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Phylogenetic Analysis of Cercospora and Mycosphaerella Based on the Internal Transcribed Spacer Region of Ribosomal DNA

https://doi.org/10.1094/phyto.2001.91.7.648
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/fgbi.1997.0961openalex-snapshot
Efficient Cloning of Ascomycete Mating Type Genes by PCR Amplification of the ConservedMATHMG Box
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1016/0048-4059(78)90029-2openalex-snapshot
Cercosporin, a phytotoxin from Cercospora spp
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/s0031-9422(00)86794-1openalex-snapshot
Screening of the genus Cercospora for secondary metabolites☆
inferredcites →https://doi.org/10.1017/s0953756299008680openalex-snapshot
Phylogenetic relationships among some cercosporoid anamorphs of Mycosphaerella based on rDNA sequence analysis
inferredcites →https://doi.org/10.1080/00275514.1996.12026671openalex-snapshot
Species of Mycosphaerella and Their Anamorphs Associated with Leaf Blotch Disease of Eucalyptus in South Africa
inferredcites →https://doi.org/10.1080/00275514.1996.12026714openalex-snapshot
Morphological and molecular studies on Auriculariopsis albomellea and Phlebia albida and a reassessment of A. ampla
inferredcites →https://doi.org/10.1080/00275514.2001.12063227openalex-snapshot
Phylogenetic analyses of the ITS region of ribosomal DNA reveal that Septoria passerinii from barley is closely related to the wheat pathogen Mycosphaerella graminicola
inferredcites →https://doi.org/10.1093/aibsbulletin/4.3.11-dopenalex-snapshot
A Monograph of the Fungus Genus Cercospora
inferredcites →https://doi.org/10.1093/nar/25.17.3389openalex-snapshot
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040454openalex-snapshot
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
inferredcites →https://doi.org/10.1094/pd-67-842openalex-snapshot
Gray Leaf Spot of Corn: A Disease on the Move
inferredcites →https://doi.org/10.1094/phyto-61-1477openalex-snapshot
Triglycerides and Cercosporin from Cercospora beticola: Fungal Growth and Cercosporin Production
inferredcites →https://doi.org/10.1094/phyto-79-213openalex-snapshot
Regulation of Cercosporin Accumulation in Culture by Medium and Temperature Manipulation
inferredcites →https://doi.org/10.1094/phyto.1998.88.12.1269openalex-snapshot
Sibling Species of Cercospora Associated with Gray Leaf Spot of Maize
inferredcites →https://doi.org/10.1094/phyto.2000.90.5.486openalex-snapshot
Genetic Relatedness of African and United States Populations of Cercospora zeae-maydis
inferredcites →https://doi.org/10.1128/aem.56.10.3052-3056.1990openalex-snapshot
Genetic Transformation of the Biocontrol Fungus Gliocladium virens to Benomyl Resistance
inferredcites →https://doi.org/10.1128/aem.57.10.2940-2945.1991openalex-snapshot
Mutants of Cercospora kikuchii Altered in Cercosporin Synthesis and Pathogenicity
inferredcites →https://doi.org/10.1128/jcm.37.6.2031-2033.1999openalex-snapshot
Lacazia loboi gen. nov., comb. nov., the Etiologic Agent of Lobomycosis
inferredcites →https://doi.org/10.2307/3760971openalex-snapshot
Morphological and Molecular Studies on Auriculariopsis albomellea and Phlebia albida and a Reassessment of A. ampla
inferredcites →https://doi.org/10.2307/3761362openalex-snapshot
Mycosphaerella spp. and Their Anamorphs Associated with Leaf Spot Diseases of Eucalyptus
inferredcites →https://doi.org/10.2307/3761758openalex-snapshot
Phylogenetic Analyses of the ITS Region of Ribosomal DNA Reveal That Septoria passerinii from Barley Is Closely Related to the Wheat Pathogen Mycosphaerella graminicola
inferredcites →https://doi.org/10.5962/p.415198openalex-snapshot
Planistromellaceae, a new family in the Dothideales

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Is morphology in Cercospora a reliable reflection of generic affinity?
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Novel endophytic fungi from Pinus: introducing three new genera and six new species within Capnodiales (Ascomycota, Dothideomycetes) sensu lato
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Cercosporin
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Fungal and Bacterial Diseases
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Dothideomycetes
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Isolation and Characterization of the Mating-Type Idiomorphs from the Wheat Septoria Leaf Blotch Fungus Mycosphaerella graminicola
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The Genomes of Mycosphaerella graminicola and M. fijiensis
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Engineering Resistance to Sigatoka
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Analysis of genotypic diversity inCercospora beticola Sacc. field isolates
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Quantitative trait locus analysis of gray leaf spot resistance in the maize IBM Syn10 DH population
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Advancing fungal phylogenetics: integrating modern sequencing, dark taxa discovery, and machine learning
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Sequence diversity of mating-type genes in Phaeosphaeria avenaria
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Cloning and analysis of the mating-type idiomorphs from the barley pathogen Septoria passerinii
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Quantitative phenotyping of grey leaf spot disease in maize using real-time PCR
inferred← citeshttps://doi.org/10.1007/s10658-023-02790-0openalex-snapshot
Unraveling the prevalence of soil-borne fungal pathogens in the North China Plain: a global analysis approach
inferred← citeshttps://doi.org/10.1007/s11046-009-9194-8openalex-snapshot
Pseudocercospora griseola Causing Angular Leaf Spot on Phaseolus vulgaris Produces 1,8-Dihydroxynaphthalene-Melanin
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Infection of Barley by Ramularia collo-cygni: Scanning Electron Microscopic Investigations
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Genetic Diversity of Cercospora kikuchii Isolates From Soybean Cultured in Argentina as Revealed by Molecular Markers and Cercosporin Production
inferred← citeshttps://doi.org/10.1007/s11557-006-0101-0openalex-snapshot
A phylogenetic study of some Septoria species pathogenic to Asteraceae based on ITS ribosomal DNA sequences
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Cercospora species associated with soybean diseases in Russia
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Genetic variation of Phoma sorghina isolates from Southern Africa and Texas
inferred← citeshttps://doi.org/10.1007/s13225-010-0033-5openalex-snapshot
New Teratosphaeria species occurring on eucalypts in Australia
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The evolution of species concepts and species recognition criteria in plant pathogenic fungi
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Naming and outline of Dothideomycetes–2014 including proposals for the protection or suppression of generic names
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Species concepts of Dothideomycetes: classification, phylogenetic inconsistencies and taxonomic standardization
inferred← citeshttps://doi.org/10.1007/s40858-015-0053-5openalex-snapshot
Cercospora zeina is the main species causing gray leaf spot in southern and central Brazilian maize regions
inferred← citeshttps://doi.org/10.1007/s40858-017-0205-xopenalex-snapshot
Multi-host species of Cercospora are associated with Cercospora leaf blight and purple seed stain of soybean
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Understanding the genetics of Cercospora leaf spot (CLS) resistance in mung bean (Vigna radiata L. Wilczek)
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Frogeye leaf spot caused by Cercospora sojina: A review
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Identification of Cercospora species associated with Cercospora Leaf Blight of soybean in Brazil
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Six lineages of Cercospora are responsible for Cercospora leaf blight and purple seed stain on soybean in Brazil
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Population genetic structure of Cercospora cf. flagellaris, the dominant causal agent of bean Cercospora leaf spot disease using ISSR markers
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Baseline sensitivity of Cercospora zeae-maydis to pydiflumetofen, a new succinate dehydrogenase inhibitor fungicide
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Mating type gene analysis in apparently asexual Cercospora species is suggestive of cryptic sex
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Identification and genetic mapping of highly polymorphic microsatellite loci from an EST database of the septoria tritici blotch pathogen Mycosphaerella graminicola
inferred← citeshttps://doi.org/10.1016/j.fgb.2006.11.004openalex-snapshot
Mating-type genes and the genetic structure of a world-wide collection of the tomato pathogen Cladosporium fulvum
inferred← citeshttps://doi.org/10.1016/j.fgb.2006.12.005openalex-snapshot
Discovery of a functional Mycosphaerella teleomorph in the presumed asexual barley pathogen Septoria passerinii
inferred← citeshttps://doi.org/10.1016/j.fgb.2007.12.005openalex-snapshot
Intraspecific comparison and annotation of two complete mitochondrial genome sequences from the plant pathogenic fungus Mycosphaerella graminicola
inferred← citeshttps://doi.org/10.1016/j.fgb.2013.10.011openalex-snapshot
The heterothallic sugarbeet pathogen Cercospora beticola contains exon fragments of both MAT genes that are homogenized by concerted evolution
inferred← citeshttps://doi.org/10.1016/j.fgb.2021.103527openalex-snapshot
Population genetic structure and migration patterns of the maize pathogenic fungus, Cercospora zeina in East and Southern Africa
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Evaluation of the potential for sexual reproduction in field populations of Cercospora beticola from USA
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Cryptic diversity, pathogenicity, and evolutionary species boundaries in Cercospora populations associated with Cercospora leaf spot of Beta vulgaris
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Fungal endophyte diversity and community patterns in healthy and yellowing leaves of Citrus limon
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A comparative genome analysis of Cercospora sojina with other members of the pathogen genus Mycosphaerella on different plant hosts
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Anatase as an alternative application for preventing biodeterioration of mortars: Evaluation and comparison with other biocides
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Didymella pisi sp. nov., the teleomorph of Ascochyta pisi
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Molecular characterization of the phytopathogen C. theae (Petch) – Causative of birds eye spot infection in Camellia sinensis host through DNA polymorphism and proteome analysis
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Attributes and congruence of three molecular data sets: Inferring phylogenies among Septoria-related species from woody perennial plants
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Cloning and characterization of the mating type (MAT) locus from Ascochyta rabiei (teleomorph: Didymella rabiei) and a MAT phylogeny of legume-associated Ascochyta spp.
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Identity and conservation of mating type genes in geographically diverse isolates of Phaeosphaeria nodorum
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Genetics and Genomics of Mycosphaerella graminicola: A Model for the Dothideales
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The barley scald pathogen Rhynchosporium secalis is closely related to the discomycetes Tapesia and Pyrenopeziza
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Host-parasite relationships among bolete infecting Hypomyces species
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Mycosphaerella punctiformis revisited: morphology, phylogeny, and epitypification of the type species of the genus Mycosphaerella (Dothideales, Ascomycota)
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Eyespot of Cereals Revisited: ITS phylogeny Reveals New Species Relationships
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Identification of QTL for Target Leaf Spot resistance in Sorghum bicolor and investigation of relationships between disease resistance and variation in the MAMP response
inferred← citeshttps://doi.org/10.1051/limn/09004openalex-snapshot
A heterotrophic nanoflagellate grazing on the toxic CyanobacteriumMicrocystis aeruginosa
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Identification of Mycosphaerella species associated with Eucalyptus nitens leaf defoliation in South Africa
inferred← citeshttps://doi.org/10.1079/cabicompendium.49057openalex-snapshot
Mycosphaerella dearnessii (brown spot needle blight)
inferred← citeshttps://doi.org/10.1079/cabicompendium.49059openalex-snapshot
Mycosphaerella pini (Dothistroma blight)
inferred← citeshttps://doi.org/10.1080/00275514.2024.2383114openalex-snapshot
Phylogenetic analyses show the Select Agent Coniothyrium glycines represents a single species that has significant morphological and genetic variation
inferred← citeshttps://doi.org/10.1080/03235408.2021.1895478openalex-snapshot
Morphological and genetic diversity of Cercospora beticola Sacc isolates in Morocco
inferred← citeshttps://doi.org/10.1080/03235408.2021.2000782openalex-snapshot
Identification and molecular characterisation of cercospora leaf spot disease pathogen on cowpea (Vigna unguiculataL. Walp)
inferred← citeshttps://doi.org/10.1080/03235408.2023.2216356openalex-snapshot
Overview of sugar beet leaf spot disease caused by Cercospora beticola Sacc
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An improved PCR assay for species-specific detection and quantification of Cercospora beticola
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Recent advances related to poplar leaf spot and canker caused by Septoria musiva
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Establishment and Application of PCR-SSCP Profile for Molecular Typing ofCordycepsFungi
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Phylogenetic analyses ofSeptoriaspecies based on the ITS and LSU-D2 regions of nuclear ribosomal DNA
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Cercosporella acroptili and Cercosporella centaureicola sp. nov.—potential biological control agents of Russian knapweed and yellow starthistle, respectively
inferred← citeshttps://doi.org/10.1080/15572536.2006.11832811openalex-snapshot
Malazy, a degenerate, species-specific transposable element in Cercospora zeae-maydis
inferred← citeshttps://doi.org/10.1080/15572536.2007.11832584openalex-snapshot
The systematic position of Phaeocryptopus gaeumannii
inferred← citeshttps://doi.org/10.1093/dnares/dsx035openalex-snapshot
Genome sequencing and comparative genomics reveal the potential pathogenic mechanism of Cercospora sojina Hara on soybean
inferred← citeshttps://doi.org/10.1093/molbev/msl169openalex-snapshot
Origin and Domestication of the Fungal Wheat Pathogen Mycosphaerella graminicola via Sympatric Speciation
inferred← citeshttps://doi.org/10.1093/treephys/tpae003openalex-snapshot
Physiological, metabolic and hormonal responses of two Pinus spp. with contrasting susceptibility to brown-spot needle blight disease
inferred← citeshttps://doi.org/10.1094/mpmi-03-17-0054-ropenalex-snapshot
Complementation of CTB7 in the Maize Pathogen Cercospora zeina Overcomes the Lack of In Vitro Cercosporin Production
inferred← citeshttps://doi.org/10.1094/mpmi-03-25-0031-ropenalex-snapshot
A Population Genomics Approach to Understand the Diversity, Migration, and Reproduction of the Rice Pathogen Cercospora janseana
inferred← citeshttps://doi.org/10.1094/mpmi-06-22-0138-ropenalex-snapshot
Pathogenicity Variation in Two Genomes of Cercospora Species Causing Gray Leaf Spot in Maize
inferred← citeshttps://doi.org/10.1094/pdis-03-23-0588-reopenalex-snapshot
Characterization of QoI-Fungicide Resistance in Cercospora Isolates Associated with Cercospora Leaf Blight of Soybean from the Southern United States
inferred← citeshttps://doi.org/10.1094/pdis-05-12-0472-pdnopenalex-snapshot
First Report of Passalora Leaf Spot of Quinoa Caused by Passalora dubia in the United States
inferred← citeshttps://doi.org/10.1094/phyto-02-16-0084-fiopenalex-snapshot
Cercospora zeinafrom Maize in South Africa Exhibits High Genetic Diversity and Lack of Regional Population Differentiation
inferred← citeshttps://doi.org/10.1094/phyto-07-13-0200-ropenalex-snapshot
Development of a Quantitative Polymerase Chain Reaction Detection Protocol for Cercospora kikuchii in Soybean Leaves and Its Use for Documenting Latent Infection as Affected by Fungicide Applications
inferred← citeshttps://doi.org/10.1094/phyto-09-12-0229-ropenalex-snapshot
Mating-Type Distribution and Genetic Diversity of Cercospora sojina Populations on Soybean from Arkansas: Evidence for Potential Sexual Reproduction
inferred← citeshttps://doi.org/10.1094/phyto-09-22-0348-ropenalex-snapshot
Virulence Associations and Global Context of AvrStb6 Genetic Diversity in Iranian Populations of Zymoseptoria tritici
inferred← citeshttps://doi.org/10.1094/phyto-09-23-0315-kcopenalex-snapshot
Remarkably High Internal Transcribed Spacer Haplotype Diversity of the Fungal Select Agent Coniothyrium glycines Discovered Throughout Its Range in Sub-Saharan Africa
inferred← citeshttps://doi.org/10.1094/phyto-12-15-0332-ropenalex-snapshot
Cercospora cf. flagellaris and Cercospora cf. sigesbeckiae Are Associated with Cercospora Leaf Blight and Purple Seed Stain on Soybean in North America
inferred← citeshttps://doi.org/10.1094/phyto-12-16-0448-ropenalex-snapshot
Description of the Nicotiana benthamiana−Cercospora nicotianae Pathosystem
inferred← citeshttps://doi.org/10.1094/phyto-12-19-0446-ropenalex-snapshot
Field Characterization of Partial Resistance to Gray Leaf Spot in Elite Maize Germplasm
inferred← citeshttps://doi.org/10.1094/phyto-95-0257openalex-snapshot
Vegetative Compatibility Groups in Cercospora kikuchii, the Causal Agent of Cercospora Leaf Blight and Purple Seed Stain in Soybean
inferred← citeshttps://doi.org/10.1094/phyto-95-0951openalex-snapshot
Distinct Species Exist Within theCercospora apiiMorphotype
inferred← citeshttps://doi.org/10.1094/phyto-97-2-0132openalex-snapshot
Development of Nested Polymerase Chain Reaction Detection ofMycosphaerellaspp. and Its Application to the Study of Leaf Disease inEucalyptusPlantations
inferred← citeshttps://doi.org/10.1094/phyto-97-6-0737openalex-snapshot
Detection ofEutypa lataandEutypella vitisin Grapevine by Nested Multiplex Polymerase Chain Reaction
inferred← citeshttps://doi.org/10.1094/phyto-97-7-0825openalex-snapshot
Characterization and Distribution of Mating Type Genes in the Dothistroma Needle Blight Pathogens
inferred← citeshttps://doi.org/10.1094/phyto.2001.91.12.1181openalex-snapshot
DNA Fingerprint Probe from Mycosphaerella graminicola Identifies an Active Transposable Element
inferred← citeshttps://doi.org/10.1094/phyto.2002.92.4.439openalex-snapshot
A Gene-for-Gene Relationship Between Wheat and Mycosphaerella graminicola, the Septoria Tritici Blotch Pathogen
inferred← citeshttps://doi.org/10.1094/phyto.2004.94.7.743openalex-snapshot
Genetic Characterization of Cercospora sorghi from Cultivated and Wild Sorghum and Its Relationship to Other Cercospora Fungi
inferred← citeshttps://doi.org/10.1094/phytofr-06-25-0058-aopenalex-snapshot
Draft Genome Sequence Resource of the Citrus Greasy Spot Fungal Pathogen Zasmidium citri-griseum Isolate MCC3
inferred← citeshttps://doi.org/10.1098/rspb.2016.0812openalex-snapshot
Marine Phytophthora species can hamper conservation and restoration of vegetated coastal ecosystems
inferred← citeshttps://doi.org/10.1100/2012/368286openalex-snapshot
Genetic Diversity and Population Differentiation of the Causal Agent of Citrus Black Spot in Brazil
inferred← citeshttps://doi.org/10.1111/1758-2229.70200openalex-snapshot
Insights Into the Mondia Whitei Microbiome Across Geographic Regions in Eastern Africa
inferred← citeshttps://doi.org/10.1111/efp.12290openalex-snapshot
Global geographic distribution and host range of Dothistroma species: a comprehensive review
inferred← citeshttps://doi.org/10.1111/j.1364-3703.2004.00218.xopenalex-snapshot
Sugarbeet leaf spot disease ( Cercospora beticola Sacc.)†
inferred← citeshttps://doi.org/10.1111/j.1364-3703.2004.00239.xopenalex-snapshot
Recognition of Cladosporium fulvum Ecp2 elicitor by non‐host Nicotiana spp. is mediated by a single dominant gene that is not homologous to known Cf ‐genes
inferred← citeshttps://doi.org/10.1111/j.1364-3703.2005.00292.xopenalex-snapshot
Cladosporium fulvum (syn. Passalora fulva ), a highly specialized plant pathogen as a model for functional studies on plant pathogenic Mycosphaerellaceae
inferred← citeshttps://doi.org/10.1111/j.1364-3703.2006.00376.xopenalex-snapshot
Isolation and characterization of the mating type locus of Mycosphaerella fijiensis , the causal agent of black leaf streak disease of banana
inferred← citeshttps://doi.org/10.1111/j.1364-3703.2008.00516.xopenalex-snapshot
Teratosphaeria nubilosa , a serious leaf disease pathogen of Eucalyptus spp. in native and introduced areas
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2012.05714.xopenalex-snapshot
Cryptic species, native populations and biological invasions by a eucalypt forest pathogen
inferred← citeshttps://doi.org/10.1111/j.1365-3059.2007.01697.xopenalex-snapshot
Indirect evidence for sexual reproduction in Cercospora beticola populations from sugar beet
inferred← citeshttps://doi.org/10.1111/j.1365-3059.2008.01892.xopenalex-snapshot
A method of inoculating barley seedlings with Ramularia collo‐cygni
inferred← citeshttps://doi.org/10.1111/j.1365-3059.2008.01962.xopenalex-snapshot
Occurrence of Cercospora cantuariensis on hop in Austria and Slovenia
inferred← citeshttps://doi.org/10.1111/j.1365-3059.2008.01988.xopenalex-snapshot
Identification and genetic diversity of Mycosphaerella species on banana and plantain in Nigeria
inferred← citeshttps://doi.org/10.1111/j.1439-0329.2004.00356.xopenalex-snapshot
Dothistroma (red‐band) needle blight of pines and the dothistromin toxin: a review
inferred← citeshttps://doi.org/10.1111/j.1439-0434.2006.01080.xopenalex-snapshot
Analysis of β‐tubulin Gene Fragments from Benzimidazole‐sensitive and ‐tolerant Cercospora beticola
inferred← citeshttps://doi.org/10.1111/j.1439-0434.2011.01862.xopenalex-snapshot
Evaluation of Hydrangea macrophylla for Resistance to Leaf‐Spot Diseases
inferred← citeshttps://doi.org/10.1111/mpp.12962openalex-snapshot
Cercospora beticola: The intoxicating lifestyle of the leaf spot pathogen of sugar beet
inferred← citeshttps://doi.org/10.1111/ppa.13337openalex-snapshot
Dynamics of cercospora leaf spot disease determined by aerial spore dispersal in artificially inoculated sugar beet fields
inferred← citeshttps://doi.org/10.1111/ppa.13956openalex-snapshot
Cercospora leaf blight and purple seed stain of soybean: A permanent challenge
inferred← citeshttps://doi.org/10.1139/b04-070openalex-snapshot
Devriesia, a new hyphomycete genus to accommodate heat-resistant, cladosporium-like fungi
inferred← citeshttps://doi.org/10.1139/b10-015openalex-snapshot
Two new dothideomycetous endoconidial genera from declining larch
inferred← citeshttps://doi.org/10.1177/1934578x1100600620openalex-snapshot
Chemical Constituents of the New Endophytic Fungus Mycosphaerella sp. nov. and Their Anti-parasitic Activity
inferred← citeshttps://doi.org/10.1186/1471-2164-14-78openalex-snapshot
Analysis of the leaf transcriptome of Musa acuminata during interaction with Mycosphaerella musicola: gene assembly, annotation and marker development
inferred← citeshttps://doi.org/10.1186/s12866-020-01853-0openalex-snapshot
Comparative transcriptome analysis of two Cercospora sojina strains reveals differences in virulence under nitrogen starvation stress
inferred← citeshttps://doi.org/10.1186/s13104-020-05328-3openalex-snapshot
Draft genome assembly of Passalora sequoiae a needle blight pathogen on Leyland cypress
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003088openalex-snapshot
The Genomes of the Fungal Plant Pathogens Cladosporium fulvum and Dothistroma septosporum Reveal Adaptation to Different Hosts and Lifestyles But Also Signatures of Common Ancestry
inferred← citeshttps://doi.org/10.1371/journal.pone.0133495openalex-snapshot
More Cercospora Species Infect Soybeans across the Americas than Meets the Eye
inferred← citeshttps://doi.org/10.14199/ppp-2019-002openalex-snapshot
Cercospora leaf spot of sugar beet (Cercospora beticola Sacc.) Part I. Biology and occurrence
inferred← citeshttps://doi.org/10.14393/ufu.te.2023.637openalex-snapshot
Padronização dos métodos de análises da cercosporina e isocercosporina do extrato de Cercospora brachiata e avaliação da atividade herbicida e de danos à biomembranas de lipossomas
inferred← citeshttps://doi.org/10.14601/phytopathol_mediterr-16230openalex-snapshot
Trail of decryption of molecular research on Botryosphaeriaceae in woody plants
inferred← citeshttps://doi.org/10.14601/phytopathol_mediterr-9009openalex-snapshot
Uneven distribution of mating type alleles in Iranian populations of Cercospora beticola , the causal agent of Cercospora leaf spot disease of sugar beet
inferred← citeshttps://doi.org/10.15517/am.v33i3.48494openalex-snapshot
Tizón Foliar y la Mancha Púrpura de la semilla causados por Cercospora kikuchii en soja (Glycine max L. Merr.)
inferred← citeshttps://doi.org/10.1590/s0100-41582005000600005openalex-snapshot
Pathogenicity, molecular characterization, and cercosporin content of Brazilian isolates of Cercospora kikuchii
inferred← citeshttps://doi.org/10.1590/s1415-47572008005000010openalex-snapshot
Molecular variability in the maize grey leaf spot pathogens in Brazil
inferred← citeshttps://doi.org/10.1590/s1982-56762011000500007openalex-snapshot
Variabilidade in vitro, in vivo e molecular de isolados de Cercospora coffeicola
inferred← citeshttps://doi.org/10.17221/4484-jfsopenalex-snapshot
The host spectrum of Dothistroma needle blight Mycosphaerella pini E. Rostrup - new hosts of Dothistroma needle blight observed in theCzech Republic
inferred← citeshttps://doi.org/10.18174/121595openalex-snapshot
Recognition of the Cladosporium fulvum Ecp2 elicitor in tomato and non-host plants
inferred← citeshttps://doi.org/10.18174/121995openalex-snapshot
Phylogeny, detection, and mating behaviour of Mycosphaerella spp. occurring on banana
inferred← citeshttps://doi.org/10.18174/122004openalex-snapshot
Cladosporium fulvum effector proteins and their role in pathogen virulence
inferred← citeshttps://doi.org/10.18174/23015openalex-snapshot
Molecular characterization of Cercospora beticola and its relatives
inferred← citeshttps://doi.org/10.18174/25117openalex-snapshot
Drug transporters of the fungal wheat pathogen Mycosphaerella graminicola
inferred← citeshttps://doi.org/10.18174/301336openalex-snapshot
Comparative genomics of Dothideomycete fungi
inferred← citeshttps://doi.org/10.22092/botany.2012.101391openalex-snapshot
اطلاعات جدید درباره گونههای Cercospora و Pseudocercospora از استان گیلان
inferred← citeshttps://doi.org/10.2307/3762175openalex-snapshot
Phylogenetic Analyses of Septoria Species Based on the ITS and LSU-D2 Regions of Nuclear Ribosomal DNA
inferred← citeshttps://doi.org/10.3114/sim.2007.58.01openalex-snapshot
Mycosphaerella is polyphyletic
inferred← citeshttps://doi.org/10.3114/sim.2022.101.06openalex-snapshot
Genera of phytopathogenic fungi: GOPHY 4
inferred← citeshttps://doi.org/10.3114/sim.2024.108.01openalex-snapshot
What are the 100 most cited fungal genera?
inferred← citeshttps://doi.org/10.3114/sim.55.1.189openalex-snapshot
Species of Cercospora associated with grey leaf spot of maize
inferred← citeshttps://doi.org/10.3114/sim0012openalex-snapshot
Species concepts in Cercospora: spotting the weeds among the roses
inferred← citeshttps://doi.org/10.3114/sim0018openalex-snapshot
A new approach to species delimitation in Septoria
inferred← citeshttps://doi.org/10.3119/22-16openalex-snapshot
Epidemiology and Effects of a Leaf Spot Disease in Veratrum viride (Melanthiaceae)
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.2140openalex-snapshot
Evolutionary Relationships among Fungal Soybean Pathogens and Molecular Marker Development in the Genus Cercospora
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.3002openalex-snapshot
Molecular Approaches to Detect and Control Cercospora kikuchii in Soybeans
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.4239openalex-snapshot
The roles of AVR4 in fungal virulence,cercosporin biosynthesis and its potential use in host induced gene silencing for controlling cercospora leaf blight disease of soybeans
inferred← citeshttps://doi.org/10.3168/jds.2017-13754openalex-snapshot
Bacterial and fungal communities, fermentation, and aerobic stability of conventional hybrids and brown midrib hybrids ensiled at low moisture with or without a homo- and heterofermentative inoculant
inferred← citeshttps://doi.org/10.3389/fpls.2024.1404483openalex-snapshot
Recent advances in the population biology and management of maize foliar fungal pathogens Exserohilum turcicum, Cercospora zeina and Bipolaris maydis in Africa
inferred← citeshttps://doi.org/10.3389/fpls.2025.1605156openalex-snapshot
Real-time quantitative PCR method for assessing wheat cultivars for resistance to Zymoseptoria tritici
inferred← citeshttps://doi.org/10.3390/ijms21228555openalex-snapshot
Phytopathogenic Cercosporoid Fungi—From Taxonomy to Modern Biochemistry and Molecular Biology
inferred← citeshttps://doi.org/10.3390/jof10110802openalex-snapshot
Population Structure and Mating Type Distribution of Cercospora sojina from Soybeans in Indiana, United States
inferred← citeshttps://doi.org/10.35537/10915/120973openalex-snapshot
Hongos causantes de la mancha gris de la hoja en Lycopersicon esculentum Mill., su variabilidad y el rol de la resistencia sistémica adquirida (RSA) en la reducción de su incidencia
inferred← citeshttps://doi.org/10.35537/10915/127606openalex-snapshot
Sensibilidad y resistencia a fungicidas de Cercospora kikuchii, agente causal del tizón de la hoja y mancha púrpura de la semilla de la soja
inferred← citeshttps://doi.org/10.36961/si23837openalex-snapshot
Catch me if you can – Auf der Spur der Cercospora-Sporen
inferred← citeshttps://doi.org/10.37045/aslh-2007-0009openalex-snapshot
The Contemporary Situation of Dothistroma Needle Blight Outbreak in the Czech Republic
inferred← citeshttps://doi.org/10.3767/003158508x302212openalex-snapshot
Multiple gene genealogies and phenotypic characters differentiate several novel species of Mycosphaerella and related anamorphs on banana
inferred← citeshttps://doi.org/10.3767/003158508x323949openalex-snapshot
Host specificity and speciation of Mycosphaerella and Teratosphaeria species associated with leaf spots of Proteaceae
inferred← citeshttps://doi.org/10.3767/003158508x380612openalex-snapshot
Foliicolous microfungi occurring on Encephalartos
inferred← citeshttps://doi.org/10.3767/003158509x479487openalex-snapshot
Unravelling Mycosphaerella: do you believe in genera?
inferred← citeshttps://doi.org/10.3767/003158509x479531openalex-snapshot
Novel species of Mycosphaerellaceae and Teratosphaeriaceae
inferred← citeshttps://doi.org/10.3767/003158511x571841openalex-snapshot
Zymoseptoria gen. nov.: a new genus to accommodate Septoria- like species occurring on graminicolous hosts
inferred← citeshttps://doi.org/10.3767/003158514x681981openalex-snapshot
Introducing the Consolidated Species Concept to resolve species in the Teratosphaeriaceae
inferred← citeshttps://doi.org/10.3767/003158515x685698openalex-snapshot
Application of the consolidated species concept to Cercospora spp. from Iran
inferred← citeshttps://doi.org/10.3767/003158516x690934openalex-snapshot
Novel fungi from an ancient niche: cercosporoid and related sexual morphs on ferns
inferred← citeshttps://doi.org/10.3852/10-184openalex-snapshot
Genetic diversity and population structure in French populations ofMycosphaerella graminicola
inferred← citeshttps://doi.org/10.3852/12-371openalex-snapshot
Phytophthora terminalis sp. nov. and Phytophthora occultans sp. nov., two invasive pathogens of ornamental plants in Europe
inferred← citeshttps://doi.org/10.3852/13-147openalex-snapshot
Porocercospora seminalis gen . et comb. nov., the causal organism of buffalograss false smut
inferred← citeshttps://doi.org/10.3852/mycologia.97.2.349openalex-snapshot
Malazy, a degenerate, species-specific transposable element in Cercospora zeae-maydis
inferred← citeshttps://doi.org/10.3852/mycologia.97.5.1122openalex-snapshot
Cercosporella acroptili and Cercosporella centaureicola sp. nov.--potential biological control agents of Russian knapweed and yellow starthistle, respectively
inferred← citeshttps://doi.org/10.3852/mycologia.98.2.275openalex-snapshot
Host range of Cercospora apii and C. beticola and description of C. apiicola, a novel species from celery
inferred← citeshttps://doi.org/10.3852/mycologia.99.2.240openalex-snapshot
The systematic position of Phaeocryptopus gaeumannii
inferred← citeshttps://doi.org/10.3929/ethz-a-005807786openalex-snapshot
Mitochondrial genomes of plant pathogenic fungi
inferred← citeshttps://doi.org/10.5423/ppj.2010.26.3.289openalex-snapshot
Simple and Reliable DNA Extraction Method for the Dark Pigmented Fungus, Cercospora sojina
inferred← citeshttps://doi.org/10.5423/ppj.2011.27.2.103openalex-snapshot
Regulation of Pathogenesis by Light in Cercospora zeae-maydis: An Updated Perspective
inferred← citeshttps://doi.org/10.5423/ppj.2011.27.2.183openalex-snapshot
Differential Responses of Soybean Cultivars to Cercospora sojina Isolates, the Causal Agent of Frogeye Leaf Spot in Korea
inferred← citeshttps://doi.org/10.5598/imafungus.2013.04.02.12openalex-snapshot
Cercosporoid fungi (Mycosphaerellaceae) 1. Species on other fungi, Pteridophyta and Gymnospermae
inferred← citeshttps://doi.org/10.5598/imafungus.2014.05.02.04openalex-snapshot
Cercosporoid fungi (Mycosphaerellaceae) 2. Species on monocots (Acoraceae to Xyridaceae, excluding Poaceae)
inferred← citeshttps://doi.org/10.5598/imafungus.2015.06.01.03openalex-snapshot
Cercosporoid fungi (Mycosphaerellaceae) 3. Species on monocots (Poaceae, true grasses)
inferred← citeshttps://doi.org/10.5598/imafungus.2018.09.02.06openalex-snapshot
Novel primers improve species delimitation in Cercospora
inferred← citeshttps://doi.org/10.5897/ajb11.2966openalex-snapshot
Cloning, in silico structural characterization and expression analysis of MfAtr4, an ABC transporter from the banana pathogen Mycosphaerella fijiensis
inferred← citeshttps://doi.org/10.5897/ajmr12.205openalex-snapshot
Investigation of genetic variability among different isolates of Fusarium solani
inferred← citeshttps://doi.org/10.5943/ppq/2/1/7openalex-snapshot
Comprehensive check list of Cercosporoid fungi from Iran
inferred← citeshttps://doi.org/10.5943/ppq/2/2/5openalex-snapshot
Morphological and molecular characterization of Cercospora zebrina from black bindweed in Iran
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