https://doi.org/10.1534/genetics.104.028985openalex-snapshot
Rearrangements in the Cf-9 Disease Resistance Gene Cluster of Wild Tomato Have Resulted in Three Genes That Mediate Avr9 ResponsivenessSequence data from this article have been deposited with the GenBank Data Libraries under accession no. AY569331.
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.4656134openalex-extracted
Overexpression of GmSRC2 Confers Resistance to Phytophthora Sojae in Soybean
inferred← citeshttps://doi.org/10.1002/9780470015902.a0003438.pub3openalex-snapshot
Plant Defences against Fungal Attack: Perception and Signal Transduction
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020103.pub2openalex-snapshot
Hypersensitive Response in Plants
inferred← citeshttps://doi.org/10.1002/9780470015902.a0023725openalex-snapshot
Recognition and Response in Plant PAMP ‐Triggered Immunity
inferred← citeshttps://doi.org/10.1002/9780470015902.a0023736openalex-snapshot
Posttranslational Modifications in Plant Disease Resistance
inferred← citeshttps://doi.org/10.1002/9781118382806.ch16openalex-snapshot
Behavioral and Molecular‐Genetic Basis of Resistance against Phloem‐Feeding Insects
inferred← citeshttps://doi.org/10.1002/9781118481431.ch10openalex-snapshot
Cladosporium fulvum –Tomato Pathosystem: Fungal Infection Strategy and Plant Responses
inferred← citeshttps://doi.org/10.1002/9781118481431.ch2openalex-snapshot
Molecular Basis of Effector Recognition by Plant NB‐LRR Proteins
inferred← citeshttps://doi.org/10.1002/9781118481431.ch7openalex-snapshot
Effectors of Fungi and Oomycetes: Their Virulence and Avirulence Functions and Translocation From Pathogen to Host Cells
inferred← citeshttps://doi.org/10.1002/9781118728475.ch2openalex-snapshot
Bacterial Blight Resistance in Rice
inferred← citeshttps://doi.org/10.1002/9781118829783.ch2openalex-snapshot
Herbivore Oral Secretions are the First Line of Protection Against Plant‐Induced Defences
inferred← citeshttps://doi.org/10.1002/9781118867716.ch12openalex-snapshot
Biotechnological Approaches for Crop Protection
inferred← citeshttps://doi.org/10.1002/9781118867716.ch2openalex-snapshot
Engineering Barriers to Infection by Undermining Pathogen Effector Function or by Gaining Effector Recognition
inferred← citeshttps://doi.org/10.1002/9781118958308.ch19openalex-snapshot
Secreted biomolecules in fungal plant pathogenesis
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0506openalex-snapshot
Herbivore Oral Secretions are the First Line of Protection Against Plant‐induced Defences
inferred← citeshttps://doi.org/10.1002/bies.201300155openalex-snapshot
Sex or no sex: Evolutionary adaptation occurs regardless
inferred← citeshttps://doi.org/10.1002/bies.201600101openalex-snapshot
A Pseudomonas aeruginosa‐secreted protease modulates host intrinsic immune responses, but how?
inferred← citeshttps://doi.org/10.1002/jobm.70112openalex-snapshot
Endophytes and Plants Interaction: A Hidden Microbial World Inside the Plant
inferred← citeshttps://doi.org/10.1002/mbo3.837openalex-snapshot
Targeting microbial pathogens by expression of new recombinant dermaseptin peptides in tobacco
inferred← citeshttps://doi.org/10.1002/pmic.201200402openalex-snapshot
Quantitative proteomics of tomato defense against Pseudomonas syringae infection
inferred← citeshttps://doi.org/10.1002/pmic.201300125openalex-snapshot
Protein interactome analysis of 12 mitogen‐activated protein kinase kinase kinase in rice using a yeast two‐hybrid system
inferred← citeshttps://doi.org/10.1002/pmic.201400463openalex-snapshot
Sugarcane proteomics: An update on current status, challenges, and future prospects
inferred← citeshttps://doi.org/10.1002/ps.8824openalex-snapshot
Enhancing plant resistance to tobacco mosaic virus through the combined application of Verticillium dahliae Aspf2‐like protein and microelements
inferred← citeshttps://doi.org/10.1002/ps.8963openalex-snapshot
Growth inhibition of arable weeds by cerato‐platanin, a plant immune defense activator of fungal origin
inferred← citeshttps://doi.org/10.1002/slct.202503609openalex-snapshot
Biochemical Mechanisms Underlying Resistance to Alternaria alternata f.sp. mali in Apple Genotypes
inferred← citeshttps://doi.org/10.1007/124_2020_45openalex-snapshot
The Haustorium of Phytopathogenic Fungi: A Short Overview of a Specialized Cell of Obligate Biotrophic Plant Parasites
inferred← citeshttps://doi.org/10.1007/978-1-0716-1613-0_16openalex-snapshot
Isolation and Functional Analysis of Effector Proteins of Magnaporthe oryzae
inferred← citeshttps://doi.org/10.1007/978-1-4614-5001-6_16openalex-snapshot
Plant Pathogen Interactions: Crop Improvement Under Adverse Conditions
inferred← citeshttps://doi.org/10.1007/978-1-61779-501-5_38openalex-snapshot
Isolation of Apoplastic Fluid from Leaf Tissue by the Vacuum Infiltration-Centrifugation Technique
inferred← citeshttps://doi.org/10.1007/978-3-030-21270-4_3openalex-snapshot
Overview of Genomic Resources Available for Lupins with a Focus on Narrow-Leafed Lupin (Lupinus angustifolius)
inferred← citeshttps://doi.org/10.1007/978-3-030-27165-7_1openalex-snapshot
Bioactive Molecules from Bacillus spp.: An Effective Tool for Plant Stress Management
inferred← citeshttps://doi.org/10.1007/978-3-030-48733-1_15openalex-snapshot
Protein Phosphatase Mediated Responses in Plant Host-Pathogen Interactions
inferred← citeshttps://doi.org/10.1007/978-3-030-93390-6_8openalex-snapshot
Genomic Advances in Research on Genetic Resistance to White Pine Blister Rust in North American White Pines
inferred← citeshttps://doi.org/10.1007/978-3-031-08072-2_12openalex-snapshot
Genome Editing in Plants for Resistance Against Bacterial Pathogens
inferred← citeshttps://doi.org/10.1007/978-3-031-16503-0_18openalex-snapshot
Magnaporthe oryzae and Its Pathotypes: A Potential Plant Pandemic Threat to Global Food Security
inferred← citeshttps://doi.org/10.1007/978-3-031-24181-9_8openalex-snapshot
Microbial Elicitors for Priming Plant Defense Mechanisms
inferred← citeshttps://doi.org/10.1007/978-3-031-81639-0_1openalex-snapshot
Applications, Challenges, and Future Perspectives of Omics in Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-031-85340-1_17openalex-snapshot
Pattern Recognition Receptors in Plant Immunity
inferred← citeshttps://doi.org/10.1007/978-3-319-08575-3_10openalex-snapshot
Plant Pathogenic Fungi and Oomycetes
inferred← citeshttps://doi.org/10.1007/978-3-319-23371-0_12openalex-snapshot
Infection Process and Fungal Virulence Factors
inferred← citeshttps://doi.org/10.1007/978-3-319-26118-8_2openalex-snapshot
Role of Plant Immune Signals and Signaling Systems in Plant Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-29573-2_12openalex-snapshot
Mycorrhizal Association: A Safeguard for Plant Pathogen
inferred← citeshttps://doi.org/10.1007/978-3-319-42319-7_4openalex-snapshot
Belowground Defence Strategies Against Fusarium oxysporum
inferred← citeshttps://doi.org/10.1007/978-3-319-42319-7_6openalex-snapshot
Belowground Defence Strategies Against Verticillium Pathogens
inferred← citeshttps://doi.org/10.1007/978-3-319-46340-7_2openalex-snapshot
Plant Small Heat Shock Proteins and Its Interactions with Biotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-92528-8_14openalex-snapshot
A Genomic View of Biotic Stress Resistance
inferred← citeshttps://doi.org/10.1007/978-3-642-30141-4_62openalex-snapshot
Virulence Strategies of Plant Pathogenic Bacteria
inferred← citeshttps://doi.org/10.1007/978-3-642-37241-4_13openalex-snapshot
Induction of Plant Defense Response and Its Impact on Productivity
inferred← citeshttps://doi.org/10.1007/978-3-642-41787-0_9openalex-snapshot
Endocytosis: At the Crossroads of Pattern Recognition Immune Receptors and Pathogen Effectors
inferred← citeshttps://doi.org/10.1007/978-3-642-42011-5_11openalex-snapshot
Lipases in Signaling Plant Defense Responses
inferred← citeshttps://doi.org/10.1007/978-3-642-55378-3_3openalex-snapshot
Ecological Genomics of Pseudomonas syringae
inferred← citeshttps://doi.org/10.1007/978-3-662-44056-8_4openalex-snapshot
Verticillium alfalfae and V . dahliae, Agents of Verticillium Wilt Diseases
inferred← citeshttps://doi.org/10.1007/978-94-007-7426-1_2openalex-snapshot
PAMP Signaling in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_2openalex-snapshot
Salicylic Acid Signaling in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_4openalex-snapshot
Ethylene Signaling System in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-981-10-6847-8_2openalex-snapshot
Antimycotic Role of Soil Bacillus sp. Against Rice Pathogens: A Biocontrol Prospective
inferred← citeshttps://doi.org/10.1007/978-981-10-7371-7_15openalex-snapshot
Plant Cell Wall: A Simple Physical Barrier or a Complex Defense Modulator – Exploring Its Dynamic Role at Plant-Fungus Interface
inferred← citeshttps://doi.org/10.1007/978-981-10-7371-7_4openalex-snapshot
Pathogen-Associated Molecular Patterns and Their Perception in Plants
inferred← citeshttps://doi.org/10.1007/978-981-15-1322-0_22openalex-snapshot
Biological Host Response: A Paradigm and Strategy to Overcome Biotic Stress Caused by Powdery Mildew Causal Agents in Plants
inferred← citeshttps://doi.org/10.1007/978-981-15-9154-9_1openalex-snapshot
Microbial Interactions in the Rhizosphere Contributing Crop Resilience to Biotic and Abiotic Stresses
inferred← citeshttps://doi.org/10.1007/978-981-15-9380-2_12openalex-snapshot
Unraveling the Molecular Mechanism of Magnaporthe oryzae Induced Signaling Cascade in Rice
inferred← citeshttps://doi.org/10.1007/978-981-16-0862-9_1openalex-snapshot
Principles of Host Resistance
inferred← citeshttps://doi.org/10.1007/978-981-16-0862-9_5openalex-snapshot
Host Resistance Signaling Network System to Multiple Stresses
inferred← citeshttps://doi.org/10.1007/978-981-16-0862-9_8openalex-snapshot
Genomics of Host Resistance at a Glance
inferred← citeshttps://doi.org/10.1007/978-981-16-1974-8_6openalex-snapshot
Glimpses of Host Resistance Genomics
inferred← citeshttps://doi.org/10.1007/978-981-16-2956-3_6openalex-snapshot
Harnessing Perks of MiRNA Principles for Betterment of Agriculture and Food Security
inferred← citeshttps://doi.org/10.1007/978-981-16-4449-8_14openalex-snapshot
Common Bunt and Smuts in Wheat and Barley Genetics, Breeding, and Management: Current Status and Future Prospects
inferred← citeshttps://doi.org/10.1007/978-981-16-8918-5_4openalex-snapshot
Soil Bacillus as Biocontrol Agent: Prospects and Applications
inferred← citeshttps://doi.org/10.1007/978-981-19-9884-3_11openalex-snapshot
ROS as Signaling Molecule Under Unfavorable Conditions
inferred← citeshttps://doi.org/10.1007/978-981-95-8601-1_6openalex-snapshot
Interaction of Pathogenic Fungi with Host Cells: Molecular and Cellular Mechanisms
inferred← citeshttps://doi.org/10.1007/978-981-95-8601-1_8openalex-snapshot
Molecular Mechanisms of PAMP-Triggered Immunity in Plant-Pathogen Interactions
inferred← citeshttps://doi.org/10.1007/978-981-96-8869-2_9openalex-snapshot
Melatonin Involvement in PAMP-Triggered Immunity (PTI) and Effector-Triggered Immunity (ETI) Against Fungal Diseases
inferred← citeshttps://doi.org/10.1007/978-981-97-0680-8_17openalex-snapshot
Response and Resistance Mechanisms of Tea Plants to Biotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-97-6374-0_15openalex-snapshot
Peps, Pathogens, and Pests: Challenges and Opportunities for Usage of Pep Signaling in Sustainable Farming
inferred← citeshttps://doi.org/10.1007/978-981-99-9482-3_10openalex-snapshot
Plant-Microbe Interaction to Improve Soil Health
inferred← citeshttps://doi.org/10.1007/s00122-015-2500-6openalex-snapshot
The Co-4 locus on chromosome Pv08 contains a unique cluster of 18 COK-4 genes and is regulated by immune response in common bean
inferred← citeshttps://doi.org/10.1007/s00122-017-2876-6openalex-snapshot
Genetic dissection of the maize (Zea mays L.) MAMP response
inferred← citeshttps://doi.org/10.1007/s00122-018-3055-0openalex-snapshot
Mapping resistance to powdery mildew in barley reveals a large-effect nonhost resistance QTL
inferred← citeshttps://doi.org/10.1007/s00122-018-3095-5openalex-snapshot
The gene conferring susceptibility to spot blotch caused by Cochliobolus sativus is located at the Mla locus in barley cultivar Bowman
inferred← citeshttps://doi.org/10.1007/s00122-019-03297-1openalex-snapshot
Contribution of recent technological advances to future resistance breeding
inferred← citeshttps://doi.org/10.1007/s00122-025-04999-5openalex-snapshot
Integrated transcriptome and BSA-seq analysis identifies a novel QTL for Meloidogyne graminicola resistance in rice HuaHang31
inferred← citeshttps://doi.org/10.1007/s00253-018-9009-2openalex-snapshot
CfPDIP1, a novel secreted protein of Colletotrichum falcatum, elicits defense responses in sugarcane and triggers hypersensitive response in tobacco
inferred← citeshttps://doi.org/10.1007/s00253-019-09937-2openalex-snapshot
Secreted protein MoHrip2 is required for full virulence of Magnaporthe oryzae and modulation of rice immunity
inferred← citeshttps://doi.org/10.1007/s00299-013-1546-7openalex-snapshot
A fungal protein elicitor PevD1 induces Verticillium wilt resistance in cotton
inferred← citeshttps://doi.org/10.1007/s00299-014-1633-4openalex-snapshot
Comprehensive analysis of VQ motif-containing gene expression in rice defense responses to three pathogens
inferred← citeshttps://doi.org/10.1007/s00299-014-1667-7openalex-snapshot
RNAseq analysis of cassava reveals similar plant responses upon infection with pathogenic and non-pathogenic strains of Xanthomonas axonopodis pv. manihotis
inferred← citeshttps://doi.org/10.1007/s00299-020-02655-4openalex-snapshot
Targeted plant improvement through genome editing: from laboratory to field
inferred← citeshttps://doi.org/10.1007/s00299-021-02718-0openalex-snapshot
Influence of virus–host interactions on plant response to abiotic stress
inferred← citeshttps://doi.org/10.1007/s00299-021-02812-3openalex-snapshot
Arabidopsis inositol polyphosphate kinases IPK1 and ITPK1 modulate crosstalk between SA-dependent immunity and phosphate-starvation responses
inferred← citeshttps://doi.org/10.1007/s00299-025-03614-7openalex-snapshot
The negative regulated immune mechanism of Skp1-Cullin1-F-box (SCF) E3 ubiquitin ligase-mediated HOS15-dependent responses in banana
inferred← citeshttps://doi.org/10.1007/s00299-025-03667-8openalex-snapshot
Overexpression of a novel CC-NBS-LRR gene NtRPP13 confers enhanced resistance to Ralstonia solanacearum in tobacco
inferred← citeshttps://doi.org/10.1007/s00344-021-10392-5openalex-snapshot
Arbuscular Mycorrhizal Fungi in Conferring Tolerance to Biotic Stresses in Plants
inferred← citeshttps://doi.org/10.1007/s00425-012-1637-7openalex-snapshot
Arsenal of elevated defense proteins fails to protect tomato against Verticillium dahliae
inferred← citeshttps://doi.org/10.1007/s00425-017-2751-3openalex-snapshot
The accumulation of β-aminobutyric acid is controlled by the plant’s immune system
inferred← citeshttps://doi.org/10.1007/s00425-018-2843-8openalex-snapshot
The sesquiterpene botrydial from Botrytis cinerea induces phosphatidic acid production in tomato cell suspensions
inferred← citeshttps://doi.org/10.1007/s00425-018-2869-yopenalex-snapshot
Tomato Ve resistance locus; defense or growth
inferred← citeshttps://doi.org/10.1007/s00425-019-03130-5openalex-snapshot
The transcription factor MYB15 is essential for basal immunity (PTI) in Chinese wild grape
inferred← citeshttps://doi.org/10.1007/s00425-021-03783-1openalex-snapshot
Tomato Ve-resistance locus: resilience in the face of adversity?
inferred← citeshttps://doi.org/10.1007/s00438-019-01573-9openalex-snapshot
A LysM effector protein from the basidiomycete Rhizoctonia solani contributes to virulence through suppression of chitin-triggered immunity
inferred← citeshttps://doi.org/10.1007/s00438-019-01583-7openalex-snapshot
Knockdown of the chitin-binding protein family gene CaChiIV1 increased sensitivity to Phytophthora capsici and drought stress in pepper plants
inferred← citeshttps://doi.org/10.1007/s00709-016-0941-7openalex-snapshot
Jasmonates are induced by the PAMP flg22 but not the cell death-inducing elicitor Harpin in Vitis rupestris
inferred← citeshttps://doi.org/10.1007/s00709-019-01353-7openalex-snapshot
Two grapevine metacaspase genes mediate ETI-like cell death in grapevine defence against infection of Plasmopara viticola
inferred← citeshttps://doi.org/10.1007/s10059-013-2317-6openalex-snapshot
Differential Requirement of Oryza sativa RAR1 in Immune Receptor-Mediated Resistance of Rice to Magnaporthe oryzae
inferred← citeshttps://doi.org/10.1007/s10265-018-1038-5openalex-snapshot
A DREPP protein interacted with PeaT1 from Alternaria tenuissima and is involved in elicitor-induced disease resistance in Nicotiana plants
inferred← citeshttps://doi.org/10.1007/s10327-018-0828-xopenalex-snapshot
MAMP-triggered plant immunity mediated by the LysM-receptor kinase CERK1
inferred← citeshttps://doi.org/10.1007/s10658-013-0314-4openalex-snapshot
Genetics and molecular mechanisms of resistance to powdery mildews in tomato (Solanum lycopersicum) and its wild relatives
inferred← citeshttps://doi.org/10.1007/s10658-016-1109-1openalex-snapshot
Differential expressions of photosynthetic genes provide clues to the resistance mechanism during Fusarium oxysporum f.sp. ciceri race 1 (Foc1) infection in chickpea (Cicer arietinum L.)
inferred← citeshttps://doi.org/10.1007/s10658-019-01788-xopenalex-snapshot
Early transcriptional response of seedling roots to Ralstonia solanacearum in tobacco (Nicotiana tabacum L.)
inferred← citeshttps://doi.org/10.1007/s10658-020-02181-9openalex-snapshot
Fulvia fulva [syn. Cladosporium fulvum, Passalora fulva] races in Argentina are evolving through genetic changes and carry polymorphic avr and ecp gene sequences
inferred← citeshttps://doi.org/10.1007/s10681-017-1900-xopenalex-snapshot
Breeding for mycorrhizal symbiosis: focus on disease resistance
inferred← citeshttps://doi.org/10.1007/s10681-023-03215-zopenalex-snapshot
Mapping of genomic regions linked to stemphylium blight (Stemphylium botryosum Wallr.) resistance in lentil using linkage mapping and marker-trait association analysis
inferred← citeshttps://doi.org/10.1007/s10709-018-0044-9openalex-snapshot
Genetic signatures of plant resistance genes with known function within and between species
inferred← citeshttps://doi.org/10.1007/s10886-012-0134-6openalex-snapshot
Mycorrhiza-Induced Resistance and Priming of Plant Defenses
inferred← citeshttps://doi.org/10.1007/s11032-018-0778-1openalex-snapshot
Exploring the mechanism and efficient use of a durable gene-mediated resistance to bacterial blight disease in rice
inferred← citeshttps://doi.org/10.1007/s11033-021-06344-7openalex-snapshot
Signals in systemic acquired resistance of plants against microbial pathogens
inferred← citeshttps://doi.org/10.1007/s11033-023-08345-0openalex-snapshot
Interactomics in plant defence: progress and opportunities
inferred← citeshttps://doi.org/10.1007/s11101-025-10091-zopenalex-snapshot
Plant–pathogen interaction: chemical mediation in plant signalling and defence
inferred← citeshttps://doi.org/10.1007/s11103-014-0198-5openalex-snapshot
Expression of Arabidopsis sugar transport protein STP13 differentially affects glucose transport activity and basal resistance to Botrytis cinerea
inferred← citeshttps://doi.org/10.1007/s11103-014-0244-3openalex-snapshot
A novel protein elicitor (SsCut) from Sclerotinia sclerotiorum induces multiple defense responses in plants
inferred← citeshttps://doi.org/10.1007/s11103-017-0633-5openalex-snapshot
UBIQUITIN-SPECIFIC PROTEASES function in plant development and stress responses
inferred← citeshttps://doi.org/10.1007/s11103-019-00824-yopenalex-snapshot
GhCyP3 improves the resistance of cotton to Verticillium dahliae by inhibiting the E3 ubiquitin ligase activity of GhPUB17
inferred← citeshttps://doi.org/10.1007/s11104-021-05047-zopenalex-snapshot
Soil and plant health in relation to dynamic sustainment of Eh and pH homeostasis: A review
inferred← citeshttps://doi.org/10.1007/s11240-016-0997-2openalex-snapshot
An efficient transient mesophyll protoplast system for investigation of the innate immunity responses in the rubber tree (Hevea brasiliensis)
inferred← citeshttps://doi.org/10.1007/s11295-016-0987-xopenalex-snapshot
Evidence for different QTL underlying the immune and hypersensitive responses of Eucalyptus globulus to the rust pathogen Puccinia psidii
inferred← citeshttps://doi.org/10.1007/s11295-020-01481-9openalex-snapshot
Functional analysis of rubber tree receptor-like cytoplasmic kinase HbBIK1 in plant root development and immune response
inferred← citeshttps://doi.org/10.1007/s11427-025-3110-3openalex-snapshot
Unraveling plant immunity: from pathogen perception to resistance engineering
inferred← citeshttps://doi.org/10.1007/s11738-018-2672-1openalex-snapshot
Identification of Rehmannia glutinosa L. NB-ARC family proteins and their typical changes under consecutive monoculture stress
inferred← citeshttps://doi.org/10.1007/s11816-026-01058-3openalex-snapshot
Molecular insights into oomycete effectors and plant counter-defenses
inferred← citeshttps://doi.org/10.1007/s12192-013-0445-8openalex-snapshot
Heat shock, with recovery, promotes protection of Nicotiana tabacum during subsequent exposure to Ralstonia solanacearum
inferred← citeshttps://doi.org/10.1007/s12298-016-0378-7openalex-snapshot
Interplay of genes in plant–pathogen interactions: In planta expression and docking studies of a beta 1,3 glucanase gene from Piper colubrinum and a glucanase inhibitor gene from Phytophthora capsici
inferred← citeshttps://doi.org/10.1007/s12374-017-0209-6openalex-snapshot
Comparative Transcriptome Analysis of Rhizoctonia solani-resistant and -Susceptible Rice Cultivars Reveals the Importance of Pathogen Recognition and Active Immune Responses in Host Resistance
inferred← citeshttps://doi.org/10.1007/s13580-022-00509-4openalex-snapshot
Induction of defense responses related to scavenging reactive oxygen species in Ampelopsis species inoculated with Rhizobium vitis
inferred← citeshttps://doi.org/10.1007/s40362-014-0025-zopenalex-snapshot
The Role of Calmodulin and Related Proteins in Plant Cell Function: An Ever-Thickening Plot
inferred← citeshttps://doi.org/10.1007/s42161-022-01061-xopenalex-snapshot
Comparative transcriptomics and multiple phytohormone profiling reveals the molecular immune response of Arabidopsis thaliana to the pathogen Ralstonia solanacearum type III effector RipN
inferred← citeshttps://doi.org/10.1007/s44154-026-00336-yopenalex-snapshot
Molecular and transcriptional regulation of plant defense responses to aphid infestation
inferred← citeshttps://doi.org/10.1016/b978-0-08-100596-5.00240-7openalex-snapshot
Necrotrophic Pathogens of Wheat
inferred← citeshttps://doi.org/10.1016/b978-0-12-385851-1.00002-0openalex-snapshot
The Molecular Mechanisms of Rice Resistance to the Bacterial Blight Pathogen, Xanthomonas oryzae pathovar oryzae
inferred← citeshttps://doi.org/10.1016/b978-0-12-394437-5.00240-0openalex-snapshot
Necrotrophic Pathogens of Wheat
inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00010-8openalex-snapshot
Metabolic Responses of Plants Upon Different Plant–Pathogen Interactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-816030-5.00001-xopenalex-snapshot
Engineering plant leucine rich repeat-receptors for enhanced pattern-triggered immunity (PTI) and effector-triggered immunity (ETI)
inferred← citeshttps://doi.org/10.1016/b978-0-12-819453-9.00005-2openalex-snapshot
Chemical communication between Trichoderma and plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90594-7.00010-7openalex-snapshot
Evolutionary history of plant receptor-like kinases
inferred← citeshttps://doi.org/10.1016/b978-0-323-91734-6.00010-7openalex-snapshot
The role of Trichoderma fungi in inducing defense mechanisms in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00013-6openalex-snapshot
Volatile compounds–mediated hormonal signaling and crosstalk with plant growth–promoting microbes
inferred← citeshttps://doi.org/10.1016/b978-0-323-95502-7.00104-4openalex-snapshot
Metaproteomics – A Concise Two Decade Journey
inferred← citeshttps://doi.org/10.1016/b978-0-443-13236-0.00002-6openalex-snapshot
Origin and evolutionary history of defense-related proteins in plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-15278-8.00003-6openalex-snapshot
Resistance: the genotype
inferred← citeshttps://doi.org/10.1016/b978-0-443-40316-3.00003-5openalex-snapshot
Comparative genomics: insights into enhancing disease resistance in crops
inferred← citeshttps://doi.org/10.1016/b978-0-444-52512-3.00165-0openalex-snapshot
Plant Disease and Resistance
inferred← citeshttps://doi.org/10.1016/b978-0-444-63987-5.00006-2openalex-snapshot
Innate Immunity Engaged or Disengaged in Plant-Microbe Interactions ☆
inferred← citeshttps://doi.org/10.1016/bs.abr.2015.07.002openalex-snapshot
Molecular Patterns of Rhizobacteria Involved in Plant Immunity Elicitation
inferred← citeshttps://doi.org/10.1016/bs.enz.2016.09.003openalex-snapshot
Receptor-Like Kinases and Regulation of Plant Innate Immunity
inferred← citeshttps://doi.org/10.1016/j.abiote.2026.100042openalex-snapshot
Coordination of PTI and ETI in legume–rhizobium mutualism
inferred← citeshttps://doi.org/10.1016/j.algal.2025.104093openalex-snapshot
Marine algae oligosaccharides: Eco-friendly elicitors for sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.01.017openalex-snapshot
Biochemical characterization of the tomato phosphatidylinositol-specific phospholipase C (PI-PLC) family and its role in plant immunity
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.01.038openalex-snapshot
BcGs1, a glycoprotein from Botrytis cinerea , elicits defence response and improves disease resistance in host plants
inferred← citeshttps://doi.org/10.1016/j.biori.2020.01.002openalex-snapshot
Plant NLR receptor proteins and their potential in the development of durable genetic resistance to biotic stresses
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2015.01.004openalex-snapshot
Bio-based resistance inducers for sustainable plant protection against pathogens
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2023.108296openalex-snapshot
Recombinant production of antimicrobial peptides in plants
inferred← citeshttps://doi.org/10.1016/j.cell.2023.12.030openalex-snapshot
Dual phosphorylation of DGK5-mediated PA burst regulates ROS in plant immunity
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117030openalex-snapshot
Decoding Arabidopsis growth-defense trade-offs through ADR1-associated transcriptional networks
inferred← citeshttps://doi.org/10.1016/j.chom.2018.08.007openalex-snapshot
The MAP4 Kinase SIK1 Ensures Robust Extracellular ROS Burst and Antibacterial Immunity in Plants
inferred← citeshttps://doi.org/10.1016/j.coi.2024.102457openalex-snapshot
Friendly fire: recognition of self by the innate immune system
inferred← citeshttps://doi.org/10.1016/j.cois.2015.04.002openalex-snapshot
Impacts of insect oral secretions on defoliation-induced plant defense
inferred← citeshttps://doi.org/10.1016/j.cpb.2026.100597openalex-snapshot
S genes for disease resistance in wheat using Arabidopsis as a model
inferred← citeshttps://doi.org/10.1016/j.cub.2021.04.080openalex-snapshot
Plant immunity: Crosstalk between plant immune receptors
inferred← citeshttps://doi.org/10.1016/j.cub.2026.08.066openalex-snapshot
A bacterial effector triggers dual-layer plant immunity through interaction with cell-surface and intracellular proteins
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2013.11.014openalex-snapshot
Can adaptation to metalliferous environments affect plant response to biotic stress? Insight from Silene paradoxa L. and phytoalexins
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.06.001openalex-snapshot
Lipid profiling of barley root in interaction with Fusarium macroconidia
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105737openalex-snapshot
Insights into the effects of elevated atmospheric carbon dioxide on plant-virus interactions: A literature review
inferred← citeshttps://doi.org/10.1016/j.fbr.2016.04.001openalex-snapshot
Form and function of fungal and oomycete effectors
inferred← citeshttps://doi.org/10.1016/j.fbr.2019.10.001openalex-snapshot
Twenty years of research on cerato-platanin family proteins: clues, conclusions, and unsolved issues
inferred← citeshttps://doi.org/10.1016/j.fgb.2015.03.015openalex-snapshot
FPLC and liquid-chromatography mass spectrometry identify candidate necrosis-inducing proteins from culture filtrates of the fungal wheat pathogen Zymoseptoria tritici
inferred← citeshttps://doi.org/10.1016/j.fgb.2015.08.010openalex-snapshot
Mind the gap; seven reasons to close fragmented genome assemblies
inferred← citeshttps://doi.org/10.1016/j.gene.2017.04.051openalex-snapshot
LTR-retrotransposons in plants: Engines of evolution
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146983openalex-snapshot
Cotton Mi-1.2-like Gene: A potential source of whitefly resistance
inferred← citeshttps://doi.org/10.1016/j.heliyon.2025.e41769openalex-snapshot
Biological control of bacterial leaf blight (BLB) in rice–A sustainable approach
inferred← citeshttps://doi.org/10.1016/j.hpj.2022.04.008openalex-snapshot
Understanding the mechanisms of resistance to tomato leaf mold: A review
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.09.085openalex-snapshot
Structure-function analysis reveals Trichoderma virens Tsp1 to be a novel fungal effector protein modulating plant defence
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.126891openalex-snapshot
Integrative transcriptomic analysis unveils lncRNA-miRNA-mRNA interplay in tomato plants responding to Ralstonia solanacearum
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.134918openalex-snapshot
Alternaria solani core effector Aex59 is a new member of the Alt a 1 protein family and is recognized as a PAMP
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.136947openalex-snapshot
A conserved extracellular effector protein Ssh1296 from Scleromitrula shiraiana triggers cell death and regulates plant immunity
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.138189openalex-snapshot
A novel type III effector RipBU from Ralstonia solanacearum suppresses plant immunity and promotes peanut susceptibility
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144066openalex-snapshot
Genome-wide identification and characterization of pathogenesis related protein 1 gene family in Brassica juncea
inferred← citeshttps://doi.org/10.1016/j.immuni.2024.03.007openalex-snapshot
The conceptual foundations of innate immunity: Taking stock 30 years later
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.02.005openalex-snapshot
From molecule to cell: the expanding frontiers of plant immunity
inferred← citeshttps://doi.org/10.1016/j.jia.2023.06.014openalex-snapshot
Basal defense is enhanced in a wheat cultivar resistant to Fusarium head blight
inferred← citeshttps://doi.org/10.1016/j.jia.2024.03.002openalex-snapshot
The glycoside hydrolase 7 member VdGH7a regulates Verticillium dahliae pathogenicity and induces host defenses by interacting with GhOLP1
inferred← citeshttps://doi.org/10.1016/j.jia.2024.09.033openalex-snapshot
Glycosylphosphatidylinositol (GPI) anchoring controls cell wall integrity, immune evasion and surface localization of ChFEM1 for infection of Cochlibolus heterostrophus
inferred← citeshttps://doi.org/10.1016/j.jksus.2021.101652openalex-snapshot
Effect of two protein elicitors extracted from Alternaria tenuissima and Beauveria bassiana against rice leaf folder (Marasmia exigua)
inferred← citeshttps://doi.org/10.1016/j.jplph.2011.09.005openalex-snapshot
Warriors at the gate that never sleep: Non-host resistance in plants
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153738openalex-snapshot
Bacterial cyclodipeptides elicit Arabidopsis thaliana immune responses reducing the pathogenic effects of Pseudomonas aeruginosa PAO1 strains on plant development
inferred← citeshttps://doi.org/10.1016/j.jprot.2017.05.020openalex-snapshot
Comparative secretome analysis of Colletotrichum falcatum identifies a cerato-platanin protein (EPL1) as a potential pathogen-associated molecular pattern (PAMP) inducing systemic resistance in sugarcane
inferred← citeshttps://doi.org/10.1016/j.jprot.2018.04.015openalex-snapshot
A proteomic insight into the MSP1 and flg22 induced signaling in Oryza sativa leaves
inferred← citeshttps://doi.org/10.1016/j.mib.2019.08.003openalex-snapshot
Beyond pathogens: microbiota interactions with the plant immune system
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