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New specific quantitative real‐time PCR assays shed light on the epidemiology of two species of the Leptosphaeria maculans – Leptosphaeria biglobosa species complex
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Outgoing claims: the papers this work cites, builds on, or argues with.
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/s00248-019-01340-8openalex-snapshot
Crop Residues in Wheat-Oilseed Rape Rotation System: a Pivotal, Shifting Platform for Microbial Meetings
inferredcites →https://doi.org/10.1007/s10453-011-9228-9openalex-snapshot
Quantitative PCR analysis of abundance of airborne propagules of Leptosphaeria species in air samples from different regions of Poland
inferredcites →https://doi.org/10.1007/s10658-004-4421-0openalex-snapshot
Patterns of ascospore release in relation to phoma stem canker epidemiology in England (Leptosphaeria maculans) and Poland (Leptosphaeria biglobosa)
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/s10658-014-0513-7openalex-snapshot
Phoma stem canker disease on oilseed rape (Brassica napus) in China is caused by Leptosphaeria biglobosa ‘brassicae’
inferredcites →https://doi.org/10.1016/j.femsle.2005.09.041openalex-snapshot
Agrobacterium tumefaciens-mediated transformation of Leptosphaeria spp. and Oculimacula spp. with the reef coral gene DsRed and the jellyfish gene gfp
inferredcites →https://doi.org/10.1016/j.tifs.2014.03.008openalex-snapshot
Guidelines for validation of qualitative real-time PCR methods
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/b:ejpp.0000015359.61910.3bopenalex-snapshot
Methods for Sampling and Assessment in Relation to the Spatial Pattern of Phoma Stem Canker (Leptosphaeria maculans) in Oilseed Rape
inferredcites →https://doi.org/10.1046/j.1365-3059.2001.00526.xopenalex-snapshot
Development of phoma lesions on oilseed rape leaves inoculated with ascospores of A‐group or B‐group Leptosphaeria maculans (stem canker) at different temperatures and wetness durations
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/10.1046/j.1365-3059.2002.00726.xopenalex-snapshot
Effects of timing of Leptosphaeria maculans ascospore release and fungicide regime on phoma leaf spot and phoma stem canker development on winter oilseed rape ( Brassica napus ) in southern England
inferredcites →https://doi.org/10.1051/ocl.2002.0079openalex-snapshot
DEFENSE DES CULTURES La nécrose du collet du colza : analyse de la distribution du champignon dans la plante à l’aide d’outils moléculaires
inferredcites →https://doi.org/10.1071/cp16308openalex-snapshot
Analysis of Leptosphaeria species complex causing phoma leaf spot and stem canker of winter oilseed rape (Brassica napus) in the Czech Republic
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.1365-3059.1994.tb02685.xopenalex-snapshot
Variation in host range, systemic infection and epidemiology of Leptosphaeria maculans
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.1365-3059.2008.01841.xopenalex-snapshot
Strategies to prevent spread of Leptosphaeria maculans (phoma stem canker) onto oilseed rape crops in China; costs and benefits
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.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/mpp.12994openalex-snapshot
Impact of a resistance gene against a fungal pathogen on the plant host residue microbiome: The case of the Leptosphaeria maculans–Brassica napus pathosystem
inferredcites →https://doi.org/10.1111/nph.12178openalex-snapshot
The dispensable chromosome of L eptosphaeria maculans shelters an effector gene conferring avirulence towards B rassica rapa
inferredcites →https://doi.org/10.1128/aem.72.1.185-191.2006openalex-snapshot
Genetic Variability and Distribution of Mating Type Alleles in Field Populations of Leptosphaeria maculans from France
inferredcites →https://doi.org/10.1139/b01-019openalex-snapshot
The teleomorph of the weakly aggressive segregate ofLeptosphaeriamaculans
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/10.1186/1471-2164-15-891openalex-snapshot
Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens
inferredcites →https://doi.org/10.1371/journal.pone.0084924openalex-snapshot
Assessing Quantitative Resistance against Leptosphaeria maculans (Phoma Stem Canker) in Brassica napus (Oilseed Rape) in Young Plants
inferredcites →https://doi.org/10.1371/journal.pone.0207988openalex-snapshot
Metabarcoding targeting the EF1 alpha region to assess Fusarium diversity on cereals
inferredcites →https://doi.org/10.1373/clinchem.2008.112797openalex-snapshot
The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments
inferredcites →https://doi.org/10.3389/fpls.2017.00119openalex-snapshot
Using Population and Comparative Genomics to Understand the Genetic Basis of Effector-Driven Fungal Pathogen Evolution
inferredcites →https://doi.org/10.3390/ijms20071668openalex-snapshot
A New Subclade of Leptosphaeria biglobosa Identified from Brassica rapa
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.71339openalex-snapshot
Discovery and characterisation of succinate dehydrogenase inhibitor resistance in Plenodomus biglobosus (phoma stem canker of oilseed rape)
inferred← citeshttps://doi.org/10.1002/ps.7248openalex-snapshot
Effective control of Leptosphaeria maculans increases importance of L. biglobosa as a cause of phoma stem canker epidemics on oilseed rape
inferred← citeshttps://doi.org/10.1002/ps.7275openalex-snapshot
Leptosphaeria biglobosa inhibits the production of sirodesmin PL by L. maculans
inferred← citeshttps://doi.org/10.1002/ps.7800openalex-snapshot
Efficient qPCR estimation and discrimination of airborne inoculum of Leptosphaeria maculans and L. biglobosa , the causal organisms of phoma leaf spotting and stem canker of oilseed rape
inferred← citeshttps://doi.org/10.1007/s00122-024-04641-wopenalex-snapshot
Breeding and management of major resistance genes to stem canker/blackleg in Brassica crops
inferred← citeshttps://doi.org/10.1007/s11274-026-05168-6openalex-snapshot
Antagonism-driven upregulation of the pulcherriminic acid biosynthetic pathway in Metschnikowia pulcherrima and Leptosphaeria maculans interaction
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/10.1079/planthealthcases.2024.0007openalex-snapshot
Phoma Stem Canker (Blackleg) of Oilseed Rape (Canola) and Other Brassica Crops
inferred← citeshttps://doi.org/10.1080/07060661.2022.2031300openalex-snapshot
Differential growth of Leptosphaeria maculans in the stem of susceptible and partially resistant oilseed rape (Brassica napus L.) genotypes
inferred← citeshttps://doi.org/10.1094/pbiomes-07-23-0069-ropenalex-snapshot
A Specific Resistance Gene to Leptosphaeria maculans, Rlm11, Has a Limited Impact on Brassica napus Mycobiota Compared with Plant Compartment or Cropping Season Effects
inferred← citeshttps://doi.org/10.1094/pdis-10-22-2308-reopenalex-snapshot
Development of a Duplex qPCR System for Detection and Quantification of the Two Canola Blackleg Pathogens Leptosphaeria biglobosa and L. maculans
inferred← citeshttps://doi.org/10.1111/1758-2229.70034openalex-snapshot
To be or not to be a nonhost species: A case study of the Leptosphaeria maculans and Brassica carinata interaction
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/ppa.13801openalex-snapshot
A new set of international Leptosphaeria maculans isolates as a resource for elucidation of the basis and evolution of blackleg disease on Brassica napus
inferred← citeshttps://doi.org/10.1111/ppa.14018openalex-snapshot
Strategic genetic insights and integrated approaches for successful management of blackleg in canola/rapeseed farming
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/10.21203/rs.3.rs-10056100/v1openalex-snapshot
Blackleg in Swedish winter oilseed rape, causal pathogens, and race identification of Plenodomus lingam
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/plants11070996openalex-snapshot
Less Virulent Leptosphaeria biglobosa Immunizes the Canola Plant to Resist Highly Virulent L. maculans, the Blackleg Pathogen
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
inferred← citeshttps://doi.org/10.70675/91fb6ca0z04acz43f2z9d8dz647e79e1a74dopenalex-snapshot
Incidence des résistances Rlm11 et RlmS du colza sur le microbiote fongique associé à Leptosphaeria maculans et sur la sélection des allèles d'avirulence au cours du cycle infectieux
inferred← citeshttps://doi.org/10.70675/ae23be89z6d9ez4a77zb907z30aaa63b60a4openalex-snapshot
Dissection transcriptomique de la biologie de Leptosphaeria maculans lors de ses interactions avec son hôte (le colza) et avec un membre du complexe d'espèces, Leptosphaeria biglobosa
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