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The Fight against Plant-Parasitic Nematodes: Current Status of Bacterial and Fungal Biocontrol Agents

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In vivo infection of Bursaphelenchus xylophilus by the fungus Esteya vermicola
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Biological control of plant-parasitic nematodes : building coherence between microbial ecology and molecular mechanisms
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Regulation of Biological Control Agents
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Genomics and Molecular Genetics of Plant-Nematode Interactions
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Serratia sp., an endophyte of Mimosa pudica nodules with nematicidal, antifungal activity and growth-promoting characteristics
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The living strategy of nematophagous fungi
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Potential of Bacillus altitudinis KMS-6 as a biocontrol agent of Meloidogyne javanica
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inferredcites →https://doi.org/10.1007/s10658-019-01930-9openalex-snapshot
Hypothesized mechanism of biocontrol against pine wilt disease by the nematophagous fungus Esteya vermicola
inferredcites →https://doi.org/10.1007/s11248-012-9611-5openalex-snapshot
Transient expression of artificial microRNAs targeting Grapevine fanleaf virus and evidence for RNA silencing in grapevine somatic embryos
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Integration of Arbuscular Mycorrhizal and Nematode Antagonistic Fungi for the Biocontrol of Root Lesion Nematode Pratylenchus zeae Graham, 1951 on Sugarcane
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Biocontrol potential of nematophagous fungi against Meloidogyne spp. infecting tomato
inferredcites →https://doi.org/10.1007/s13213-019-01504-4openalex-snapshot
Bacillus halotolerans strain LYSX1-induced systemic resistance against the root-knot nematode Meloidogyne javanica in tomato
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Biological control of root-knot nematode on sugarcane in soil naturally or artificially infested with Pasteuria penetrans
inferredcites →https://doi.org/10.1007/s40858-019-00283-2openalex-snapshot
Biological control of the root-knot nematode Meloidogyne incognita on tomatoes and carrots by plant growth-promoting rhizobacteria
inferredcites →https://doi.org/10.1007/s42360-022-00498-5openalex-snapshot
Identification and potential utility of Metarhizium anisopliae (ITCC9014) for the management of root-knot nematode, Meloidogyne incognita
inferredcites →https://doi.org/10.1016/j.anres.2018.05.010openalex-snapshot
Nematophagous fungi: Far beyond the endoparasite, predator and ovicidal groups
inferredcites →https://doi.org/10.1016/j.apsoil.2003.07.001openalex-snapshot
Soil management to enhance bacterivore and fungivore nematode populations and their nitrogen mineralisation function
inferredcites →https://doi.org/10.1016/j.biocontrol.2017.07.010openalex-snapshot
Diversity and biocontrol potential of bacterial consortia associated to root-knot nematodes
inferredcites →https://doi.org/10.1016/j.biocontrol.2018.01.003openalex-snapshot
Suppression of root-knot disease in Pogostemon cablin caused by Meloidogyne incognita in a rhizobacteria mediated activation of phenylpropanoid pathway
inferredcites →https://doi.org/10.1016/j.biocontrol.2018.01.004openalex-snapshot
Isolation and identification of bacteria from rhizosphere soil and their effect on plant growth promotion and root-knot nematode disease
inferredcites →https://doi.org/10.1016/j.biocontrol.2018.07.018openalex-snapshot
Relative antagonistic potential of some rhizosphere biocontrol agents for the management of rice root-knot nematode, Meloidogyne graminicola
inferredcites →https://doi.org/10.1016/j.biocontrol.2018.09.003openalex-snapshot
Hyperparasitoids as new targets in biological control in a global change context
inferredcites →https://doi.org/10.1016/j.biocontrol.2019.104147openalex-snapshot
Evaluation of Bacillus aryabhattai Sneb517 for control of Heterodera glycines in soybean
inferredcites →https://doi.org/10.1016/j.biocontrol.2020.104185openalex-snapshot
Efficiency of Bacillus subtilis for root-knot and lesion nematodes management in sugarcane
inferredcites →https://doi.org/10.1016/j.biocontrol.2020.104425openalex-snapshot
Biological control of Pratylenchus brachyurus with isolates of Trichoderma spp. on soybean
inferredcites →https://doi.org/10.1016/j.biocontrol.2020.104445openalex-snapshot
The biocontrol potential of Pseudomonas fluorescens CHA0 against root knot nematode (Meloidogyne javanica) is dependent on the plant species
inferredcites →https://doi.org/10.1016/j.biocontrol.2021.104599openalex-snapshot
Isolation and characterization of streptomycetes and pseudomonad strains with antagonistic activity against the plant parasitic nematode Pratylenchus penetrans and fungi associated with replant disease
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Trichoderma harzianum induces resistance to root-knot nematodes by increasing secondary metabolite synthesis and defense-related enzyme activity in Solanum lycopersicum L
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Control potential of Meloidogyne javanica and Ditylenchus spp. using fluorescent Pseudomonas and Bacillus spp.
inferredcites →https://doi.org/10.1016/j.cropro.2018.02.009openalex-snapshot
Application methods of Steinernema feltiae, Xenorhabdus bovienii and Purpureocillium lilacinum to control root-knot nematodes in greenhouse tomato systems
inferredcites →https://doi.org/10.1016/j.cropro.2019.04.016openalex-snapshot
Beneficial bacterial volatile compounds for the control of root-knot nematode and bacterial leaf blight on rice
inferredcites →https://doi.org/10.1016/j.cropro.2020.105103openalex-snapshot
Assessment of rhizobacterial consortia to manage plant parasitic nematodes of grapevine
inferredcites →https://doi.org/10.1016/j.micres.2020.126613openalex-snapshot
Identification and characterization of Vietnamese coffee bacterial endophytes displaying in vitro antifungal and nematicidal activities
inferredcites →https://doi.org/10.1016/j.rhisph.2022.100528openalex-snapshot
Filtrates of mixed Bacillus spp inhibit second-stage juvenile motility of root-knot nematodes
inferredcites →https://doi.org/10.1016/j.scitotenv.2017.11.027openalex-snapshot
Pest management under climate change: The importance of understanding tritrophic relations
inferredcites →https://doi.org/10.1016/j.sjbs.2021.07.081openalex-snapshot
Management of root-knot nematode, Meloidogyne incognita and soil borne fungus, Fusarium oxysporum in cucumber using three bioagents under polyhouse conditions
inferredcites →https://doi.org/10.1016/j.ympev.2017.07.027openalex-snapshot
Molecular characterization and species delimiting of plant-parasitic nematodes of the genus Pratylenchus from the penetrans group (Nematoda: Pratylenchidae)
inferredcites →https://doi.org/10.1017/s0953756298006984openalex-snapshot
Esteya, a new nematophagous genus from Taiwan, attacking the pinewood nematode (Bursaphelenchus xylophilus)
inferredcites →https://doi.org/10.1021/acs.jafc.1c05454openalex-snapshot
Uncovering Nematicidal Natural Products from Xenorhabdus Bacteria
inferredcites →https://doi.org/10.1038/nature13855openalex-snapshot
Belowground biodiversity and ecosystem functioning
inferredcites →https://doi.org/10.1038/s41598-019-47942-7openalex-snapshot
Bacteria isolated from the cuticle of plant-parasitic nematodes attached to and antagonized the root-knot nematode Meloidogyne hapla
inferredcites →https://doi.org/10.1038/s41598-019-48739-4openalex-snapshot
Distribution and diversity of bacterial endophytes from four Pinus species and their efficacy as biocontrol agents for devastating pine wood nematodes
inferredcites →https://doi.org/10.1038/s41598-020-65262-zopenalex-snapshot
In vitro evaluation of Penicillium chrysogenum Snef1216 against Meloidogyne incognita (root-knot nematode)
inferredcites →https://doi.org/10.1038/s41598-021-93567-0openalex-snapshot
Bacillus firmus I-1582 promotes plant growth and impairs infection and development of the cyst nematode Heterodera schachtii over two generations
inferredcites →https://doi.org/10.1073/pnas.0538072100openalex-snapshot
Bacillus thuringiensis crystal proteins that target nematodes
inferredcites →https://doi.org/10.1073/pnas.1007276107openalex-snapshot
A Trojan horse mechanism of bacterial pathogenesis against nematodes
inferredcites →https://doi.org/10.1079/9780851997278.0000openalex-snapshot
Plant parasitic nematodes in subtropical and tropical agriculture
inferredcites →https://doi.org/10.1079/9781780641515.0000openalex-snapshot
Plant nematology
inferredcites →https://doi.org/10.1079/9781789247541.0000openalex-snapshot
Integrated nematode management: state-of-the-art and visions for the future
inferredcites →https://doi.org/10.1080/03235408.2020.1820169openalex-snapshot
Association of root-knot nematode (Meloidogyne javanica) in olive plantations in Rajasthan (India) and its natural suppression by Pasteuria penetrans
inferredcites →https://doi.org/10.1080/03235408.2021.1925501openalex-snapshot
Bacillus is one of the most potential genus as a biocontrol agent of golden cyst nematode (Globodera rostochiensis)
inferredcites →https://doi.org/10.1080/07060661.2021.1910345openalex-snapshot
Ditylenchus dipsaci and Fusarium oxysporum on garlic: one plus one does not equal two
inferredcites →https://doi.org/10.1080/09583157.2018.1441369openalex-snapshot
Using the nematophagous fungus Esteya vermicola to control the disastrous pine wilt disease
inferredcites →https://doi.org/10.1080/09583157.2020.1765980openalex-snapshot
Role of bacterial antagonists of fungal pathogens, Bacillus thuringiensis KYC and Bacillus velezensis CE 100 in control of root-knot nematode, Meloidogyne incognita and subsequent growth promotion of tomato
inferredcites →https://doi.org/10.1080/09583157.2020.1833304openalex-snapshot
Arbuscular mycorrhizal fungi against the false root-knot nematode activity inCapsicum annuum: physiological responses in plants
inferredcites →https://doi.org/10.1093/femsle/fnz169openalex-snapshot
Nematicidal metabolites from endophytic fungus Chaetomium globosum YSC5
inferredcites →https://doi.org/10.1094/pdis-06-21-1139-reopenalex-snapshot
Bacterial Volatile-Mediated Suppression of Root-Knot Nematode ( Meloidogyne incognita )
inferredcites →https://doi.org/10.1094/pdis-09-17-1392-reopenalex-snapshot
Suppression of Meloidogyne incognita by the Entomopathogenic Fungus Lecanicillium muscarium
inferredcites →https://doi.org/10.1094/pdis-12-10-0902openalex-snapshot
Detection of Bursaphelenchus Xylophilus , Causal Agent of Pine Wilt Disease on Pinus pinaster in Northwestern Spain
inferredcites →https://doi.org/10.1094/php-10-20-0094-bropenalex-snapshot
Known Distribution of the Soybean Cyst Nematode, Heterodera glycines, in the United States and Canada in 2020
inferredcites →https://doi.org/10.1094/phyto-01-13-0019-rvwopenalex-snapshot
Major Emerging Problems with Minor Meloidogyne Species
inferredcites →https://doi.org/10.1094/phyto-05-12-0114-ropenalex-snapshot
Small Subunit Ribosomal DNA-Based Phylogenetic Analysis of Foliar Nematodes (Aphelenchoidesspp.) and Their Quantitative Detection in Complex DNA Backgrounds
inferredcites →https://doi.org/10.1094/phyto-06-20-0229-ropenalex-snapshot
Esteya floridanum sp. nov.: An Ophiostomatalean Nematophagous Fungus and Its Potential to Control the Pine Wood Nematode
inferredcites →https://doi.org/10.1094/phyto-84-294openalex-snapshot
Use of Species-Specific Satellite DNA fromBursaphelenchus xylophilusas a Diagnostic Probe
inferredcites →https://doi.org/10.1111/aab.12105openalex-snapshot
Molecular biology of root lesion nematodes ( Pratylenchus spp.) and their interaction with host plants
inferredcites →https://doi.org/10.1111/eea.12807openalex-snapshot
The implications of rapid eco‐evolutionary processes for biological control ‐ a review
inferredcites →https://doi.org/10.1111/efp.12745openalex-snapshot
Isolation and identification of Esteya vermicola and its potential for controlling pinewood nematode
inferredcites →https://doi.org/10.1111/eva.12750openalex-snapshot
Rapid change in host specificity in a field population of the biological control organism Pasteuria penetrans
inferredcites →https://doi.org/10.1111/eva.13001openalex-snapshot
Natural variation of root lesion nematode antagonism in the biocontrol fungus Clonostachys rosea and identification of biocontrol factors through genome‐wide association mapping
inferredcites →https://doi.org/10.1111/eva.13457openalex-snapshot
Biological control needs evolutionary perspectives of ecological interactions
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Population decline of potato cyst nematodes (Globodera rostochiensis, G. pallida) in field soils in Northern Ireland
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Impact of nematodes on grapevine growth and productivity: current knowledge and future directions, with special reference to Australian viticulture
inferredcites →https://doi.org/10.1111/jph.12755openalex-snapshot
Biological control of Pratylenchus brachyurus in soya bean crops
inferredcites →https://doi.org/10.1111/mpp.12057openalex-snapshot
Top 10 plant‐parasitic nematodes in molecular plant pathology
inferredcites →https://doi.org/10.1128/microbiolspec.funk-0022-2016openalex-snapshot
Nematode-Trapping Fungi
inferredcites →https://doi.org/10.1146/annurev-phyto-080614-120336openalex-snapshot
Molecular Mechanisms of Nematode-Nematophagous Microbe Interactions: Basis for Biological Control of Plant-Parasitic Nematodes
inferredcites →https://doi.org/10.1146/annurev.py.21.090183.001221openalex-snapshot
Pathology of the Pine Wilt Disease Caused by Bursaphelenchus xylophilus
inferredcites →https://doi.org/10.11519/jjfs1953.51.7_193openalex-snapshot
Bursaphelenchus sp. in the wood of dead pine trees
inferredcites →https://doi.org/10.1163/138855411x587112openalex-snapshot
An evaluation of the implications of virulence in non-European populations of Globodera pallida and G. rostochiensis for potato cultivation in Europe
inferredcites →https://doi.org/10.1163/156854106778613958openalex-snapshot
Molecular and morphological consilience in the characterisation and delimitation of five nematode species from Florida belonging to the Xiphinema americanum-group
inferredcites →https://doi.org/10.1163/15685411-bja10064openalex-snapshot
Fungal biocontrol reduces the populations of the lesion nematode, Pratylenchus brachyurus, in soybean and corn
inferredcites →https://doi.org/10.1163/156854199508757openalex-snapshot
First report of Bursaphelenchus xylophilus in Portugal and in Europe
inferredcites →https://doi.org/10.1163/187529264x00574openalex-snapshot
Factors Affecting the Control of Eelworm Diseases 1)
inferredcites →https://doi.org/10.1163/187529286x00345openalex-snapshot
Variation Between Strains of the Nematophagous Fungus, Verticillium Chlamydosporium Goddard. Ii. Factors Affecting Parasitism of Cyst Nematode Eggs
inferredcites →https://doi.org/10.1163/9789004387584openalex-snapshot
Systematics of Root-knot Nematodes (Nematoda: Meloidogynidae)
inferredcites →https://doi.org/10.1163/ej.9789004155640.i-523openalex-snapshot
Pratylenchus (Nematoda: Pratylenchidae): Diagnosis, Biology, Pathogenicity and Management
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An update on the genus Longidorus, Paralongidorus and Xiphinema (Family Longidoridae) in Portugal
inferredcites →https://doi.org/10.1186/s12866-021-02385-xopenalex-snapshot
A new strain of Volutella citrinella with nematode predation and nematicidal activity, isolated from the cysts of potato cyst nematodes in China
inferredcites →https://doi.org/10.1186/s13568-019-0894-2openalex-snapshot
Nematicidal potential of Streptomyces antibioticus strain M7 against Meloidogyne incognita
inferredcites →https://doi.org/10.1186/s41938-017-0011-2openalex-snapshot
Comparative effects of entomopathogenic fungi and nematodes and bacterial supernatants against rice white tip nematode
inferredcites →https://doi.org/10.1186/s41938-021-00383-9openalex-snapshot
Biocontrol potential of bacterial isolates from vermicompost and earthworm against the root-knot nematode Meloidogyne javanica infecting tomato plants
inferredcites →https://doi.org/10.13057/biodiv/d211032openalex-snapshot
Consortium of endophytic bacteria and rhizobacteria effectively suppresses the population of Pratylenchus coffeae and promotes the growth of Robusta coffee
inferredcites →https://doi.org/10.1371/journal.pone.0213230openalex-snapshot
Bio-control agents activate plant immune response and prime susceptible tomato against root-knot nematodes
inferredcites →https://doi.org/10.1371/journal.pone.0232770openalex-snapshot
Colonization of Beauveria bassiana 08F04 in root-zone soil and its biocontrol of cereal cyst nematode (Heterodera filipjevi)
inferredcites →https://doi.org/10.14601/phytopathol_mediterr-23780openalex-snapshot
An integrative approach for the selection of Pochonia chlamydosporia isolates for biocontrol of potato cyst and root knot nematodes
inferredcites →https://doi.org/10.15666/aeer/1801_11291140openalex-snapshot
EFFECT OF CULTURE FILTRATE OF SINORHIZOBIUM FREDIISNEB183 ON THE ACTIVITY AND BEHAVIOR OF SOYBEAN CYST NEMATODE (HETERODERA GLYCINES ICHINOHE, 1952)
inferredcites →https://doi.org/10.1590/1983-21252019v32n105rcopenalex-snapshot
BIOLOGICAL MANAGEMENT OF Pratylenchus brachyurus IN SOYBEAN CROPS
inferredcites →https://doi.org/10.17921/1415-6938.2021v25n5-esp.p783-787openalex-snapshot
Extrato de Pycnoporus sanguineus no Controle de Meloidogyne javanica em Tomateiro
inferredcites →https://doi.org/10.18681/pjn.v36.i01.p71-81openalex-snapshot
Seasonal fluctuation and biological control of root- knot nematodes Meloidogyne incognita on cucumber
inferredcites →https://doi.org/10.18681/pjn.v36.i02.p163-176openalex-snapshot
Bio-control potential of Bacillus isolates against cereal cyst nematode (Heterodera avenae)
inferredcites →https://doi.org/10.18681/pjn.v37.i01.p53-61openalex-snapshot
Bacillus cereus a potential strain infested cereal cyst nematode (Heterodera avenae)
inferredcites →https://doi.org/10.21307/jofnem-2020-070openalex-snapshot
Compatibility of fluazaindolizine and oxamyl with Pasteuria penetrans on spore attachment to juveniles of Meloidogyne javanica and M. incognita
inferredcites →https://doi.org/10.2134/agronj2018.05.0314openalex-snapshot
Soybean Cyst Nematode Control with Pasteuria nishizawae Under Different Management Practices
inferredcites →https://doi.org/10.21548/33-1-1302openalex-snapshot
Xiphinema index and its Relationship to Grapevines: A review
inferredcites →https://doi.org/10.2478/s11687-012-0020-3openalex-snapshot
The pinewood nematode, Bursaphelenchus xylophilus, in Madeira Island
inferredcites →https://doi.org/10.2478/s11687-013-0133-3openalex-snapshot
Morphological characterisation and diagnostics of Xiphinema non-americanum group species (Nematoda: Longidoridae) from Romania using mutiplex PCR
inferredcites →https://doi.org/10.33448/rsd-v10i6.15132openalex-snapshot
Use of the Glomus etunicatum as biocontrol agent of the soybean cyst nematode
inferredcites →https://doi.org/10.3389/ffunb.2022.863198openalex-snapshot
Strategy of Nematophagous Fungi in Determining the Activity of Plant Parasitic Nematodes and Their Prospective Role in Sustainable Agriculture
inferredcites →https://doi.org/10.3389/fmicb.2015.01280openalex-snapshot
Arbuscular Mycorrhizal Fungi for the Biocontrol of Plant-Parasitic Nematodes: A Review of the Mechanisms Involved
inferredcites →https://doi.org/10.3389/fmicb.2019.03042openalex-snapshot
Commercial Formulates of Trichoderma Induce Systemic Plant Resistance to Meloidogyne incognita in Tomato and the Effect Is Additive to That of the Mi-1.2 Resistance Gene
inferredcites →https://doi.org/10.3389/fmicb.2020.00313openalex-snapshot
Plants and Associated Soil Microbiota Cooperatively Suppress Plant-Parasitic Nematodes
inferredcites →https://doi.org/10.3389/fmicb.2022.843041openalex-snapshot
The Biocontrol Functions of Bacillus velezensis Strain Bv-25 Against Meloidogyne incognita
inferredcites →https://doi.org/10.3389/fmicb.2022.915546openalex-snapshot
Nematicidal Activity of Burkholderia arboris J211 Against Meloidogyne incognita on Tobacco
inferredcites →https://doi.org/10.3389/fpls.2019.00945openalex-snapshot
Pochonia chlamydosporia Induces Plant-Dependent Systemic Resistance to Meloidogyne incognita
inferredcites →https://doi.org/10.3389/fpls.2020.00796openalex-snapshot
Bacillus firmus Strain I-1582, a Nematode Antagonist by Itself and Through the Plant
inferredcites →https://doi.org/10.3389/fpls.2022.908308openalex-snapshot
Fungal Communities of the Pine Wilt Disease Complex: Studying the Interaction of Ophiostomatales With Bursaphelenchus xylophilus
inferredcites →https://doi.org/10.3390/agronomy10081148openalex-snapshot
Global Research on Plant Nematodes
inferredcites →https://doi.org/10.3390/agronomy12071508openalex-snapshot
Effect of Molasses Application Alone or Combined with Trichoderma asperellum T-34 on Meloidogyne spp. Management and Soil Microbial Activity in Organic Production Systems
inferredcites →https://doi.org/10.3390/horticulturae8030208openalex-snapshot
Top Ten Most Important U.S.-Regulated and Emerging Plant-Parasitic Nematodes
inferredcites →https://doi.org/10.3390/insects9040131openalex-snapshot
An Alternative Perspective for the Theory of Biological Control
inferredcites →https://doi.org/10.3390/jof7090780openalex-snapshot
Insights into the Role of Fungi in Pine Wilt Disease
inferredcites →https://doi.org/10.3390/microorganisms10010168openalex-snapshot
The Potential of Esteya spp. for the Biocontrol of the Pinewood Nematode, Bursaphelenchus xylophilus
inferredcites →https://doi.org/10.3390/microorganisms10071266openalex-snapshot
Roles of Arbuscular mycorrhizal Fungi as a Biocontrol Agent in the Control of Plant Diseases
inferredcites →https://doi.org/10.3390/microorganisms10071343openalex-snapshot
Identification of Nematicidal Metabolites from Purpureocillium lavendulum
inferredcites →https://doi.org/10.3390/microorganisms9112268openalex-snapshot
Pathogenicity and Volatile Nematicidal Metabolites from Duddingtonia flagrans against Meloidogyne incognita
inferredcites →https://doi.org/10.3390/pathogens7040076openalex-snapshot
Effect of Arbuscular Mycorrhizal Fungi on Pratylenchus penetrans Infestation in Apple Seedlings under Greenhouse Conditions
inferredcites →https://doi.org/10.3390/plants10010168openalex-snapshot
Morphological and Molecular Characterization of Pratylenchus dakotaensis n. sp. (Nematoda: Pratylenchidae), a New Root-Lesion Nematode Species on Soybean in North Dakota, USA
inferredcites →https://doi.org/10.3390/plants10020389openalex-snapshot
Bacteria as Biocontrol Tool against Phytoparasitic Nematodes
inferredcites →https://doi.org/10.3390/plants10040718openalex-snapshot
Root Endophytism by Pochonia chlamydosporia Affects Defense-Gene Expression in Leaves of Monocot and Dicot Hosts under Multiple Biotic Interactions
inferredcites →https://doi.org/10.3390/plants10122655openalex-snapshot
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inferredcites →https://doi.org/10.3390/plants11030275openalex-snapshot
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inferredcites →https://doi.org/10.3390/plants9091167openalex-snapshot
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inferredcites →https://doi.org/10.3897/mycokeys.33.23341openalex-snapshot
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inferredcites →https://doi.org/10.4038/josuk.v13i0.8021openalex-snapshot
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inferredcites →https://doi.org/10.7202/1046783aropenalex-snapshot
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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/s10340-024-01815-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10343-026-01389-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118937openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pt.2025.04.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jafc.3c06074openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d4va00216dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1079/9781800625228.0008openalex-snapshot
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inferred← citeshttps://doi.org/10.1079/9781836990413.0021openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jambio/lxae111openalex-snapshot
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inferred← citeshttps://doi.org/10.1094/pdis-09-25-2002-reopenalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jph.70201openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jph.70290openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jph.70323openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/nph.70125openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12864-025-12175-8openalex-snapshot
Identification and functional characterization of the histone acetyltransferase gene family in Bursaphelenchus xylophilus
inferred← citeshttps://doi.org/10.1186/s42483-025-00395-5openalex-snapshot
Plant disease complexes: Xanthomonas co-infections with multiple pathogens
inferred← citeshttps://doi.org/10.1371/journal.pone.0295945openalex-snapshot
The nematicide emamectin benzoate increases ROS accumulation in Pinus massoniana and poison Monochamus alternatus
inferred← citeshttps://doi.org/10.14295/bjs.v6i2.939openalex-snapshot
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inferred← citeshttps://doi.org/10.14720/aas.2023.119.4.15212openalex-snapshot
Možnosti nekemičnega zatiranja virusonosnih ogorčic Xiphinema index Thorne & Allen, 1950
inferred← citeshttps://doi.org/10.16970/entoted.1667614openalex-snapshot
Optimization of a Bacillus-based bioproduct for Meloidogyne incognita (Kofoid & White, 1919) Chitwood, 1949 (Tylenchida: Meloidogynidae) control using response surface methodology
inferred← citeshttps://doi.org/10.17221/5/2025-ppsopenalex-snapshot
Interaction of seaweed metabolites with plants to enhance protection against biotic and abiotic stresses
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2379103/v1openalex-snapshot
Bacteria from the Sonoran Desert with nematicidal potential against phytopathogenic nematodes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4799842/v1openalex-snapshot
The extract of Hypoxylon spp. Sj18 kills the pinewood nematode through nematode-associated bacteria
inferred← citeshttps://doi.org/10.2139/ssrn.5014979openalex-snapshot
Glycine Max Sec61 Complex Genes as They Relate to a Soybean Defense Response to the Parasitic Nematode Heterodera Glycines
inferred← citeshttps://doi.org/10.2174/0118743315443780260114110802openalex-snapshot
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inferred← citeshttps://doi.org/10.29133/yyutbd.1666297openalex-snapshot
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inferred← citeshttps://doi.org/10.32404/rean.v10i3.7725openalex-snapshot
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inferred← citeshttps://doi.org/10.33448/rsd-v12i4.40989openalex-snapshot
Nematicidal activity of Brazilian honeys
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1210288openalex-snapshot
Function discovery of a non-ribosomal peptide synthetase-like encoding gene in the nematode-trapping fungus Arthrobotrys oligospora
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1213306openalex-snapshot
Native Bacillus paralicheniformis isolate as a potential agent for phytopathogenic nematodes control
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1404439openalex-snapshot
Insights into the efficient degradation mechanism of extracellular proteases mediated by Purpureocillium lilacinum
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1433716openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2024.1455880openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphar.2024.1508835openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2023.1230968openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2023.1257744openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2025.1602326openalex-snapshot
Effect of botanicals, organic nutrient sources, and bio-control agents on root-knot nematode (Meloidogyne incognita) infecting tomato
inferred← citeshttps://doi.org/10.3389/fpls.2026.1867596openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/agriculture16080860openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/agrochemicals5010013openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/cells12040543openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/horticulturae10040407openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25126300openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25126435openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25147680openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms252010934openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jof9020206openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jof9121125openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jof9121183openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms10112274openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms13061215openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms13061337openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms14081676openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules29194673openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules30020411openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules30091946openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules30112453openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/pathogens12091114openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants12020382openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants12030521openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants12244104openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants13182634openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants14020269openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants14050754openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants14101420openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/su151411421openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/toxins14120849openalex-snapshot
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inferred← citeshttps://doi.org/10.4014/jmb.2602.02003openalex-snapshot
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inferred← citeshttps://doi.org/10.4236/as.2023.1411098openalex-snapshot
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inferred← citeshttps://doi.org/10.53859/02352451_2026_40_7_33openalex-snapshot
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inferred← citeshttps://doi.org/10.55627/pbiotech.001.01.0665openalex-snapshot
Computational analysis of 16D10 effector peptides from root-knot nematodes and their interaction with Mi resistance (R) protein through molecular docking
inferred← citeshttps://doi.org/10.55905/rdelosv16.n45-009openalex-snapshot
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inferred← citeshttps://doi.org/10.5772/intechopen.1002237openalex-snapshot
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inferred← citeshttps://doi.org/10.5772/intechopen.110977openalex-snapshot
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inferred← citeshttps://doi.org/10.7769/gesec.v15i1.3343openalex-snapshot
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