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Transcriptional Enhancement of Pathogenicity Genes in the Pep Cluster is Influenced by a Pisatin-Responsive Gene (Prg1) in Fusarium Vanettenii and Contributes to Virulence on Garden Pea
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/abbi.1996.0346openalex-extracted
Identification of a NovelpelDGene Expressed Uniquely in Planta byFusarium solanif. sp.pisi(Nectria haematococca,Mating Type VI) and Characterization of Its Protein Product as an Endo-Pectate Lyase
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-extracted
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/978-1-0716-1795-3_7openalex-extracted
Targeted Gene Disruption Via CRISPR/Cas9 Ribonucleoprotein Complexes in Fusarium oxysporum
inferredcites →https://doi.org/10.1007/bf00284198openalex-extracted
A gene from the fungal plant pathogen Nectria haematococca that encodes the phytoalexin-detoxifying enzyme pisatin demethylase defines a new cytochrome P450 family
inferredcites →https://doi.org/10.1007/bf02191822openalex-extracted
Identification of elements in thePDA1 promoter ofNectria haematococca necessary for a high level of transcription in vitro
inferredcites →https://doi.org/10.1007/s00294-002-0279-xopenalex-extracted
Distribution of the pea pathogenicity (PEP) genes in the fungus Nectria haematococca mating population VI
inferredcites →https://doi.org/10.1007/s00294-003-0428-xopenalex-extracted
Expression profiles of pea pathogenicity (PEP) genes in vivo and in vitro, characterization of the flanking regions of the PEP cluster and evidence that the PEP cluster region resulted from horizontal gene transfer in the fungal pathogen Nectria haematococca
inferredcites →https://doi.org/10.1007/s00294-004-0506-8openalex-extracted
An analysis of the phylogenetic distribution of the pea pathogenicity genes of Nectria haematococca MPVI supports the hypothesis of their origin by horizontal transfer and uncovers a potentially new pathogen of garden pea: Neocosmospora boniensis
inferredcites →https://doi.org/10.1016/0048-4059(80)90040-5openalex-extracted
The association of pisatin tolerance and demethylation with virulence on pea in Nectria haematococca
inferredcites →https://doi.org/10.1016/j.fgb.2018.05.003openalex-extracted
Efficient genome editing in Fusarium oxysporum based on CRISPR/Cas9 ribonucleoprotein complexes
inferredcites →https://doi.org/10.1016/j.tplants.2011.11.002openalex-extracted
Phytoalexins in defense against pathogens
inferredcites →https://doi.org/10.1038/191076a0openalex-extracted
Pisatin: an Antifungal Substance from Pisum sativum L.
inferredcites →https://doi.org/10.1038/s41586-021-03819-2openalex-extracted
Highly accurate protein structure prediction with AlphaFold
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03552.xopenalex-extracted
A binuclear zinc transcription factor binds the host isoflavonoid‐responsive element in a fungal cytochrome p450 gene responsible for detoxification
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00969.xopenalex-extracted
Genes determining pathogenicity to pea are clustered on a supernumerary chromosome in the fungal plant pathogen Nectria haematococca
inferredcites →https://doi.org/10.1093/bfgp/3.2.125openalex-extracted
The roles of cytoplasmic poly(A)-binding proteins in regulating gene expression: A developmental perspective
inferredcites →https://doi.org/10.1093/nar/gkh131openalex-extracted
UniProt: the Universal Protein knowledgebase
inferredcites →https://doi.org/10.1093/nar/gkm259openalex-extracted
WoLF PSORT: protein localization predictor
inferredcites →https://doi.org/10.1093/nar/gkq477openalex-extracted
YLoc—an interpretable web server for predicting subcellular localization
inferredcites →https://doi.org/10.1094/mpmi-09-10-0198openalex-extracted
An ABC Transporter and a Cytochrome P450 of Nectria haematococca MPVI Are Virulence Factors on Pea and Are the Major Tolerance Mechanisms to the Phytoalexin Pisatin
inferredcites →https://doi.org/10.1094/mpmi-9-0793openalex-extracted
Transformation-Mediated Chromosome Loss and Disruption of a Gene for Pisatin Demethylase Decrease the Virulence ofNectria haematococcaon Pea
inferredcites →https://doi.org/10.1094/mpmi.1999.12.8.733openalex-extracted
Regulatory Signals Influencing Expression of the PDA1 Gene of Nectria haematococca MPVI in Culture and During Pathogenesis of Pea
inferredcites →https://doi.org/10.1094/phyto-08-20-0330-leopenalex-extracted
Phylogenomic Analysis of a 55.1-kb 19-Gene Dataset Resolves a MonophyleticFusariumthat Includes theFusarium solaniSpecies Complex
inferredcites →https://doi.org/10.1094/phyto-68-1552openalex-extracted
Identification of Additional Habitats of Nectria haematococca Mating Population VI
inferredcites →https://doi.org/10.1101/gad.888601openalex-extracted
TEAD/TEF transcription factors utilize the activation domain of YAP65, a Src/Yes-associated protein localized in the cytoplasm
inferredcites →https://doi.org/10.1111/mpp.12289openalex-extracted
The F usarium solani species complex: ubiquitous pathogens of agricultural importance
inferredcites →https://doi.org/10.1111/mpp.13056openalex-extracted
Transcription factor control of virulence in phytopathogenic fungi
inferredcites →https://doi.org/10.1186/1471-2105-10-274openalex-extracted
MultiLoc2: integrating phylogeny and Gene Ontology terms improves subcellular protein localization prediction
inferredcites →https://doi.org/10.1371/journal.pgen.1000618openalex-extracted
The Genome of Nectria haematococca: Contribution of Supernumerary Chromosomes to Gene Expansion
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