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Controlling crop diseases using induced resistance: challenges for the future
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inferredcites →https://doi.org/10.1002/(sici)1096-9063(199708)50:4<275::aid-ps593>3.0.co;2-7openalex-snapshot
The Chemistry of Benzothiadiazole Plant Activators
inferredcites →https://doi.org/10.1002/1526-4998(200011)56:11<989::aid-ps229>3.0.co;2-aopenalex-snapshot
Suppression of grey mould on strawberry fruit with the chemical plant activator acibenzolar
inferredcites →https://doi.org/10.1002/9780470995983.ch1openalex-snapshot
Introduction: Definitions and Some History
inferredcites →https://doi.org/10.1002/9780470995983.ch11openalex-snapshot
Integration of Induced Resistance in Crop Production
inferredcites →https://doi.org/10.1002/9780470995983.ch2openalex-snapshot
Agents That Can Elicit Induced Resistance
inferredcites →https://doi.org/10.1002/9781118371848.ch1openalex-snapshot
Introduction: Definitions and Some History
inferredcites →https://doi.org/10.1002/9781118371848.ch2openalex-snapshot
Agents That Can Elicit Induced Resistance
inferredcites →https://doi.org/10.1002/pmic.200700173openalex-snapshot
Proteome, salicylic acid, and jasmonic acid changes in cucumber plants inoculated with Trichoderma asperellum strain T34
inferredcites →https://doi.org/10.1002/ps.2220openalex-snapshot
Systemic resistance induced in Arabidopsis thaliana by Trichoderma asperellum SKT‐1, a microbial pesticide of seedborne diseases of rice
inferredcites →https://doi.org/10.1002/ps.2277openalex-snapshot
Evaluation of plant‐growth‐promoting rhizobacteria, acibenzolar‐ S ‐methyl and hymexazol for integrated control of Fusarium crown and root rot on tomato
inferredcites →https://doi.org/10.1006/pmpp.1998.0193openalex-snapshot
Signal interactions in pathogen and insect attack: systemic plant-mediated interactions between pathogens and herbivores of the tomato,Lycopersicon esculentum
inferredcites →https://doi.org/10.1006/pmpp.2001.0327openalex-snapshot
The plant defence activator acibenzolar-S-methyl primes cowpea [ Vigna unguiculata(L.) Walp.] seedlings for rapid induction of resistance
inferredcites →https://doi.org/10.1006/pmpp.2002.0385openalex-snapshot
Acibenzolar- S -methyl-induced resistance to sunflower rust (Puccinia helianthi) is associated with an enhancement of coumarins on foliar surface
inferredcites →https://doi.org/10.1007/978-1-4020-8780-6_3openalex-snapshot
Priming: it’s all the world to induced disease resistance
inferredcites →https://doi.org/10.1007/bf02980855openalex-snapshot
Crenate broomrape control in pea by foliar application of benzothiadiazole (BTH)
inferredcites →https://doi.org/10.1007/bf03356321openalex-snapshot
Effects of sulfated polysaccharide and alcoholic extracts from green seaweed Ulva fasciata on anthracnose severity and growth of common bean (Phaseolus vulgaris L.)
inferredcites →https://doi.org/10.1007/s00114-006-0129-7openalex-snapshot
Induced resistance enzymes in wild plants–do ‘early birds’ escape from pathogen attack?
inferredcites →https://doi.org/10.1007/s00217-012-1715-xopenalex-snapshot
Postharvest BTH treatment induced disease resistance and enhanced reactive oxygen species metabolism in muskmelon (Cucumis melo L.) fruit
inferredcites →https://doi.org/10.1007/s00572-006-0051-zopenalex-snapshot
Arbuscular mycorrhiza reduces susceptibility of tomato to Alternaria solani
inferredcites →https://doi.org/10.1007/s00572-007-0122-9openalex-snapshot
Exogenous systemin has a contrasting effect on disease resistance in mycorrhizal tomato (Solanum lycopersicum) plants infected with necrotrophic or hemibiotrophic pathogens
inferredcites →https://doi.org/10.1007/s00572-011-0380-4openalex-snapshot
Induction of DIMBOA accumulation and systemic defense responses as a mechanism of enhanced resistance of mycorrhizal corn (Zea mays L.) to sheath blight
inferredcites →https://doi.org/10.1007/s10535-011-0118-3openalex-snapshot
Thiamine seed treatment enhances LOX expression, promotes growth and induces downy mildew disease resistance in pearl millet
inferredcites →https://doi.org/10.1007/s10658-007-9251-4openalex-snapshot
Priming: it’s all the world to induced disease resistance
inferredcites →https://doi.org/10.1007/s10658-009-9564-6openalex-snapshot
Mechanisms of induced resistance in lettuce against Bremia lactucae by DL-β-amino-butyric acid (BABA)
inferredcites →https://doi.org/10.1007/s10658-010-9582-4openalex-snapshot
Induced resistance in potato to Phytphthora infestans—effects of BABA in greenhouse and field tests with different potato varieties
inferredcites →https://doi.org/10.1007/s10658-010-9599-8openalex-snapshot
Erratum to: Induced resistance in potato to Phytophthora infestans—effects of BABA in greenhouse and field tests with different potato varieties
inferredcites →https://doi.org/10.1007/s10658-010-9678-xopenalex-snapshot
Benzothiadiazole and BABA improve resistance to Uromyces pisi (Pers.) Wint. in Pisum sativum L. with an enhancement of enzymatic activities and total phenolic content
inferredcites →https://doi.org/10.1007/s10658-010-9724-8openalex-snapshot
Post infection application of DL-3-amino-butyric acid (BABA) induces multiple forms of resistance against Bremia lactucae in lettuce
inferredcites →https://doi.org/10.1007/s10658-010-9733-7openalex-snapshot
Existing infection with Rhynchosporium secalis compromises the ability of barley to express induced resistance
inferredcites →https://doi.org/10.1007/s10658-011-9816-0openalex-snapshot
An Ulva armoricana extract protects plants against three powdery mildew pathogens
inferredcites →https://doi.org/10.1007/s10658-011-9897-9openalex-snapshot
β-aminobutyric acid protects Brassica napus plants from infection by Leptosphaeria maculans. Resistance induction or a direct antifungal effect?
inferredcites →https://doi.org/10.1007/s10658-012-0050-1openalex-snapshot
Efficiency of resistance elicitors in the management of grapevine downy mildew Plasmopara viticola: epidemiological, biochemical and economic aspects
inferredcites →https://doi.org/10.1007/s10658-012-9948-xopenalex-snapshot
Control of foliar diseases in barley: towards an integrated approach
inferredcites →https://doi.org/10.1007/s10658-012-9954-zopenalex-snapshot
Effects of fertilizers and plant strengtheners on the susceptibility of tomatoes to single and mixed isolates of Phytophthora infestans
inferredcites →https://doi.org/10.1007/s10658-012-9995-3openalex-snapshot
Domestication affected the basal and induced disease resistance in common bean (Phaseolus vulgaris)
inferredcites →https://doi.org/10.1007/s11103-005-1728-yopenalex-snapshot
Specific patterns of changes in wheat gene expression after treatment with three antifungal compounds
inferredcites →https://doi.org/10.1007/s11104-007-9391-5openalex-snapshot
Mycorrhizal responses to biochar in soil – concepts and mechanisms
inferredcites →https://doi.org/10.1007/s11104-009-0150-7openalex-snapshot
Chemically-induced resistance on soybean inhibits nodulation and mycorrhization
inferredcites →https://doi.org/10.1007/s11104-011-0916-6openalex-snapshot
Protection of strawberry plants (Fragaria ananassa Duch.) against anthracnose disease induced by Azospirillum brasilense
inferredcites →https://doi.org/10.1007/s11104-011-1070-xopenalex-snapshot
Arbuscular mycorrhizal fungi reduce root-knot nematode penetration through altered root exudation of their host
inferredcites →https://doi.org/10.1007/s11104-012-1129-3openalex-snapshot
Biochar mediates systemic response of strawberry to foliar fungal pathogens
inferredcites →https://doi.org/10.1007/s12275-012-1477-yopenalex-snapshot
Biological control and plant growth promoting capacity of rhizobacteria on pepper under greenhouse and field conditions
inferredcites →https://doi.org/10.1016/j.biocontrol.2006.04.014openalex-snapshot
Improvement of biological control capacity of Paenibacillus polymyxa E681 by seed pelleting on sesame
inferredcites →https://doi.org/10.1016/j.biocontrol.2011.04.006openalex-snapshot
Trichoderma harzianum T39 induces resistance against downy mildew by priming for defense without costs for grapevine
inferredcites →https://doi.org/10.1016/j.cropro.2010.08.020openalex-snapshot
Effect of Acibenzolar-S-methyl (ASM) pre-treatment in inducing resistance against Pythium aphanidermatum infection in Curcuma longa
inferredcites →https://doi.org/10.1016/j.cropro.2011.02.023openalex-snapshot
Saccharin-induced systemic acquired resistance against rust (Phakopsora pachyrhizi) infection in soybean: Effects on growth and development
inferredcites →https://doi.org/10.1016/j.cropro.2011.05.019openalex-snapshot
Management of bacterial wilt in tomatoes with thymol and acibenzolar-S-methyl
inferredcites →https://doi.org/10.1016/j.cropro.2011.08.008openalex-snapshot
Farming with fewer pesticides: EU pesticide review and resulting challenges for UK agriculture
inferredcites →https://doi.org/10.1016/j.cropro.2011.08.019openalex-snapshot
Application of acibenzolar-S-methyl and standard fungicides for control of Phytophthora blight on squash
inferredcites →https://doi.org/10.1016/j.cropro.2011.12.001openalex-snapshot
Induction of systemic acquired resistance against rust, ascochyta blight and broomrape in faba bean by exogenous application of salicylic acid and benzothiadiazole
inferredcites →https://doi.org/10.1016/j.cropro.2012.01.008openalex-snapshot
Seed and leaf treatments with natural compounds to induce resistance against Peronospora parasitica in Brassica oleracea
inferredcites →https://doi.org/10.1016/j.cropro.2012.04.028openalex-snapshot
Control of light leaf spot (Pyrenopeziza brassicae) on winter oilseed rape (Brassica napus) with resistance elicitors
inferredcites →https://doi.org/10.1016/j.jplph.2010.08.011openalex-snapshot
Arbuscular mycorrhizal symbiosis decreases strigolactone production in tomato
inferredcites →https://doi.org/10.1016/j.njas.2011.01.001openalex-snapshot
Elicitors and soil management to induce resistance against fungal plant diseases
inferredcites →https://doi.org/10.1016/j.pbi.2007.05.004openalex-snapshot
Unraveling mycorrhiza-induced resistance
inferredcites →https://doi.org/10.1016/j.pedobi.2007.08.002openalex-snapshot
Charcoal and smoke extract stimulate the soil microbial community in a highly weathered xanthic Ferralsol
inferredcites →https://doi.org/10.1016/j.plantsci.2010.07.023openalex-snapshot
Low temperature induced defence gene expression in winter wheat in relation to resistance to snow moulds and other wheat diseases
inferredcites →https://doi.org/10.1016/j.pmpp.2006.01.003openalex-snapshot
Defence responses induced by potassium phosphonate in Phytophthora palmivora-challenged Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.pmpp.2006.11.001openalex-snapshot
Activities of antioxidant enzymes and photosynthetic responses in tomato pre-treated by plant activators and inoculated by Xanthomonas vesicatoria
inferredcites →https://doi.org/10.1016/j.pmpp.2007.09.008openalex-snapshot
Costs and trade-offs associated with induced resistance
inferredcites →https://doi.org/10.1016/j.pmpp.2008.02.002openalex-snapshot
Defense gene expression patterns of three SAR-induced tomato cultivars in the field
inferredcites →https://doi.org/10.1016/j.pmpp.2009.03.002openalex-snapshot
Priming for plant defense in barley provides benefits only under high disease pressure
inferredcites →https://doi.org/10.1016/j.pmpp.2011.02.001openalex-snapshot
Possible trade-off associated with the use of a combination of resistance elicitors
inferredcites →https://doi.org/10.1016/j.postharvbio.2003.09.016openalex-snapshot
Elicitors of induced disease resistance in postharvest horticultural crops: a brief review
inferredcites →https://doi.org/10.1016/j.postharvbio.2010.09.007openalex-snapshot
Biological control agents and chemical inducers of resistance for postharvest control of Penicillium expansum Link. on apple fruit
inferredcites →https://doi.org/10.1016/j.postharvbio.2011.02.008openalex-snapshot
Effects of β-aminobutyric acid on control of postharvest blue mould of apple fruit and its possible mechanisms of action
inferredcites →https://doi.org/10.1016/j.scienta.2011.06.014openalex-snapshot
Expression of PPO and POD genes and contents of polyphenolic compounds in harvested mango fruits in relation to Benzothiadiazole-induced defense against anthracnose
inferredcites →https://doi.org/10.1016/j.scienta.2011.06.024openalex-snapshot
Multiple pre-harvest treatments with acibenzolar-S-methyl reduce latent infection and induce resistance in muskmelon fruit
inferredcites →https://doi.org/10.1016/j.scienta.2012.02.011openalex-snapshot
Induction of natural defence accompanied by salicylic acid-dependant systemic acquired resistance in tomato seedlings in response to bioelicitors isolated from green algae
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.010openalex-snapshot
Evolution of jasmonate and salicylate signal crosstalk
inferredcites →https://doi.org/10.1016/s0885-5765(05)80041-4openalex-snapshot
Systemic translocation of 14C-dl-3-aminobutyric acid in tomato plants in relation to induced resistance against Phytophthora infestans
inferredcites →https://doi.org/10.1016/s0929-1393(02)00037-9openalex-snapshot
Does induced resistance in plants affect the belowground community?
inferredcites →https://doi.org/10.1016/s1049-9644(02)00022-1openalex-snapshot
Mixtures of plant growth-promoting rhizobacteria for induction of systemic resistance against multiple plant diseases
inferredcites →https://doi.org/10.1016/s1360-1385(01)02186-0openalex-snapshot
Fitness costs of induced resistance: emerging experimental support for a slippery concept
inferredcites →https://doi.org/10.1016/s1360-1385(98)01199-6openalex-snapshot
Pathogen defence in plants — a paradigm of biological complexity
inferredcites →https://doi.org/10.1017/s0021859609008806openalex-snapshot
Practical application of induced resistance to plant diseases: an appraisal of effectiveness under field conditions
inferredcites →https://doi.org/10.1021/jf203974popenalex-snapshot
Novel Benzo-1,2,3-thiadiazole-7-carboxylate Derivatives As Plant Activators and the Development of Their Agricultural Applications
inferredcites →https://doi.org/10.1023/a:1001859824008openalex-snapshot
Effect of salicylic acid on nodulation, nitrogenous compounds and related enzymes of Vigna mungo
inferredcites →https://doi.org/10.1023/a:1008683316629openalex-snapshot
Effect of treating soybean with 2,6-dichloroisonicotinic acid (INA) and benzothiadiazole (BTH) on seed yields and the level of disease caused by Sclerotinia sclerotiorum in field and greenhouse studies
inferredcites →https://doi.org/10.1023/a:1008760518772openalex-snapshot
Induced Disease Resistance in Plants by Chemicals
inferredcites →https://doi.org/10.1023/a:1008767719691openalex-snapshot
Foliar Application of Acibenzolar-S-Methyl and Protection of Postharvest Rock Melons and Hami Melons from Disease
inferredcites →https://doi.org/10.1023/a:1011203826805openalex-snapshot
Induction of Systemic Resistance in Cucumber against Several Diseases by Plant Growth-promoting Fungi: lignification and Superoxide Generation
inferredcites →https://doi.org/10.1023/a:1011954828685openalex-snapshot
Pine Wilt Disease Caused by the Pine Wood Nematode: The Induced Resistance of Pine Trees by the Avirulent Isolates of Nematode
inferredcites →https://doi.org/10.1023/a:1016225515936openalex-snapshot
Antagonism Between Jasmonate- and Salicylate-Mediated Induced Plant Resistance: Effects of Concentration and Timing of Elicitation on Defense-Related Proteins, Herbivore, and Pathogen Performance in Tomato
inferredcites →https://doi.org/10.1023/a:1020840900595openalex-snapshot
Trade-Offs in Plant Defense Against Pathogens and Herbivores: A Field Demonstration of Chemical Elicitors of Induced Resistance
inferredcites →https://doi.org/10.1023/a:1022397130895openalex-snapshot
Elicitors of Plant Defensive Systems Reduce Insect Densities and Disease Incidence
inferredcites →https://doi.org/10.1023/a:1026543126341openalex-snapshot
Interactions between Plasmopara helianthi, Glomus mosseae and Two Plant Activators in Sunflower Plants
inferredcites →https://doi.org/10.1038/nri3141openalex-snapshot
How do plants achieve immunity? Defence without specialized immune cells
inferredcites →https://doi.org/10.1039/b100805fopenalex-snapshot
Probenazole - a plant defence activator
inferredcites →https://doi.org/10.1046/j.1365-2745.2000.00479.xopenalex-snapshot
Reduced growth and seed set following chemical induction of pathogen defence: does systemic acquired resistance (SAR) incur allocation costs?
inferredcites →https://doi.org/10.1046/j.1365-3059.2001.00609.xopenalex-snapshot
Production of pathogenesis‐related proteins in the cauliflower ( Brassica oleracea var. botrytis )–downy mildew ( Peronospora parasitica ) pathosystem treated with acibenzolar‐S‐methyl
inferredcites →https://doi.org/10.1046/j.1365-3059.2002.00754.xopenalex-snapshot
Induction of resistance in cocoa against Crinipellis perniciosa and Verticillium dahliae by acibenzolar‐ S ‐methyl (ASM)
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00952.xopenalex-snapshot
Probenazole induces systemic acquired resistance in Arabidopsis with a novel type of action
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01717.xopenalex-snapshot
Topology of the network integrating salicylate and jasmonate signal transduction derived from global expression phenotyping
inferredcites →https://doi.org/10.1046/j.1439-037x.2000.00419.xopenalex-snapshot
Effects of Salicylic Acid on the Development and Root Nodulation of Soybean Seedlings
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00646.xopenalex-snapshot
Beetle grazing reduces natural infection of Rumex obtusifolius by fungal pathogens
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00883.xopenalex-snapshot
Different signaling pathways of induced resistance by rhizobacteria in Arabidopsis thaliana against two pathovars of Pseudomonas syringae
inferredcites →https://doi.org/10.1055/s-2004-821176openalex-snapshot
Induction of Pathogen Resistance in Barley by Abiotic Stress
inferredcites →https://doi.org/10.1071/sr07109openalex-snapshot
Agronomic values of greenwaste biochar as a soil amendment
inferredcites →https://doi.org/10.1073/pnas.0504423102openalex-snapshot
The endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield
inferredcites →https://doi.org/10.1073/pnas.0510213103openalex-snapshot
Costs and benefits of priming for defense in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0708139104openalex-snapshot
Regulation of tradeoffs between plant defenses against pathogens with different lifestyles
inferredcites →https://doi.org/10.1078/1433-8319-00015openalex-snapshot
Induced systemic resistance (ISR) against pathogens – a promising field for ecological research
inferredcites →https://doi.org/10.1080/00021369.1973.10860764openalex-snapshot
Fate of 3-Allyloxy-1, 2-benzisothiazole 1, 1-Dioxide (Oryzemate®) in Rice Plants
inferredcites →https://doi.org/10.1086/417659openalex-snapshot
The Dilemma of Plants: To Grow or Defend
inferredcites →https://doi.org/10.1093/aob/mcl034openalex-snapshot
Rapid Accumulation of Trihydroxy Oxylipins and Resistance to the Bean Rust Pathogen Uromyces fabae Following Wounding in Vicia faba
inferredcites →https://doi.org/10.1093/aob/mcs055openalex-snapshot
Foliar aphid feeding recruits rhizosphere bacteria and primes plant immunity against pathogenic and non-pathogenic bacteria in pepper
inferredcites →https://doi.org/10.1093/jxb/ers046openalex-snapshot
Local and systemic mycorrhiza-induced protection against the ectoparasitic nematode Xiphinema index involves priming of defence gene responses in grapevine
inferredcites →https://doi.org/10.1093/jxb/ers100openalex-snapshot
The interaction of plant biotic and abiotic stresses: from genes to the field
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029397openalex-snapshot
Antagonistic Effect of Salicylic Acid and Jasmonic Acid on the Expression of Pathogenesis-Related (PR) Protein Genes in Wounded Mature Tobacco Leaves
inferredcites →https://doi.org/10.1093/pcp/pcm144openalex-snapshot
The Plant Growth-Promoting Fungus Penicillium simplicissimum GP17-2 Induces Resistance in Arabidopsis thaliana by Activation of Multiple Defense Signals
inferredcites →https://doi.org/10.1093/pcp/pcn147openalex-snapshot
Systemic Resistance in Arabidopsis Conferred by the Mycorrhizal Fungus Piriformospora indica Requires Jasmonic Acid Signaling and the Cytoplasmic Function of NPR1
inferredcites →https://doi.org/10.1094/mpmi-06-11-0177openalex-snapshot
Barley Leaf Transcriptome and Metabolite Analysis Reveals New Aspects of Compatibility and Piriformospora indica –Mediated Systemic Induced Resistance to Powdery Mildew
inferredcites →https://doi.org/10.1094/mpmi-18-0923openalex-snapshot
Signal Signature and Transcriptome Changes of Arabidopsis During Pathogen and Insect Attack
inferredcites →https://doi.org/10.1094/mpmi.1998.11.10.1017openalex-snapshot
Cell Defense Responses Associated with Localized and Systemic Resistance to Phytophthora parasitica Induced in Tomato by an Arbuscular Mycorrhizal Fungus
inferredcites →https://doi.org/10.1094/mpmi.1998.11.2.153openalex-snapshot
Involvement of Salicylic Acid in the Establishment of the Rhizobium meliloti-Alfalfa Symbiosis
inferredcites →https://doi.org/10.1094/mpmi.1999.12.11.1000openalex-snapshot
Mycorrhiza-Induced Changes in Disease Severity and PR Protein Expression in Tobacco Leaves
inferredcites →https://doi.org/10.1094/pdis-03-11-0183openalex-snapshot
Effect of Application Frequency and Reduced Rates of Acibenzolar-S-Methyl on the Field Efficacy of Induced Resistance Against Bacterial Spot on Tomato
inferredcites →https://doi.org/10.1094/pdis-08-10-0577openalex-snapshot
Cultivar Effects on the Expression of Induced Resistance in Spring Barley
inferredcites →https://doi.org/10.1094/pdis-10-10-0741openalex-snapshot
Effect of Biochar Amendments on Mycorrhizal Associations and Fusarium Crown and Root Rot of Asparagus in Replant Soils
inferredcites →https://doi.org/10.1094/pdis.2001.85.3.292openalex-snapshot
Management of Tomato spotted wilt virus in Flue-Cured Tobacco with Acibenzolar-S-Methyl and Imidacloprid
inferredcites →https://doi.org/10.1094/pdis.2001.85.8.879openalex-snapshot
Lack of Induced Systemic Resistance in Peanut to Late Leaf Spot Disease by Plant Growth-Promoting Rhizobacteria and Chemical Elicitors
inferredcites →https://doi.org/10.1094/pdis.2004.88.7.745openalex-snapshot
Lack of Control of Citrus Canker by Induced Systemic Resistance Compounds
inferredcites →https://doi.org/10.1094/phyto-08-11-0222openalex-snapshot
Induced Systemic Resistance in Arabidopsis thaliana Against Pseudomonas syringae pv. tomato by 2,4-Diacetylphloroglucinol-Producing Pseudomonas fluorescens
inferredcites →https://doi.org/10.1094/phyto-100-9-0913openalex-snapshot
Induction of Systemic Resistance in Plants by Biochar, a Soil-Applied Carbon Sequestering Agent
inferredcites →https://doi.org/10.1094/phyto-71-396openalex-snapshot
Effect of Energy-Requiring Defense Reactions on Yield and Grain Quality in a Powdery Mildew-Resistant Barley Cultivar
inferredcites →https://doi.org/10.1094/phyto-82-647openalex-snapshot
Lack of Effect of Tobacco Mosaic Virus-Induced Systemic Acquired Resistance on Arthropod Herbivores in Tobacco
inferredcites →https://doi.org/10.1094/phyto-86-498openalex-snapshot
Systemic Acquired Resistance and Susceptibility to Root-Knot Nematodes in Tomato
inferredcites →https://doi.org/10.1094/phyto-95-1368openalex-snapshot
Induced Resistance for Plant Disease Control: Maximizing the Efficacy of Resistance Elicitors
inferredcites →https://doi.org/10.1094/phyto-96-0181openalex-snapshot
The Molecular Biology of the Interactions Between Trichoderma spp., Phytopathogenic Fungi, and Plants
inferredcites →https://doi.org/10.1094/phyto.2004.94.2.171openalex-snapshot
Elicitors of Plant Defense Responses from Biocontrol Strains of Trichoderma viren
inferredcites →https://doi.org/10.1098/rsbl.2012.0416openalex-snapshot
Parents lend a helping hand to their offspring in plant defence
inferredcites →https://doi.org/10.1104/pp.111.187468openalex-snapshot
Next-Generation Systemic Acquired Resistance
inferredcites →https://doi.org/10.1104/pp.111.187831openalex-snapshot
Herbivory in the Previous Generation Primes Plants for Enhanced Insect Resistance
inferredcites →https://doi.org/10.1104/pp.111.191593openalex-snapshot
Descendants of Primed Arabidopsis Plants Exhibit Resistance to Biotic Stress
inferredcites →https://doi.org/10.1111/j.1364-3703.2010.00645.xopenalex-snapshot
Natural variation in priming of basal resistance: from evolutionary origin to agricultural exploitation
inferredcites →https://doi.org/10.1111/j.1364-3703.2010.00674.xopenalex-snapshot
The beneficial effect of Trichoderma spp. on tomato is modulated by the plant genotype
inferredcites →https://doi.org/10.1111/j.1364-3703.2011.00773.xopenalex-snapshot
The arbuscular mycorrhizal symbiosis promotes the systemic induction of regulatory defence‐related genes in rice leaves and confers resistance to pathogen infection
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Elicitation of foliar resistance mechanisms transiently impairs root association with arbuscular mycorrhizal fungi
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Whitefly infestation of pepper plants elicits defence responses against bacterial pathogens in leaves and roots and changes the below‐ground microflora
inferredcites →https://doi.org/10.1111/j.1365-3040.2004.01195.xopenalex-snapshot
Constitutive and induced resistance to pathogens in Arabidopsis thaliana depends on nitrogen supply
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Gene expression profiling and protection of Medicago truncatula against a fungal infection in response to an elicitor from green algae Ulva spp
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Effects of barley genotype on induced resistance to powdery mildew
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Effects of cucumber genotype on the induction of resistance to powdery mildew, Sphaerotheca fuliginea , by 2, 6‐dichloroisonicotinic acid
inferredcites →https://doi.org/10.1111/j.1365-3059.2005.01281.xopenalex-snapshot
Saccharin‐induced protection against powdery mildew in barley: effects on growth and phenylpropanoid metabolism
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Effects of host and pathogen genotypes on inducibility of resistance in tomato ( Solanum lycopersicum ) to Phytophthora infestans
inferredcites →https://doi.org/10.1111/j.1365-3059.2011.02471.xopenalex-snapshot
Phosphite primed defence responses and enhanced expression of defence genes in Arabidopsis thaliana infected with Phytophthora cinnamomi
inferredcites →https://doi.org/10.1111/j.1365-3059.2011.02493.xopenalex-snapshot
Silicon induced resistance against powdery mildew of roses caused by Podosphaera pannosa
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Induction of systemic resistance against Cucumber mosaic virus by Penicillium simplicissimum GP17‐2 in Arabidopsis and tobacco
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Arbuscular mycorrhizal symbiosis is accompanied by local and systemic alterations in gene expression and an increase in disease resistance in the shoots
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Trichoderma atroviride promotes growth and enhances systemic resistance to Diplodia pinea in radiata pine (Pinus radiata) seedlings
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Zusammenhänge zwischen streßinduzierten Veränderungen der Pathogenese von Erysiphe graminis hordei und Membrankomponenten der Gerste
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Induction of Disease Defensive Enzymes in Response to Treatment with acibenzolar‐S‐methyl (ASM) and Pseudomonas fluorescens Pf2 and Inoculation with Ralstonia solanacearum race 3, biovar 2 (phylotype II)
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Increased photosynthesis and resistance to rust infection in upper, uninfected leaves of rusted broad bean (Vicia faba L.)
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01439.xopenalex-snapshot
Induction of systemic protection against rust infection in broad bean by saccharin: effects on plant growth and development
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01602.xopenalex-snapshot
Mechanism of control of root‐feeding nematodes by mycorrhizal fungi in the dune grass Ammophila arenaria
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03987.xopenalex-snapshot
Treating seeds with activators of plant defence generates long‐lasting priming of resistance to pests and pathogens
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Effects of soil water level on the development of adult plant resistance to powdery mildew in barley
inferredcites →https://doi.org/10.1111/j.1744-7348.2011.00471.xopenalex-snapshot
The plant growth-promoting fungus Fusarium equiseti and the arbuscular mycorrhizal fungus Glomus mosseae stimulate plant growth and reduce severity of anthracnose and damping-off diseases in cucumber (Cucumis sativus) seedlings
inferredcites →https://doi.org/10.1139/b87-160openalex-snapshot
Effects of hardening and plant age on development of resistance to cottony snow mold (Coprinus psychromorbidus) in winter wheat under controlled conditions
inferredcites →https://doi.org/10.1146/annurev.phyto.22.1.53openalex-snapshot
The Interaction Between Environmental Stress Injury and Biotic Disease Physiology
inferredcites →https://doi.org/10.1146/annurev.phyto.41.052002.095505openalex-snapshot
Signal Crosstalk and Induced Resistance: Straddling the Line Between Cost and Benefit
inferredcites →https://doi.org/10.1155/2010/525291openalex-snapshot
Ulvan, a Sulfated Polysaccharide from Green Algae, Activates Plant Immunity through the Jasmonic Acid Signaling Pathway
inferredcites →https://doi.org/10.1584/jpestics.g10-94openalex-snapshot
Efficacy of probenazole for control of southern corn leaf blight
inferredcites →https://doi.org/10.1590/s0100-41582006000400007openalex-snapshot
Acibenzolar-S-Metil e Ecolife® na indução de respostas de defesa do tomateiro contra a mancha bacteriana (Xanthomonas vesicatoria)
inferredcites →https://doi.org/10.1590/s0103-90162000000100005openalex-snapshot
Ácido salicílico inibe a formação de micorrizas arbusculares e modifica a expressão de quitinases e b-1,3-glucanases em raízes de feijoeiro
inferredcites →https://doi.org/10.21273/horttech.15.3.0518openalex-snapshot
History and Perspectives on the Use of Disease Resistance Inducers in Horticultural Crops
inferredcites →https://doi.org/10.2134/agrojnl2007.0161openalex-snapshot
The Charcoal Vision: A Win–Win–Win Scenario for Simultaneously Producing Bioenergy, Permanently Sequestering Carbon, while Improving Soil and Water Quality
inferredcites →https://doi.org/10.23986/afsci.4997openalex-snapshot
Effects of AMF- and PGPR-root inoculation and a foliar chitosan spray in single and combined treatments on powdery mildew disease in strawberry
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/s12600-015-0461-6openalex-snapshot
Nursery treatments with non-conventional products against crown and root rot, caused by Phytophthora capsici, on zucchini
inferred← citeshttps://doi.org/10.1007/s12600-018-0644-zopenalex-snapshot
Management of late leaf spot (Phaeoisariopsis personata) and root rot (Macrophomina phaseolina) diseases of groundnut (Arachis hypogaea L.) with plant growth-promoting rhizobacteria, systemic acquired resistance inducers and plant extracts
inferred← citeshttps://doi.org/10.1007/s12600-019-00773-8openalex-snapshot
Evaluation of the effects of an eco-friendly crop protection system on management of whitefly-vectored chilli leaf curl virus disease in Sri Lanka
inferred← citeshttps://doi.org/10.1007/s12600-024-01234-7openalex-snapshot
A review of the use of phosphonates in the management of Phytophthora nicotianae in citrus in South Africa
inferred← citeshttps://doi.org/10.1007/s12600-025-01353-9openalex-snapshot
Plant essential oils in the management of Tuta absoluta (Meyrick): biological insights, classification, and mode of action
inferred← citeshttps://doi.org/10.1007/s13205-018-1501-yopenalex-snapshot
Lipopolysaccharide-induced priming enhances NO-mediated activation of defense responses in pearl millet challenged with Sclerospora graminicola
inferred← citeshttps://doi.org/10.1007/s13205-024-04040-4openalex-snapshot
Deciphering the defense response in tomato against Sclerotium rolfsii by Trichoderma asperellum strain A10 through gene expression analysis
inferred← citeshttps://doi.org/10.1007/s13313-017-0484-1openalex-snapshot
β– amino butyric acid mediated changes in cellular redox homeostasis confers tomato resistance to early blight
inferred← citeshttps://doi.org/10.1007/s13355-014-0319-2openalex-snapshot
Tomato treatment with chemical inducers reduces the performance of Spodoptera littoralis (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.1007/s13593-013-0158-5openalex-snapshot
Lettuce cropping with less pesticides. A review
inferred← citeshttps://doi.org/10.1007/s40415-017-0382-3openalex-snapshot
Activation of defense response in tomato against Fusarium wilt disease triggered by Trichoderma harzianum supplemented with exogenous chemical inducers (SA and MeJA)
inferred← citeshttps://doi.org/10.1007/s40626-016-0068-4openalex-snapshot
Improved resistance to disease and mites in strawberry, through the use of acibenzolar-S-methyl and harpin to enhance photosynthesis and phenolic metabolism
inferred← citeshttps://doi.org/10.1007/s40858-022-00508-xopenalex-snapshot
Inactivated bacterial suspension to control tomato bacterial spot
inferred← citeshttps://doi.org/10.1007/s41348-019-00222-yopenalex-snapshot
Weapons hidden underneath: bio-control agents and their potentials to activate plant induced systemic resistance in controlling crop Fusarium diseases
inferred← citeshttps://doi.org/10.1007/s41348-019-00290-0openalex-snapshot
Compost tea-mediated induction of resistance in biocontrol of strawberry Verticillium wilt
inferred← citeshttps://doi.org/10.1007/s41348-024-00878-1openalex-snapshot
Can biocontrol be the game-changer in integrated pest management? A review of definitions, methods and strategies
inferred← citeshttps://doi.org/10.1007/s41348-024-01017-6openalex-snapshot
Harnessing innate immunity: PR proteins expression in Malus domestica as an important defense mechanism against scab incited by Venturia inaequalis
inferred← citeshttps://doi.org/10.1007/s41348-025-01080-7openalex-snapshot
Microbial inoculants for plant resilience performance: roles, prospects and challenges
inferred← citeshttps://doi.org/10.1007/s42161-023-01322-3openalex-snapshot
Abiotic resistance inducers for management of bacterial wilt in tomato (Solanum lycopersicum L.)
inferred← citeshttps://doi.org/10.1007/s42161-024-01604-4openalex-snapshot
Soil amendments for management of Phytophthora root rot in avocado and their impact on the soil microbiome
inferred← citeshttps://doi.org/10.1007/s42161-024-01668-2openalex-snapshot
Salicylic acid blocks rice leaf blight by inhibiting biofilm formation of Xanthomonas oryzae pv. oryzae in rice
inferred← citeshttps://doi.org/10.1007/s42161-025-01914-1openalex-snapshot
Mushroom - derived antimicrobials – a source of eco-friendly antimicrobial compounds against phytopathogens
inferred← citeshttps://doi.org/10.1007/s42360-018-0072-5openalex-snapshot
Molecular recognition of fungal pathogens and activation of plant immune response
inferred← citeshttps://doi.org/10.1007/s42360-020-00203-4openalex-snapshot
Management of collar rot disease using vermicompost and a PGPR strain Pseudomonas sp. and their effect on defense-related enzymes in chickpea
inferred← citeshttps://doi.org/10.1007/s42360-020-00222-1openalex-snapshot
“Witches’ broom” disease of lime suppressed by some resistance inducers
inferred← citeshttps://doi.org/10.1007/s42360-023-00694-xopenalex-snapshot
Management of stem rot disease of groundnut (Arachis hypogaea) by alternate fungicides
inferred← citeshttps://doi.org/10.1007/s42398-020-00114-0openalex-snapshot
Elicitation of resistance through the exploration of acibenzolar-S-methyl (ASM) against Meloidogyne incognita in tomato under salt stress condition
inferred← citeshttps://doi.org/10.1007/s42729-021-00412-4openalex-snapshot
Mitigating Drought Stress in Sunflower (Helianthus annuus L.) Through Exogenous Application of β-Aminobutyric Acid
inferred← citeshttps://doi.org/10.1007/s44372-026-00580-6openalex-snapshot
Seed priming enhances physiological and biochemical adaptation of food crops to abiotic and biotic stresses under global warming
inferred← citeshttps://doi.org/10.1007/s44372-026-00837-0openalex-snapshot
Plant–microbe interactions as drivers of sustainable agriculture: molecular mechanisms, stress mitigation, and future prospects
inferred← citeshttps://doi.org/10.1016/b978-0-08-100596-5.00206-7openalex-snapshot
Natural Disease Control in Cereal Grains
inferred← citeshttps://doi.org/10.1016/b978-0-12-394437-5.00206-0openalex-snapshot
Natural Disease Control in Cereal Grains
inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00007-8openalex-snapshot
Vitamins and Environmental Stresses in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-817892-8.00001-5openalex-snapshot
Priming mediated stress and cross-stress tolerance in plants: Concepts and opportunities
inferred← citeshttps://doi.org/10.1016/b978-0-12-817892-8.00003-9openalex-snapshot
Getting ready with the priming: Innovative weapons against biotic and abiotic crop enemies in a global changing scenario
inferred← citeshttps://doi.org/10.1016/b978-0-12-818196-6.00006-6openalex-snapshot
Metabolomics in plant protection product research and development
inferred← citeshttps://doi.org/10.1016/b978-0-12-818258-1.00006-6openalex-snapshot
Microbial secondary metabolites and plant–microbe communications in the rhizosphere
inferred← citeshttps://doi.org/10.1016/b978-0-12-818469-1.00011-0openalex-snapshot
Signaling pathway of induced systemic resistance
inferred← citeshttps://doi.org/10.1016/b978-0-12-821843-3.00004-0openalex-snapshot
Principle, diversity, mechanism, and potential of practical application of plant probiotic bacteria for the biocontrol of phytopathogens by induced systemic resistance
inferred← citeshttps://doi.org/10.1016/b978-0-12-822122-8.00020-0openalex-snapshot
Friends in low places: Soil derived microbial inoculants for biostimulation and biocontrol in crop production
inferred← citeshttps://doi.org/10.1016/b978-0-323-85581-5.00017-3openalex-snapshot
Chitin and chitosan as elicitors in sustainable production of medicinal crops
inferred← citeshttps://doi.org/10.1016/b978-0-323-89871-3.00020-3openalex-snapshot
Biocontrol: a novel eco-friendly mitigation strategy to manage plant diseases
inferred← citeshttps://doi.org/10.1016/b978-0-323-90568-8.00005-5openalex-snapshot
Microbial elicitors: Positive and negative modulators of plant defense
inferred← citeshttps://doi.org/10.1016/b978-0-323-90587-9.00024-9openalex-snapshot
Resistance to geminivirus infections: natural and induced by controlled elicitation
inferred← citeshttps://doi.org/10.1016/b978-0-323-90620-3.00016-7openalex-snapshot
The potential of endophytes to sustain plant performance in a climate change scenario
inferred← citeshttps://doi.org/10.1016/b978-0-323-91005-7.00018-7openalex-snapshot
Mechanism and function of salicylate in plant toward biotic stress tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-323-91245-7.00021-3openalex-snapshot
Plant growth-promoting potential of endophytic bacteria for sustainable agriculture
inferred← citeshttps://doi.org/10.1016/b978-0-443-13365-7.00015-4openalex-snapshot
Microbial endophytes: prospects in biological control of plant pathogens and plant growth stimulation for sustainable agriculture
inferred← citeshttps://doi.org/10.1016/b978-0-443-15278-8.00002-4openalex-snapshot
Resistance: the phenotype
inferred← citeshttps://doi.org/10.1016/b978-0-443-21453-0.00008-7openalex-snapshot
Interaction of entomopathogenic fungi with the insects as plant disease vectors
inferred← citeshttps://doi.org/10.1016/b978-0-443-27324-7.00001-xopenalex-snapshot
Horticultural crops' biotic stresses in the present climatic scenario
inferred← citeshttps://doi.org/10.1016/b978-0-444-59576-8.00035-7openalex-snapshot
Enhanced Resistance of Plants to Disease Using Trichoderma spp.
inferred← citeshttps://doi.org/10.1016/b978-0-444-63504-4.00003-7openalex-snapshot
Role of Rhizobacterial Secondary Metabolites in Crop Protection Against Agricultural Pests and Diseases
inferred← citeshttps://doi.org/10.1016/bs.abr.2020.11.002openalex-snapshot
Plant metabolomics to the benefit of crop protection and growth stimulation
inferred← citeshttps://doi.org/10.1016/j.algal.2023.103063openalex-snapshot
Oligoalginates from Padina pavonica obtained by chemical and mechanical fractionation differentially induce resistance of date palm vitroplants to biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.bcab.2019.101279openalex-snapshot
Seed priming with biotic agents invokes defense response and enhances plant growth in pearl millet upon infection with Magnaporthe grisea
inferred← citeshttps://doi.org/10.1016/j.bcab.2021.101993openalex-snapshot
The stimulators and responsive genes to induce systemic resistance against pathogens: An exclusive focus on tomato as a model plant
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2015.10.014openalex-snapshot
Is induced systemic resistance the mechanism for control of black rot in Brassica oleracea by a Paenibacillus sp.?
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2015.11.001openalex-snapshot
Entomopathogenic nematodes induce systemic resistance in tomato against Spodoptera exigua, Bemisia tabaci and Pseudomonas syringae
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2022.105065openalex-snapshot
Disease resistance induction by K. marxianus against green mold in citrus via transcriptome analysis and verification based on metabolites
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2024.105690openalex-snapshot
Effective control of southern blight and root rot of Aconitum carmichaelii Debeaux by endophytic Bacillus velezensis YN-2-6S
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.carbpol.2021.118338openalex-snapshot
The non-sulfated ulvanobiuronic acid of ulvans is the smallest active unit able to induce an oxidative burst in dicot cells
inferred← citeshttps://doi.org/10.1016/j.carbpol.2023.121133openalex-snapshot
Spraying chitosan on cassava roots reduces postharvest deterioration by promoting wound healing and inducing disease resistance
inferred← citeshttps://doi.org/10.1016/j.coi.2019.12.001openalex-snapshot
Innate immunological memory: from plants to animals
inferred← citeshttps://doi.org/10.1016/j.coviro.2017.08.001openalex-snapshot
Manipulation of induced resistance to viruses
inferred← citeshttps://doi.org/10.1016/j.cropro.2014.07.015openalex-snapshot
COS-OGA: A novel oligosaccharidic elicitor that protects grapes and cucumbers against powdery mildew
inferred← citeshttps://doi.org/10.1016/j.cropro.2015.01.021openalex-snapshot
Management of leaf spot of wild rocket using fungicides, resistance inducers and a biocontrol agent, under greenhouse conditions
inferred← citeshttps://doi.org/10.1016/j.cropro.2015.08.021openalex-snapshot
Management of soil borne diseases of groundnut through seed dressing fungicides
inferred← citeshttps://doi.org/10.1016/j.cropro.2018.03.003openalex-snapshot
In-field assessment of an arabinoxylan polymer on disease control in spring barley
inferred← citeshttps://doi.org/10.1016/j.cropro.2018.12.014openalex-snapshot
Ulvan enhances seedling emergence and reduces Fusarium wilt severity in common bean (Phaseolus vulgaris L.)
inferred← citeshttps://doi.org/10.1016/j.cropro.2019.104967openalex-snapshot
Potential using of transgenerational resistance against common bacterial blight in Phaseolus vulgaris
inferred← citeshttps://doi.org/10.1016/j.cropro.2020.105446openalex-snapshot
Field management of Rotylenchulus reniformis on pineapple combining crop rotation, chemical-mediated induced resistance and endophytic bacterial inoculation
inferred← citeshttps://doi.org/10.1016/j.cropro.2021.105636openalex-snapshot
The potential of resistance inducers and synthetic fungicide combinations for management of foliar diseases of nursery stock
inferred← citeshttps://doi.org/10.1016/j.cropro.2026.107732openalex-snapshot
Post-invasion fungicide performance: Immediate interventions against coffee leaf rust (Hemileia vastatrix) in Hawaiʻian coffee production systems
inferred← citeshttps://doi.org/10.1016/j.cropro.2026.107900openalex-snapshot
Molecular background of elicitor-induced crop protection: A translational agronomic review
inferred← citeshttps://doi.org/10.1016/j.crsust.2021.100063openalex-snapshot
Biofertilizers: A Nexus between soil fertility and crop productivity under abiotic stress
inferred← citeshttps://doi.org/10.1016/j.dib.2024.110727openalex-snapshot
Transcriptomic dataset of Malus domestica young leaves in response to acibenzolar-S-methyl (ASM) and/or nitrogen nutrition
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.111817openalex-snapshot
Investigating the underlying mechanism of cadmium-induced plant adaptive response to genotoxic stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104124openalex-snapshot
Halotolerant plant growth–promoting bacteria: Prospects for alleviating salinity stress in plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106355openalex-snapshot
A plant-based biocontrol product confers protection against Phytophthora infestans and triggers tomato defense responses
inferred← citeshttps://doi.org/10.1016/j.envint.2019.02.066openalex-snapshot
In situ localization of micropollutants and associated stress response in Populus nigra leaves
inferred← citeshttps://doi.org/10.1016/j.envres.2022.114498openalex-snapshot
Warhorses in soil bioremediation: Seed biopriming with PGPF secretome to phytostimulate crop health under heavy metal stress
inferred← citeshttps://doi.org/10.1016/j.foodchem.2017.08.092openalex-snapshot
Yeast cell wall induces disease resistance against Penicillium expansum in pear fruit and the possible mechanisms involved
inferred← citeshttps://doi.org/10.1016/j.foodcont.2022.108996openalex-snapshot
Current situation and future challenges of patulin reduction-a review
inferred← citeshttps://doi.org/10.1016/j.funbio.2019.06.010openalex-snapshot
Trichoderma/pathogen/plant interaction in pre-harvest food security
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