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Metabolic Capacity Differentiates Plenodomus lingam from P. biglobosus Subclade ‘brassicae’, the Causal Agents of Phoma Leaf Spotting and Stem Canker of Oilseed Rape (Brassica napus) in Agricultural Ecosystems
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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/ps.1890openalex-snapshot
Effects of fungicides on in vitro spore germination and mycelial growth of the phytopathogens Leptosphaeria maculans and L. biglobosa (phoma stem canker of oilseed rape)
inferredcites →https://doi.org/10.1006/fgbi.2001.1274openalex-snapshot
Leptosphaeria maculans, the Causal Agent of Blackleg Disease of Brassicas
inferredcites →https://doi.org/10.1007/bf00355054openalex-snapshot
Electrophoretic karyotyping of Leptosphaeria maculans differentiates highly virulent from weakly virulent isolates
inferredcites →https://doi.org/10.1007/bf03195702openalex-snapshot
Analyses of air samples for ascospores ofLeptosphaeria maculans andL.biglobosa by light microscopy and molecular techniques
inferredcites →https://doi.org/10.1007/s00122-008-0844-xopenalex-snapshot
Molecular and phenotypic characterization of near isogenic lines at QTL for quantitative resistance to Leptosphaeria maculans in oilseed rape (Brassica napus L.)
inferredcites →https://doi.org/10.1007/s00122-018-3103-9openalex-snapshot
Multi-year linkage and association mapping confirm the high number of genomic regions involved in oilseed rape quantitative resistance to blackleg
inferredcites →https://doi.org/10.1007/s00217-018-3125-1openalex-snapshot
Quality assessment of goji fruits, cranberries, and raisins using selected markers
inferredcites →https://doi.org/10.1007/s00294-004-0539-zopenalex-snapshot
Identification and characterization of polymorphic minisatellites in the phytopathogenic ascomycete Leptosphaeria maculans
inferredcites →https://doi.org/10.1007/s10453-015-9404-4openalex-snapshot
Effect of climate change on sporulation of the teleomorphs of Leptosphaeria species causing stem canker of brassicas
inferredcites →https://doi.org/10.1007/s10658-005-2233-5openalex-snapshot
World-Wide Importance of Phoma Stem Canker (Leptosphaeria maculans and L. biglobosa) on Oilseed Rape (Brassica napus)
inferredcites →https://doi.org/10.1007/s10658-005-2931-zopenalex-snapshot
Frequency of Avirulence Alleles in Field Populations of Leptosphaeria maculans in Europe
inferredcites →https://doi.org/10.1007/s10658-005-3479-7openalex-snapshot
Durability of Resistance and Cost of Virulence
inferredcites →https://doi.org/10.1007/s10658-014-0513-7openalex-snapshot
Phoma stem canker disease on oilseed rape (Brassica napus) in China is caused by Leptosphaeria biglobosa ‘brassicae’
inferredcites →https://doi.org/10.1007/s10658-015-0819-0openalex-snapshot
Breakdown of Rlm3 resistance in the Brassica napus–Leptosphaeria maculans pathosystem in western Canada
inferredcites →https://doi.org/10.1007/s10658-016-0922-xopenalex-snapshot
Monitoring blackleg (Leptosphaeria spp.) ascospore release timing and quantity enables optimal fungicide application to improved oilseed rape yield and seed quality
inferredcites →https://doi.org/10.1007/s10658-021-02428-zopenalex-snapshot
Detection of the Phoma pathogens Plenodomus biglobosus subclades ‘brassicae’ and ‘canadensis’ on wasabi, and ‘canadensis’ in Europe
inferredcites →https://doi.org/10.1007/s13353-014-0235-8openalex-snapshot
Molecular screening for avirulence alleles AvrLm1 and AvrLm6 in airborne inoculum of Leptosphaeria maculans and winter oilseed rape (Brassica napus) plants from Poland and the UK
inferredcites →https://doi.org/10.1016/j.fcr.2014.06.023openalex-snapshot
Breakdown of resistance to the fungal disease, blackleg, is averted in commercial canola (Brassica napus) crops in Australia
inferredcites →https://doi.org/10.1016/j.resmic.2016.05.008openalex-snapshot
Phenotype MicroArray™ system in the study of fungal functional diversity and catabolic versatility
inferredcites →https://doi.org/10.1016/j.ympev.2005.07.006openalex-snapshot
Phylogenetic relationships between members of the crucifer pathogenic Leptosphaeria maculans species complex as shown by mating type (MAT1-2), actin, and β-tubulin sequences
inferredcites →https://doi.org/10.1016/s0953-7562(09)80497-8openalex-snapshot
Intraspecific variation in soluble mycelial protein and esterase patterns of Leptosphaeria maculans French isolates
inferredcites →https://doi.org/10.1017/s0953756203008554openalex-snapshot
Molecular phylogeny of the Leptosphaeria maculans-L. biglobosa species complex
inferredcites →https://doi.org/10.1023/a:1025597622490openalex-snapshot
Screening and identification of resistance to Leptosphaeria maculans (stem canker) in Brassica napus accessions
inferredcites →https://doi.org/10.1023/a:1026189225466openalex-snapshot
A 10-year Survey of Populations of Leptosphaeria maculans in France Indicates a Rapid Adaptation Towards the Rlm1 Resistance Gene of Oilseed Rape
inferredcites →https://doi.org/10.1046/j.1365-3059.1999.00333.xopenalex-snapshot
Differentiating A and B groups of Leptosphaeria maculans , causal agent of stem canker (blackleg) of oilseed rape
inferredcites →https://doi.org/10.1046/j.1365-3059.2000.00503.xopenalex-snapshot
Leptosphaeria maculans causing stem canker of oilseed rape in China
inferredcites →https://doi.org/10.1046/j.1365-3059.2001.00546.xopenalex-snapshot
Epidemiology and management of Leptosphaeria maculans (phoma stem canker) on oilseed rape in Australia, Canada and Europe
inferredcites →https://doi.org/10.1046/j.1365-3059.2002.00689.xopenalex-snapshot
Colonization of winter oilseed rape tissues by A/Tox + and B/Tox 0 Leptosphaeria maculans (phoma stem canker) in France and England
inferredcites →https://doi.org/10.1071/bt9940001openalex-snapshot
Non-aggressive Strains of the Blackleg Fungus, Leptosphaeria maculans , Are Present in Australia and Can Be Distinguished From Aggressive Strains by Molecular Analysis
inferredcites →https://doi.org/10.1071/cp16401openalex-snapshot
Insights into fighting against blackleg disease of Brassica napus in Canada
inferredcites →https://doi.org/10.1071/cp16404openalex-snapshot
Changes in farming practices impact on spore release patterns of the blackleg pathogen, Leptosphaeria maculans
inferredcites →https://doi.org/10.1071/ea9760911openalex-snapshot
The role of pycnidiospores of Leptosphaeria maculans in the spread of blackleg disease in rape
inferredcites →https://doi.org/10.1078/0944-5013-00099openalex-snapshot
Strain typing of Polish Leptosphaeria maculans isolates supports at the genomic level the multi-species concept of aggressive and non-aggressive strains
inferredcites →https://doi.org/10.1080/00173134.2011.649016openalex-snapshot
Influence of meteorological parameters onLeptosphaeria maculansandL. biglobosaspore release in central and eastern Poland
inferredcites →https://doi.org/10.1080/01621459.1963.10500845openalex-snapshot
Hierarchical Grouping to Optimize an Objective Function
inferredcites →https://doi.org/10.1080/07060661003594109openalex-snapshot
Frequency of avirulence genes inLeptosphaeria maculansin western Canada
inferredcites →https://doi.org/10.1080/07060669209500904openalex-snapshot
History, occurrence, impact, and control of blackleg of rapeseed
inferredcites →https://doi.org/10.1080/07060669209500907openalex-snapshot
The blackleg fungus: phytotoxins and phytoalexins
inferredcites →https://doi.org/10.1080/07060669509500712openalex-snapshot
Glucose phosphate isomerase polymorphisms distinguish weakly virulent from highly virulent strains ofLeptosphaeria maculans
inferredcites →https://doi.org/10.1080/11263504.2017.1284166openalex-snapshot
A simple method for measuring fungal metabolic quotient and comparing carbon use efficiency of different isolates: Application to Mediterranean leaf litter fungi
inferredcites →https://doi.org/10.1094/pd-89-0097openalex-snapshot
Seasonal and Diurnal Patterns of Spore Dispersal by Leptosphaeria maculans from Canola Stubble in Relation to Environmental Conditions
inferredcites →https://doi.org/10.1094/pdis-12-20-2735-pdnopenalex-snapshot
First Report of Leptosphaeria biglobosa ‘canadensis’ Causing Blackleg on Oilseed Rape (Brassica napus) in China
inferredcites →https://doi.org/10.1094/pdis.2003.87.6.752aopenalex-snapshot
Breakdown of a Brassica rapa subsp. sylvestris Single Dominant Blackleg Resistance Gene in B. napus Rapeseed by Leptosphaeria maculans Field Isolates in Australia
inferredcites →https://doi.org/10.1094/phyto-95-1061openalex-snapshot
Analysis of Leptosphaeria maculans Race Structure in a Worldwide Collection of Isolates
inferredcites →https://doi.org/10.1094/phyto-98-3-0321openalex-snapshot
Occurrence of a New Subclade of Leptosphaeria biglobosa in Western Australia
inferredcites →https://doi.org/10.1111/j.1365-3059.2003.00930.xopenalex-snapshot
Effects of temperature on maturation of pseudothecia of Leptosphaeria maculans and L. biglobosa on oilseed rape stem debris
inferredcites →https://doi.org/10.1111/j.1365-3059.2006.01354.xopenalex-snapshot
Resistance to Leptosphaeria maculans (phoma stem canker) in Brassica napus (oilseed rape) induced by L. biglobosa and chemical defence activators in field and controlled environments
inferredcites →https://doi.org/10.1111/j.1365-3059.2008.02014.xopenalex-snapshot
Systemic growth of Leptosphaeria maculans from cotyledons to hypocotyls in oilseed rape: influence of number of infection sites, competitive growth and host polygenic resistance
inferredcites →https://doi.org/10.1111/j.1365-3059.2009.02149.xopenalex-snapshot
The Leptosphaeria maculans – Leptosphaeria biglobosa species complex in the American continent
inferredcites →https://doi.org/10.1111/j.1439-0434.1989.tb04894.xopenalex-snapshot
Differences Between Aggressive and Non‐Aggressive Single Spore Lines of Leptosphaeria maculans in Cultural Characteristics and Phytotoxin Production
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03049.xopenalex-snapshot
Quantitative resistance increases the durability of qualitative resistance to Leptosphaeria maculans in Brassica napus
inferredcites →https://doi.org/10.1111/nph.14411openalex-snapshot
Life, death and rebirth of avirulence effectors in a fungal pathogen of B rassica crops, L eptosphaeria maculans
inferredcites →https://doi.org/10.1111/ppa.12146openalex-snapshot
Leptosphaeria spp., phoma stem canker and potential spread of L . maculans on oilseed rape crops in C hina
inferredcites →https://doi.org/10.1111/ppa.12489openalex-snapshot
Race structure and frequency of avirulence genes in the western Canadian Leptosphaeria maculans pathogen population, the causal agent of blackleg in brassica species
inferredcites →https://doi.org/10.1111/ppa.12589openalex-snapshot
Phoma leaf spot of wasabi ( Wasabia japonica ) caused by Leptosphaeria biglobosa
inferredcites →https://doi.org/10.1111/ppa.13453openalex-snapshot
Effects of cultivar resistance and fungicide application on stem canker of oilseed rape ( Brassica napus ) and potential interseasonal transmission of Leptosphaeria spp. inoculum
inferredcites →https://doi.org/10.1139/w06-133openalex-snapshot
The phytopathogenic fungi Leptosphaeria maculans and Leptosphaeria biglobosa: chemotaxonomical characterization of isolates and metabolite production in different culture media
inferredcites →https://doi.org/10.1146/annurev.phyto.44.070505.143417openalex-snapshot
Coexistence of Related Pathogen Species on Arable Crops in Space and Time
inferredcites →https://doi.org/10.1186/s12864-020-06893-4openalex-snapshot
Identification of resistance loci in Chinese and Canadian canola/rapeseed varieties against Leptosphaeria maculans based on genome-wide association studies
inferredcites →https://doi.org/10.1371/journal.pone.0211744openalex-snapshot
The wood decay fungus Cerrena unicolor adjusts its metabolism to grow on various types of wood and light conditions
inferredcites →https://doi.org/10.1631/jzus.b1000007openalex-snapshot
Global nutrient profiling by Phenotype MicroArrays: a tool complementing genomic and proteomic studies in conidial fungi
inferredcites →https://doi.org/10.3114/sim0004openalex-snapshot
Redisposition of phoma-like anamorphs in Pleosporales
inferredcites →https://doi.org/10.3389/fmicb.2018.00115openalex-snapshot
Metabolic and Genetic Properties of Petriella setifera Precultured on Waste
inferredcites →https://doi.org/10.3389/fpls.2016.01513openalex-snapshot
Genome-wide Association Study Identifies New Loci for Resistance to Leptosphaeria maculans in Canola
inferredcites →https://doi.org/10.3389/fpls.2018.01622openalex-snapshot
Stable Quantitative Resistance Loci to Blackleg Disease in Canola (Brassica napus L.) Over Continents
inferredcites →https://doi.org/10.3390/agronomy11061171openalex-snapshot
Warm and Wet Autumns Favour Yield Losses of Oilseed Rape Caused by Phoma Stem Canker
inferredcites →https://doi.org/10.3390/ijms20071668openalex-snapshot
A New Subclade of Leptosphaeria biglobosa Identified from Brassica rapa
inferredcites →https://doi.org/10.3390/ijms21124235openalex-snapshot
How Do Trichoderma Genus Fungi Win a Nutritional Competition Battle against Soft Fruit Pathogens? A Report on Niche Overlap Nutritional Potentiates
inferredcites →https://doi.org/10.5586/aa.2011.012openalex-snapshot
Characterization of two coexisting pathogen populations of Leptosphaeria spp., the cause of stem canker of brassicas
inferredcites →https://doi.org/10.5586/aa.2013.055openalex-snapshot
Loop-mediated isothermal amplification as a good tool to study changing Leptosphaeria populations in oilseed rape plants and air samples
inferredcites →https://doi.org/10.5937/ratpov53-8997openalex-snapshot
The first occurrence of stem canker on oilseed rape caused by Leptosphaeria biglobosa in Serbia
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4781016openalex-extracted
Slipping Through the Cracks: Challenges and Prospects for Managing Fungal Pathogens Involved in Plant Disease Complexes
inferred← citeshttps://doi.org/10.1002/ps.70643openalex-snapshot
Temporal dynamics of co‐inoculation of Leptosphaeria maculans and Leptosphaeria biglobosa determine interspecific competition and disease development on oilseed rape
inferred← citeshttps://doi.org/10.1002/ps.71014openalex-snapshot
Disease control in oilseed rape: Current insights and perspectives for next‐generation integrated pest management
inferred← citeshttps://doi.org/10.1002/ps.7799openalex-snapshot
Co‐inoculation timing affects the interspecific interactions between phoma stem canker pathogens Leptosphaeria maculans and Leptosphaeria biglobosa
inferred← citeshttps://doi.org/10.1007/s11356-025-37377-1openalex-snapshot
Diversity of dark septate endophytes (DSEs) around Kalina Pound (Poland) and their potential to improve stress tolerance in Lolium perenne L. exposed to polycyclic aromatic hydrocarbons (PAHs)
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Functional Microbial Diversity in the Study of Soils of Various Ecosystems
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inferred← citeshttps://doi.org/10.1016/j.apsoil.2026.107024openalex-snapshot
Response of soil nutrient pools and microbiomes to recurrent wildfire disturbance and varying burn severities in a mixed conifer forest
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/10.1111/ppa.70261openalex-snapshot
Soil Pathobiome in Agroecosystems and Forests
inferred← citeshttps://doi.org/10.1186/s12915-023-01726-8openalex-snapshot
Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.31545/intagr/170884openalex-snapshot
Selection of redox dye and inoculum conditions for the optimisation of respirometric indices in Verticillium and Trichoderma
inferred← citeshttps://doi.org/10.31545/intagr/217847openalex-snapshot
Soil microbiome as an essential player in climate change and plant health control: a review
inferred← citeshttps://doi.org/10.3390/applmicrobiol5040114openalex-snapshot
Identification of Filamentous Fungi Present in Prolonged Fermentations of Coffea arabica L. var. Castillo
inferred← citeshttps://doi.org/10.3390/metabo13060759openalex-snapshot
Differences in the Production of Extracellular Polymeric Substances (EPS) and Other Metabolites of Plenodomus (Leptosphaeria) Infecting Winter Oilseed Rape (Brassica napus L.)
inferred← citeshttps://doi.org/10.3390/microorganisms11010224openalex-snapshot
Microbial-Based Products to Control Soil-Borne Pathogens: Methods to Improve Efficacy and to Assess Impacts on Microbiome
inferred← citeshttps://doi.org/10.6084/m9.figshare.24522654openalex-snapshot
Additional file 1 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.24522873openalex-snapshot
Additional file 2 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636946openalex-snapshot
Additional file 3 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636949openalex-snapshot
Additional file 4 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636952openalex-snapshot
Additional file 5 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636955openalex-snapshot
Additional file 6 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636958openalex-snapshot
Additional file 7 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636961openalex-snapshot
Additional file 8 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636964openalex-snapshot
Additional file 9 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636967openalex-snapshot
Additional file 10 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636970openalex-snapshot
Additional file 11 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636976openalex-snapshot
Additional file 12 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636979openalex-snapshot
Additional file 13 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636982openalex-snapshot
Additional file 14 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636988openalex-snapshot
Additional file 15 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636991openalex-snapshot
Additional file 16 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26636997openalex-snapshot
Additional file 17 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637000openalex-snapshot
Additional file 18 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637003openalex-snapshot
Additional file 19 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637006openalex-snapshot
Additional file 20 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637009openalex-snapshot
Additional file 21 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637012openalex-snapshot
Additional file 22 of Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
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