| P50 | author | Axel Mithöfer | Q40741990 |
| | Massimo Maffei | Q42716491 |
| P2093 | author name string | Gen-Ichiro Arimura | |
| P2860 | cites work | The relative importance of allelopathy in interference: the effects of an invasive weed on a native bunchgrass | Q88159574 |
| | Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves | Q24556763 |
| | Systemins: a functionally defined family of peptide signals that regulate defensive genes in Solanaceae species | Q24619394 |
| | Strigolactones: chemical signals for fungal symbionts and parasitic weeds in plant roots | Q24648811 |
| | A plant pathogen virulence factor inhibits the eukaryotic proteasome by a novel mechanism | Q27650301 |
| | The plant immune system | Q28131801 |
| | The tomato brassinosteroid receptor BRI1 increases binding of systemin to tobacco plasma membranes, but is not involved in systemin signaling | Q28243279 |
| | An endogenous peptide signal in Arabidopsis activates components of the innate immune response | Q28247122 |
| | Are innate immune signaling pathways in plants and animals conserved? | Q28273570 |
| | Sorgoleone | Q28279496 |
| | System potentials, a novel electrical long-distance apoplastic signal in plants, induced by wounding | Q28306152 |
| | Biogeographical variation in community response to root allelochemistry: novel weapons and exotic invasion | Q28315677 |
| | Molecular interactions between the specialist herbivore Manduca sexta (Lepidoptera, Sphingidae) and its natural host Nicotiana attenuata. III. Fatty acid-amino acid conjugates in herbivore oral secretions are necessary and sufficient for [...] | Q28346651 |
| | An Elicitor of Plant Volatiles from Beet Armyworm Oral Secretion | Q28575413 |
| | Ginkgo biloba responds to herbivory by activating early signaling and direct defenses | Q28731028 |
| | Structural requirements of strigolactones for hyphal branching in AM fungi | Q28750428 |
| | FLS2 | Q29541156 |
| | Innate immunity: the virtues of a nonclonal system of recognition | Q29614428 |
| | A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors | Q29618149 |
| | Pep-13, a plant defense-inducing pathogen-associated pattern from Phytophthora transglutaminases. | Q30320728 |
| | Innate immunity in plants and animals: emerging parallels between the recognition of general elicitors and pathogen-associated molecular patterns | Q30320786 |
| | Within-plant signaling by volatiles leads to induction and priming of an indirect plant defense in nature | Q30479175 |
| | Allelopathy and exotic plant invasion: from molecules and genes to species interactions | Q33338706 |
| | Allelopathic effects of volatile monoterpenoids produced by Salvia leucophylla: Inhibition of cell proliferation and DNA synthesis in the root apical meristem of Brassica campestris seedlings | Q33341520 |
| | The rules of engagement in the legume-rhizobial symbiosis. | Q33351989 |
| | Purification of novel protein elicitor from Botrytis cinerea that induces disease resistance and drought tolerance in plants | Q33483964 |
| | Acquired immunity to herbivory and allelopathy caused by airborne plant emissions | Q33639259 |
| | Tissue-type specific systemin perception and the elusive systemin receptor | Q33717099 |
| | Bacterial elicitation and evasion of plant innate immunity | Q33742757 |
| | Herbivory-induced volatiles elicit defence genes in lima bean leaves. | Q33914748 |
| | Recent advances in plant early signaling in response to herbivory. | Q33957820 |
| | The phytotoxic lichen metabolite, usnic acid, is a potent inhibitor of plantp-hydroxyphenylpyruvate dioxygenase | Q55112606 |
| | Biogenic volatile organic compounds from an invasive species: impacts on plant–plant interactions | Q56770886 |
| | Chapter 5 Systemic Acquired Resistance | Q57374083 |
| | Elicitins, Proteinaceous Elicitors of Plant Defense, Are a New Class of Sterol Carrier Proteins | Q57643061 |
| | The fungal elicitor cryptogein is a sterol carrier protein | Q57643071 |
| | A Plant miRNA Contributes to Antibacterial Resistance by Repressing Auxin Signaling | Q57748263 |
| | Metabolic priming by a secreted fungal effector | Q59068382 |
| | Chitooligosaccharide sensing and downstream signaling: contrasted outcomes in pathogenic and beneficial plant-microbe interactions. | Q37773167 |
| | Dual action of the active oxygen species during plant stress responses | Q33966702 |
| | GABA in plants: just a metabolite? | Q33976402 |
| | Hydrogen peroxide homeostasis: activation of plant catalase by calcium/calmodulin | Q34021797 |
| | The systemin receptor SR160 from Lycopersicon peruvianum is a member of the LRR receptor kinase family | Q34036206 |
| | The composite effect of transgenic plant volatiles for acquired immunity to herbivory caused by inter-plant communications | Q34055455 |
| | New insights into plant responses to the attack from insect herbivores | Q34127348 |
| | Lipase activity in insect oral secretions mediates defense responses in Arabidopsis | Q34183052 |
| | The Ustilago maydis effector Pep1 suppresses plant immunity by inhibition of host peroxidase activity | Q34270422 |
| | Cytokinin-mediated control of leaf longevity by AHK3 through phosphorylation of ARR2 in Arabidopsis | Q34270732 |
| | Pectins: structure, biosynthesis, and oligogalacturonide-related signaling | Q34291904 |
| | Common and contrasting themes of plant and animal diseases | Q34292177 |
| | Innate immunity in plants and animals: striking similarities and obvious differences. | Q34327266 |
| | A functional genomics approach identifies candidate effectors from the aphid species Myzus persicae (green peach aphid). | Q34331193 |
| | Induction of Bradyrhizobium japonicum common nod genes by isoflavones isolated from Glycine max. | Q34357113 |
| | (Z)-3-Hexenol induces defense genes and downstream metabolites in maize | Q34376554 |
| | Two LysM receptor molecules, CEBiP and OsCERK1, cooperatively regulate chitin elicitor signaling in rice. | Q34378470 |
| | Recruitment of entomopathogenic nematodes by insect-damaged maize roots | Q34409563 |
| | Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. | Q34425053 |
| | Plant microRNA: a small regulatory molecule with big impact | Q34472479 |
| | Perception of the bacterial PAMP EF-Tu by the receptor EFR restricts Agrobacterium-mediated transformation. | Q34528524 |
| | Systemic acquired resistance. | Q34549706 |
| | Herbivore-induced, indirect plant defences | Q34557797 |
| | beta-Glucosidase: an elicitor of herbivore-induced plant odor that attracts host-searching parasitic wasps | Q34562814 |
| | Early herbivore alert: insect eggs induce plant defense | Q34567726 |
| | Characterization of a BAHD acyltransferase responsible for producing the green leaf volatile (Z)-3-hexen-1-yl acetate in Arabidopsis thaliana | Q34590172 |
| | The strigolactone story | Q34622203 |
| | Strigolactones and root infestation by plant-parasitic Striga, Orobanche and Phelipanche spp. | Q34627773 |
| | Regulation of the plant defence response in arbuscular mycorrhizal symbiosis | Q34647033 |
| | Rapid changes in tree leaf chemistry induced by damage: evidence for communication between plants | Q34681042 |
| | Fragments of ATP synthase mediate plant perception of insect attack. | Q34695548 |
| | Chemical and molecular ecology of herbivore-induced plant volatiles: proximate factors and their ultimate functions. | Q34952912 |
| | Grasses and gall midges: plant defense and insect adaptation. | Q35013609 |
| | Plant cells recognize chitin fragments for defense signaling through a plasma membrane receptor | Q35131204 |
| | The role of effectors of biotrophic and hemibiotrophic fungi in infection. | Q35555895 |
| | Phenolics and plant allelopathy. | Q37817686 |
| | Innate immunity effectors and virulence factors in symbiosis. | Q37826862 |
| | Activation of plant pattern-recognition receptors by bacteria. | Q37826863 |
| | The evolution of symbiotic systems | Q37851394 |
| | Roles of arbuscular mycorrhizas in plant nutrition and growth: new paradigms from cellular to ecosystem scales | Q37851490 |
| | Lipo-chitooligosaccharide signaling in endosymbiotic plant-microbe interactions | Q37862243 |
| | Engineering plant resistance by constructing chimeric receptors that recognize damage-associated molecular patterns (DAMPs). | Q37871127 |
| | Antibiotic activities of host defense peptides: more to it than lipid bilayer perturbation. | Q37880638 |
| | Convergent or parallel molecular evolution of momilactone A and B: potent allelochemicals, momilactones have been found only in rice and the moss Hypnum plumaeforme | Q37881105 |
| | Strigolactones are regulators of root development | Q37884530 |
| | Plant volatiles: production, function and pharmacology | Q37889127 |
| | Effector proteins that modulate plant--insect interactions | Q37891447 |
| | Protein kinase signaling networks in plant innate immunity | Q37894375 |
| | New insights in plant immunity signaling activation. | Q37896859 |
| | The role of chitin detection in plant--pathogen interactions | Q37920391 |
| | The ecosystem and evolutionary contexts of allelopathy | Q37932772 |
| | Nuclear dynamics during plant innate immunity | Q37939389 |
| | TAL effectors: customizable proteins for DNA targeting | Q37940951 |
| | Oomycete and fungal effector entry, a microbial Trojan horse | Q37992066 |
| | Effector-mediated suppression of chitin-triggered immunity by magnaporthe oryzae is necessary for rice blast disease | Q38328397 |
| | Damage-induced resistance in sagebrush: volatiles are key to intra- and interplant communication | Q39121094 |
| | Direct ubiquitination of pattern recognition receptor FLS2 attenuates plant innate immunity. | Q39945752 |
| | Alamethicin and related membrane channel forming polypeptides. | Q40134587 |
| | Release and activity of allelochemicals from allelopathic rice seedlings. | Q40511109 |
| | Short signalling distances make plant communication a soliloquy | Q41140744 |
| | Caterpillar- and salivary-specific modification of plant proteins. | Q42019627 |
| | The role of abscisic acid and water stress in root herbivore-induced leaf resistance | Q42019727 |
| | Diet-specific salivary gene expression and glucose oxidase activity in Spodoptera exigua (Lepidoptera: Noctuidae) larvae | Q42020161 |
| | Robotic mechanical wounding (MecWorm) versus herbivore-induced responses: early signaling and volatile emission in Lima bean (Phaseolus lunatus L.). | Q42020680 |
| | Priming defense genes and metabolites in hybrid poplar by the green leaf volatile cis-3-hexenyl acetate. | Q42028191 |
| | Simultaneous feeding by aboveground and belowground herbivores attenuates plant-mediated attraction of their respective natural enemies. | Q42032103 |
| | Fatty acid amides, previously identified in caterpillars, found in the cricket Teleogryllus taiwanemma and fruit fly Drosophila melanogaster larvae | Q42032995 |
| | Within-plant signalling via volatiles overcomes vascular constraints on systemic signalling and primes responses against herbivores | Q42033367 |
| | Cowpea chloroplastic ATP synthase is the source of multiple plant defense elicitors during insect herbivory | Q42034095 |
| | Oral secretions from herbivorous lepidopteran larvae exhibit ion channel-forming activities | Q42034446 |
| | Priming of plant defense responses in nature by airborne signaling between Artemisia tridentata and Nicotiana attenuata | Q42038458 |
| | Effects of feeding Spodoptera littoralis on lima bean leaves. III. Membrane depolarization and involvement of hydrogen peroxide. | Q42038524 |
| | Effects of feeding Spodoptera littoralis on lima bean leaves. I. Membrane potentials, intracellular calcium variations, oral secretions, and regurgitate components. | Q42045154 |
| | N-(17-Phosphonooxylinolenoyl)glutamine and N-(17-phosphonooxylinoleoyl)glutamine from insect gut: the first backbone-phosphorylated fatty acid derivatives in nature. | Q42045561 |
| | A plasma membrane protein from Zea mays binds with the herbivore elicitor volicitin | Q42045676 |
| | N-(17-Acyloxy-acyl)-glutamines: Novel Surfactants from Oral Secretions of Lepidopteran Larvae† | Q42046186 |
| | Gut bacteria may be involved in interactions between plants, herbivores and their predators: microbial biosynthesis of N-acylglutamine surfactants as elicitors of plant volatiles | Q42055573 |
| | Induction as well as suppression: How aphid saliva may exert opposite effects on plant defense | Q42146810 |
| | 11C-imaging: methyl jasmonate moves in both phloem and xylem, promotes transport of jasmonate, and of photoassimilate even after proton transport is decoupled | Q42172036 |
| | The lysin motif receptor-like kinase (LysM-RLK) CERK1 is a major chitin-binding protein in Arabidopsis thaliana and subject to chitin-induced phosphorylation | Q42428016 |
| | The transcriptome of cis-jasmone-induced resistance in Arabidopsis thaliana and its role in indirect defence | Q42936811 |
| | The Pseudomonas syringae phytotoxin coronatine promotes virulence by overcoming salicylic acid-dependent defences in Arabidopsis thaliana | Q43010978 |
| | Innate immunity in plants: an arms race between pattern recognition receptors in plants and effectors in microbial pathogens | Q43066417 |
| | PEPR2 is a second receptor for the Pep1 and Pep2 peptides and contributes to defense responses in Arabidopsis. | Q43152590 |
| | Salicylic acid is a modulator of catalase isozymes in chickpea plants infected with Fusarium oxysporum f. sp. ciceri | Q43452997 |
| | Effect of (+)-pulegone and other oil components of Mentha x Piperita on cucumber respiration. | Q43597006 |
| | Analysis of two in planta expressed LysM effector homologs from the fungus Mycosphaerella graminicola reveals novel functional properties and varying contributions to virulence on wheat. | Q43617007 |
| | Effect of Mentha x piperita essential oil and monoterpenes on cucumber root membrane potential | Q43774433 |
| | THE OXIDATIVE BURST IN PLANT DISEASE RESISTANCE. | Q44073104 |
| | A putative lipid transfer protein involved in systemic resistance signalling in Arabidopsis | Q44157351 |
| | A highly conserved effector in Fusarium oxysporum is required for full virulence on Arabidopsis | Q44187058 |
| | Cloning the tomato curl3 gene highlights the putative dual role of the leucine-rich repeat receptor kinase tBRI1/SR160 in plant steroid hormone and peptide hormone signaling. | Q44240482 |
| | Structural determination of the lipo-chitin oligosaccharide nodulation signals produced by Rhizobium giardinii bv. giardinii H152. | Q44288546 |
| | The tomato mutant spr1 is defective in systemin perception and the production of a systemic wound signal for defense gene expression | Q44311772 |
| | Brassinosteroid and systemin: two hormones perceived by the same receptor | Q44381018 |
| | Reactive electrophile species activate defense gene expression in Arabidopsis | Q44402991 |
| | Role of the plasma membrane H+-ATPase in auxin-induced elongation growth: historical and new aspects | Q44561210 |
| | Channel properties of template assembled alamethicin tetramers | Q44682067 |
| | ZmPep1, an ortholog of Arabidopsis elicitor peptide 1, regulates maize innate immunity and enhances disease resistance | Q44698306 |
| | Juglone disrupts root plasma membrane H+-ATPase activity and impairs water uptake, root respiration, and growth in soybean (Glycine max) and corn (Zea mays). | Q44867245 |
| | The receptor for the fungal elicitor ethylene-inducing xylanase is a member of a resistance-like gene family in tomato | Q44904965 |
| | Separable fragments and membrane tethering of Arabidopsis RIN4 regulate its suppression of PAMP-triggered immunity | Q45093683 |
| | The N terminus of bacterial elongation factor Tu elicits innate immunity in Arabidopsis plants. | Q45153591 |
| | Glycerol-3-phosphate is a critical mobile inducer of systemic immunity in plants | Q45783109 |
| | Myzus persicae (green peach aphid) salivary components induce defence responses in Arabidopsis thaliana. | Q45950892 |
| | Damaged-self recognition in plant herbivore defence. | Q45961966 |
| | Cloning and characterisation of a maize carotenoid cleavage dioxygenase (ZmCCD1) and its involvement in the biosynthesis of apocarotenoids with various roles in mutualistic and parasitic interactions. | Q46033932 |
| | Role of benzoxazinones in allelopathy by rye (Secale cereale L.). | Q46044966 |
| | Volatile C6-aldehydes and Allo-ocimene activate defense genes and induce resistance against Botrytis cinerea in Arabidopsis thaliana | Q46477722 |
| | Plant-plant signaling: ethylene synergizes volatile emission in Zea mays induced by exposure to (Z)-3-hexen-1-ol. | Q46678212 |
| | Identification of aphid salivary proteins: a proteomic investigation of Myzus persicae | Q46692728 |
| | Plastid omega3-fatty acid desaturase-dependent accumulation of a systemic acquired resistance inducing activity in petiole exudates of Arabidopsis thaliana is independent of jasmonic acid | Q46844367 |
| | The Arabidopsis her1 mutant implicates GABA in E-2-hexenal responsiveness | Q46923406 |
| | Methyl salicylate is a critical mobile signal for plant systemic acquired resistance | Q46966163 |
| | The HrpN effector of Erwinia amylovora, which is involved in type III translocation, contributes directly or indirectly to callose elicitation on apple leaves | Q47792998 |
| | A polypeptide from tomato leaves induces wound-inducible proteinase inhibitor proteins | Q47894014 |
| | Harpin, elicitor of the hypersensitive response produced by the plant pathogen Erwinia amylovora | Q47932082 |
| | Host-Pathogen Interactions: XI. Composition and Structure of Wall-released Elicitor Fractions | Q47941911 |
| | Isolation and identification of alectrol as (+)-orobanchyl acetate, a germination stimulant for root parasitic plants. | Q50678123 |
| | Interplay between calcium signalling and early signalling elements during defence responses to microbe- or damage-associated molecular patterns. | Q51864348 |
| | Gamma-aminobutyrate: defense against invertebrate pests? | Q52572670 |
| | Volatile Semiochemicals Released from Undamaged Cotton Leaves (A Systemic Response of Living Plants to Caterpillar Damage). | Q52599043 |
| | C6-volatiles derived from the lipoxygenase pathway induce a subset of defense-related genes. | Q54104402 |
| | Wound-induced changes in root and shoot jasmonic acid pools correlate with induced nicotine synthesis inNicotiana sylvestris spegazzini and comes. | Q54197675 |
| | The Arabidopsis receptor kinase FLS2 binds flg22 and determines the specificity of flagellin perception. | Q55041494 |
| | Mode of Action, Localization of Production, Chemical Nature, and Activity of Sorgoleone: A Potent PSII Inhibitor in Sorghum spp. Root Exudates1 | Q55112587 |
| | Polygalacturonases, polygalacturonase-inhibiting proteins and pectic oligomers in plant-pathogen interactions. | Q35661276 |
| | Early signaling in actinorhizal symbioses | Q35672028 |
| | Brassinosteroid signal transduction--choices of signals and receptors | Q35753137 |
| | Bruchins: insect-derived plant regulators that stimulate neoplasm formation. | Q35765229 |
| | Biochemical and physiological mechanisms mediated by allelochemicals | Q35825058 |
| | Energization of transport processes in plants. roles of the plasma membrane H+-ATPase. | Q35890917 |
| | Disulfooxy fatty acids from the American bird grasshopper Schistocerca americana, elicitors of plant volatiles. | Q35928885 |
| | Molecular sabotage of plant defense by aphid saliva | Q35973365 |
| | Airborne signals prime plants against insect herbivore attack | Q36162493 |
| | Herbivores, vascular pathways, and systemic induction: facts and artifacts | Q36273018 |
| | CERK1, a LysM receptor kinase, is essential for chitin elicitor signaling in Arabidopsis | Q36288751 |
| | Strigol: biogenesis and physiological activity | Q36398835 |
| | Green leaf volatiles: hydroperoxide lyase pathway of oxylipin metabolism | Q36440682 |
| | The role of root exudates in rhizosphere interactions with plants and other organisms | Q36466505 |
| | RXLR effector reservoir in two Phytophthora species is dominated by a single rapidly evolving superfamily with more than 700 members | Q36534493 |
| | Allelopathy--a natural alternative for weed control | Q36755520 |
| | Rhizosphere communication of plants, parasitic plants and AM fungi | Q36784776 |
| | Male-derived butterfly anti-aphrodisiac mediates induced indirect plant defense. | Q36786790 |
| | Before gene expression: early events in plant-insect interaction | Q36863218 |
| | Groovy times: filamentous pathogen effectors revealed | Q36870373 |
| | Microbe-associated molecular patterns (MAMPs) probe plant immunity | Q36891333 |
| | Insects feeding on plants: rapid signals and responses preceding the induction of phytochemical release | Q36933888 |
| | Evolution and current status of ecological phytochemistry. | Q37006782 |
| | Recognition of herbivory-associated molecular patterns | Q37100629 |
| | Long-distance signalling in plant defence. | Q37166887 |
| | Belowground ABA boosts aboveground production of DIMBOA and primes induction of chlorogenic acid in maize | Q37261523 |
| | Diversity, regulation, and evolution of the gibberellin biosynthetic pathway in fungi compared to plants and bacteria | Q37533370 |
| | Recent advances in PAMP-triggered immunity against bacteria: pattern recognition receptors watch over and raise the alarm | Q37533855 |
| | Benzoxazinoid biosynthesis, a model for evolution of secondary metabolic pathways in plants | Q37541412 |
| | Early molecular events in PAMP-triggered immunity. | Q37553521 |
| | How do plants "notice" attack by herbivorous arthropods? | Q37644533 |
| | Induced systemic resistance and plant responses to fungal biocontrol agents | Q37700634 |
| | Reactive oxygen species during plant-microorganism early interactions. | Q37727369 |
| P433 | issue | 11 | |
| P304 | page(s) | 1288-1303 | |
| P577 | publication date | 2012-11-01 | |
| P1433 | published in | Natural Product Reports | Q2376904 |
| P1476 | title | Natural elicitors, effectors and modulators of plant responses | |
| P478 | volume | 29 | |