Rapidly Evolving Genes Are Key Players in Host Specialization and Virulence of the Fungal Wheat Pathogen Zymoseptoria tritici (Mycosphaerella graminicola).
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Using Population and Comparative Genomics to Understand the Genetic Basis of Effector-Driven Fungal Pathogen EvolutionThe genetic basis of local adaptation for pathogenic fungi in agricultural ecosystems.The Evolution of Orphan Regions in Genomes of a Fungal Pathogen of Wheat.Pathogen effectors and plant immunity determine specialization of the blast fungus to rice subspecies.Utilizing Gene Tree Variation to Identify Candidate Effector Genes in Zymoseptoria tritici.Genetic Adaptation of Giant Lobelias (Lobelia aberdarica and Lobelia telekii) to Different Altitudes in East African MountainsComparative transcriptomic analyses of Zymoseptoria tritici strains show complex lifestyle transitions and intraspecific variability in transcription profiles.In silico prediction and characterization of secondary metabolite biosynthetic gene clusters in the wheat pathogen Zymoseptoria tritici.Evaluation of Secretion Prediction Highlights Differing Approaches Needed for Oomycete and Fungal Effectors.The escalatory Red Queen: Population extinction and replacement following arms race dynamics in poplar rust.A Review of Conventional PCR Assays for the Detection of Selected Phytopathogens of Wheat.Forward Genetics Approach Reveals Host Genotype-Dependent Importance of Accessory Chromosomes in the Fungal Wheat Pathogen Zymoseptoria tritici.A fungal wheat pathogen evolved host specialization by extensive chromosomal rearrangements.Positively selected effector genes and their contribution to virulence in the smut fungus Sporisorium reilianum.Comparative Genomics of Smut Pathogens: Insights From Orphans and Positively Selected Genes Into Host Specialization.Comparative Methods for Molecular Determination of Host-Specificity Factors in Plant-Pathogenic Fungi.Quantitative trait locus mapping reveals complex genetic architecture of quantitative virulence in the wheat pathogen Zymoseptoria tritici.A fungal avirulence factor encoded in a highly plastic genomic region triggers partial resistance to septoria tritici blotch.Genome-wide evidence for divergent selection between populations of a major agricultural pathogen.Whole-Genome Resequencing and Pan-Transcriptome Reconstruction Highlight the Impact of Genomic Structural Variation on Secondary Metabolite Gene Clusters in the Grapevine Esca Pathogen
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P2860
Rapidly Evolving Genes Are Key Players in Host Specialization and Virulence of the Fungal Wheat Pathogen Zymoseptoria tritici (Mycosphaerella graminicola).
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
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2015年论文
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name
Rapidly Evolving Genes Are Key ...... (Mycosphaerella graminicola).
@ast
Rapidly Evolving Genes Are Key ...... (Mycosphaerella graminicola).
@en
type
label
Rapidly Evolving Genes Are Key ...... (Mycosphaerella graminicola).
@ast
Rapidly Evolving Genes Are Key ...... (Mycosphaerella graminicola).
@en
prefLabel
Rapidly Evolving Genes Are Key ...... (Mycosphaerella graminicola).
@ast
Rapidly Evolving Genes Are Key ...... (Mycosphaerella graminicola).
@en
P2093
P2860
P1433
P1476
Rapidly Evolving Genes Are Key ...... (Mycosphaerella graminicola).
@en
P2093
Lena Dorsheimer
Petra Happel
Stephan Poppe
P2860
P304
P356
10.1371/JOURNAL.PPAT.1005055
P577
2015-07-30T00:00:00Z