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Fungicide resistance status in French populations of the wheat eyespot fungi Oculimacula acuformis and Oculimacula yallundae
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9063(199711)51:3<321::aid-ps639>3.0.co;2-uopenalex-snapshot
Evolution of fungicide resistance in the cereal eyespot fungiTapesia yallundaeandTapesia acuformisin France
inferredcites →https://doi.org/10.1002/(sici)1526-4998(200001)56:1<24::aid-ps71>3.0.co;2-yopenalex-snapshot
Functional diversity within the mitochondrial electron transport chain of plant pathogenic fungi
inferredcites →https://doi.org/10.1002/ps.1176openalex-snapshot
Metrafenone: studies on the mode of action of a novel cereal powdery mildew fungicide
inferredcites →https://doi.org/10.1002/ps.2028openalex-snapshot
Multiple mechanisms account for resistance to sterol 14α‐demethylation inhibitors in field isolates of Mycosphaerella graminicola
inferredcites →https://doi.org/10.1002/ps.2780430214openalex-snapshot
Mechanism of selectivity to fenpropimorph in Fusarium genus and Pseudocercosporella herpotrichoides
inferredcites →https://doi.org/10.1006/pest.1999.2406openalex-snapshot
Mutations of the β-Tubulin Gene Associated with Different Phenotypes of Benzimidazole Resistance in the Cereal Eyespot Fungi Tapesia yallundae and Tapesia acuformis
inferredcites →https://doi.org/10.1007/978-1-4020-2626-3_12openalex-snapshot
Chemical Control of Botrytis and its Resistance to Chemical Fungicides
inferredcites →https://doi.org/10.1007/978-94-010-0001-7_16openalex-snapshot
Secretion of natural and synthetic toxic compounds from filamentous fungi by membrane transporters of the ATP-binding cassette and major facilitator superfamily
inferredcites →https://doi.org/10.1016/0261-2194(94)90108-2openalex-snapshot
CGA 219417: a novel broad-spectrum fungicide
inferredcites →https://doi.org/10.1016/j.cropro.2010.02.019openalex-snapshot
Progress in understanding molecular mechanisms and evolution of resistance to succinate dehydrogenase inhibiting (SDHI) fungicides in phytopathogenic fungi
inferredcites →https://doi.org/10.1016/s0065-2296(00)33044-0openalex-snapshot
Pathogenicity, host-specificity, and population biology of tapesia spp., causal agents of eyespot disease of cereals
inferredcites →https://doi.org/10.1016/s0254-6299(15)30467-1openalex-snapshot
Revision of Pseudocercosporella-like species causing eyespot disease of wheat
inferredcites →https://doi.org/10.1016/s0378-1097(01)00066-0openalex-snapshot
Cloning of the CYP51 gene from the eyespot pathogen Tapesia yallundae indicates that resistance to the DMI fungicide prochloraz is not related to sequence changes in the gene encoding the target site enzyme
inferredcites →https://doi.org/10.1023/a:1008774821945openalex-snapshot
Resistance Risk Assessment of Cereal Eyespot, Tapesia Yallundae and Tapesia Acuformis, to the Anilinopyrimidine Fungicide, Cyprodinil
inferredcites →https://doi.org/10.1023/a:1020604716500openalex-snapshot
Secretion of Natural and Synthetic Toxic Compounds from Filamentous Fungi by Membrane Transporters of the ATP-binding Cassette and Major Facilitator Superfamily
inferredcites →https://doi.org/10.1023/a:1022584822191openalex-snapshot
Polymorphism of 14α-demethylase Gene (CYP51) in the Cereal Eyespot Fungi Tapesia acuformis and Tapesia yallundae
inferredcites →https://doi.org/10.1023/a:1026111030426openalex-snapshot
Eyespot of Cereals Revisited: ITS phylogeny Reveals New Species Relationships
inferredcites →https://doi.org/10.1051/agro:19880808openalex-snapshot
Caractérisation des souches de Pseudocercosporella herpotrichoides, agent du piétin-verse des céréales résistantes à des substances antimitotiques et à des inhibiteurs de la biosynthèse des stérols
inferredcites →https://doi.org/10.1051/agro:19910907openalex-snapshot
Caractérisation des souches de Pseudocercosporella herpotrichoides, agent du piétin-verse des céréales, résistantes au prochloraze, isolées en France sur blé tendre d'hiver
inferredcites →https://doi.org/10.1051/agro:19920301openalex-snapshot
Variabilité de Pseudocercosporella herpotrichoides (Fron) Deighton, agent du piétin-verse des céréales
inferredcites →https://doi.org/10.1094/phyto-60-1422openalex-snapshot
Metabolic Effects Related to Fungitoxicity of Carboxin
inferredcites →https://doi.org/10.1111/j.1365-3059.1985.tb01359.xopenalex-snapshot
Survey of benomyl resistance in Pseudocercosporella herpotrichoides on winter wheat and barley in England and Wales in 1983
inferredcites →https://doi.org/10.1111/j.1365-3059.1985.tb01375.xopenalex-snapshot
Morphology, benomyl resistance and pathogenicity to wheat and rye of isolates of Pseudocercosporella herpotrichoides
inferredcites →https://doi.org/10.1111/j.1365-3059.1988.tb02081.xopenalex-snapshot
Eyespot (Pseudocercosporella herpotrichoides) epidemiology in relation to prediction of disease severity and yield loss in winter wheat—a review
inferredcites →https://doi.org/10.1111/j.1365-3059.2007.01786.xopenalex-snapshot
Changes in fungicide sensitivity and relative species abundance in Oculimacula yallundae and O. acuformis populations (eyespot disease of cereals) in Western Europe
inferredcites →https://doi.org/10.1111/j.1439-0434.1966.tb02211.xopenalex-snapshot
Die Wirkungsweise von Cercosporella herpotrichoides Fron, dem Erreger der Halmbruchkrankheit des Getreides.
inferredcites →https://doi.org/10.1111/j.1744-7348.1974.tb01506.xopenalex-snapshot
Effects of eyespot on the yield of winter wheat
inferredcites →https://doi.org/10.1111/j.1744-7348.1990.tb04235.xopenalex-snapshot
Strategies for control of eyespot (Pseudocercosporella herpotrichoides) in UK winter wheat and winter barley
inferredcites →https://doi.org/10.1128/aem.00931-10openalex-snapshot
Exploring Mechanisms of Resistance to Respiratory Inhibitors in Field Strains of Botrytis cinerea , the Causal Agent of Gray Mold
inferredcites →https://doi.org/10.1128/aem.01332-10openalex-snapshot
Mechanism of Binding of Prothioconazole to Mycosphaerella graminicola CYP51 Differs from That of Other Azole Antifungals
inferredcites →https://doi.org/10.1128/aem.66.11.4599-4604.2000openalex-snapshot
Genetic Control of Resistance to the Sterol 14α-Demethylase Inhibitor Fungicide Prochloraz in the Cereal Eyespot Pathogen Tapesia yallundae
inferredcites →https://doi.org/10.1371/journal.ppat.1000696openalex-snapshot
Fungicide-Driven Evolution and Molecular Basis of Multidrug Resistance in Field Populations of the Grey Mould Fungus Botrytis cinerea
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Slipping Through the Cracks: Challenges and Prospects for Managing Fungal Pathogens Involved in Plant Disease Complexes
inferred← citeshttps://doi.org/10.1002/9783527644179.ch24openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527699261.ch16openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527699261.ch24openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ps.4361openalex-snapshot
Homozygous and heterozygous point mutations in succinate dehydrogenase subunits b, c and d of Rhizoctonia cerealis conferring resistance to thifluzamide
inferred← citeshttps://doi.org/10.1002/ps.5697openalex-snapshot
Antifungal activity of metyltetraprole against the existing QoI‐resistant isolates of various plant pathogenic fungi
inferred← citeshttps://doi.org/10.1002/ps.71340openalex-snapshot
In planta fluxapyroxad gradients from seed treatment differentially select fungicide‐sensitive and reduced‐sensitive genotypes of Pyrenophora teres f. maculata
inferred← citeshttps://doi.org/10.1002/ps.7726openalex-snapshot
Target and non‐target site mechanisms of fungicide resistance and their implications for the management of crop pathogens
inferred← citeshttps://doi.org/10.1007/978-4-431-55642-8_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-4-431-55642-8_14openalex-snapshot
Sterol Biosynthesis Inhibitors: C-4 Demethylation
inferred← citeshttps://doi.org/10.1007/978-4-431-55642-8_15openalex-snapshot
Multidrug Efflux Transporters
inferred← citeshttps://doi.org/10.1007/s10658-016-1082-8openalex-snapshot
Long-term dynamics of causative agents of stem base diseases in winter wheat and reaction of Czech Oculimacula spp. and Microdochium spp. populations to prochloraz
inferred← citeshttps://doi.org/10.1016/bs.aambs.2014.09.001openalex-snapshot
The Evolution of Fungicide Resistance
inferred← citeshttps://doi.org/10.1016/j.biortech.2023.130084openalex-snapshot
Functional screening pipeline to uncover laccase-like multicopper oxidase enzymes that transform industrial lignins
inferred← citeshttps://doi.org/10.1016/j.cropro.2024.106826openalex-snapshot
Slipping through the cracks: Challenges and prospects for investigating fungal plant disease complexes
inferred← citeshttps://doi.org/10.1016/j.hpj.2022.02.004openalex-snapshot
Fusarium wilt of banana: Current update and sustainable disease control using classical and essential oils approaches
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2020.108896openalex-snapshot
Multidrug resistance of Penicillium expansum to fungicides: whole transcriptome analysis of MDR strains reveals overexpression of efflux transporter genes
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105525openalex-snapshot
Multidrug resistance of Rhizoctonia solani determined by enhanced efflux for fungicides
inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106637openalex-snapshot
Phenotype MicroArray™ reveals the effects of azoxystrobin on the phenotypic characteristics of Rhizoctonia solani
inferred← citeshttps://doi.org/10.1016/j.tplants.2016.06.006openalex-snapshot
Trends and Challenges in Pesticide Resistance Detection
inferred← citeshttps://doi.org/10.1016/j.watres.2021.117775openalex-snapshot
Aqueous photodegradation of the benzophenone fungicide metrafenone: Carbon-bromine bond cleavage mechanism
inferred← citeshttps://doi.org/10.1038/srep04405openalex-snapshot
Effects of halving pesticide use on wheat production
inferred← citeshttps://doi.org/10.1071/fp15280openalex-snapshot
Chlorophyll fluorescence parameters allow the rapid detection and differentiation of plant responses in three different wheat pathosystems
inferred← citeshttps://doi.org/10.1088/1755-1315/1180/1/012033openalex-snapshot
Fungicide resistance of Fusarium oxysporum f.sp. cepae isolated from shallot in Brebes
inferred← citeshttps://doi.org/10.1094/pdis-01-16-0116-reopenalex-snapshot
Spatial and Temporal Sensitivity of Alternaria Species Associated With Potato Foliar Diseases to Demethylation Inhibiting and Anilino-Pyrimidine Fungicides
inferred← citeshttps://doi.org/10.1094/pdis-05-15-0574-feopenalex-snapshot
Toward a Reduced Reliance on Conventional Pesticides in European Agriculture
inferred← citeshttps://doi.org/10.1094/pdis-08-24-1701-reopenalex-snapshot
Multiple Single-Point Mutations in Stemphylium vesicarium Are Associated with the Rapid Development of Resistance to Succinate Dehydrogenase Inhibitors in Onion Fields
inferred← citeshttps://doi.org/10.1094/pdis-11-19-2457-reopenalex-snapshot
Evolution of the Resistance of Botrytis cinerea to Carbendazim and the Current Efficacy of Carbendazim Against Gray Mold After Long-Term Discontinuation
inferred← citeshttps://doi.org/10.1094/php-09-21-0118-rsopenalex-snapshot
Meta-Analysis of Yield Response to Applications of Fungicides Made at Different Crop Growth Stages in Michigan Winter Wheat
inferred← citeshttps://doi.org/10.1101/095869openalex-snapshot
Transcriptional study of the ABC transporter-encoding genes in response to fungicide treatment and during plant infection in the phytopathogenic fungus Botrytis cinerea
inferred← citeshttps://doi.org/10.1101/2023.12.27.573052openalex-snapshot
The Complex Landscape of Multidrug Resistance in Zymoseptoria tritici : MFS1 Promoter Plasticity and beyond
inferred← citeshttps://doi.org/10.1111/1462-2920.12781openalex-snapshot
Fungicide efflux and the MgMFS 1 transporter contribute to the multidrug resistance phenotype in Z ymoseptoria tritici field isolates
inferred← citeshttps://doi.org/10.1111/1462-2920.15760openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/mpp.12174openalex-snapshot
A pleiotropic drug resistance transporter is involved in reduced sensitivity to multiple fungicide classes in S clerotinia homoeocarpa ( F . T . B ennett)
inferred← citeshttps://doi.org/10.1111/ppa.12128openalex-snapshot
Constraints on the evolution of azole resistance in plant pathogenic fungi
inferred← citeshttps://doi.org/10.1111/ppa.13441openalex-snapshot
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inferred← citeshttps://doi.org/10.1128/msphere.00393-17openalex-snapshot
Plasticity of the MFS1 Promoter Leads to Multidrug Resistance in the Wheat Pathogen Zymoseptoria tritici
inferred← citeshttps://doi.org/10.1146/annurev-phyto-080417-050012openalex-snapshot
Fitness Penalties in the Evolution of Fungicide Resistance
inferred← citeshttps://doi.org/10.1371/journal.pone.0218569openalex-snapshot
Multiple mutations across the succinate dehydrogenase gene complex are associated with boscalid resistance in Didymella tanaceti in pyrethrum
inferred← citeshttps://doi.org/10.14199/ppp-2014-055openalex-snapshot
Fungicide resistance level of Oculimacula acuformis and O. yallundae isolates – the causal agents of eyespot
inferred← citeshttps://doi.org/10.1556/0806.46.2018.059openalex-snapshot
Reaction of eyespot causal agents to some active ingredients of fungicidesIn vitro
inferred← citeshttps://doi.org/10.17221/157/2016-ppsopenalex-snapshot
Resistance of winter wheat cultivars to eyespot and characterisation of causal agents of the disease
inferred← citeshttps://doi.org/10.17221/52/2019-cjgpbopenalex-snapshot
Reaction of winter wheat cultivars to eyespot assessed visually and by real-time PCR
inferred← citeshttps://doi.org/10.3186/jjphytopath.84.275openalex-snapshot
Distribution of Oculimacula yallundae and O. acuformis, causal fungi of wheat eyespot, their sensitivity to DMI fungicides, and control by DMIs in wheat fields of Hokkaido
inferred← citeshttps://doi.org/10.3389/fmicb.2017.00654openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants11111495openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants12061398openalex-snapshot
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