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Investigations on VELVET regulatory mutants confirm the role of host tissue acidification and secretion of proteins in the pathogenesis of Botrytis cinerea
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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/pmic.201000037openalex-snapshot
The Botrytis cinerea early secretome
inferredcites →https://doi.org/10.1007/978-1-4614-2356-0_24openalex-snapshot
Proteomic Protocols for the Study of Filamentous Fungi
inferredcites →https://doi.org/10.1007/s00253-013-5132-2openalex-snapshot
Metabolic engineering of Aspergillus oryzae NRRL 3488 for increased production of l-malic acid
inferredcites →https://doi.org/10.1016/0003-2697(84)90782-6openalex-snapshot
A method for the quantitative recovery of protein in dilute solution in the presence of detergents and lipids
inferredcites →https://doi.org/10.1016/0885-5765(90)90061-2openalex-snapshot
The roles of aspartic proteinase and endo-pectin lyase enzymes in the primary stages of infection and pathogenesis of various host tissues by different isolates of Botrytis cinerea Pers ex. Pers
inferredcites →https://doi.org/10.1016/j.bbrc.2015.01.038openalex-snapshot
BcGs1, a glycoprotein from Botrytis cinerea , elicits defence response and improves disease resistance in host plants
inferredcites →https://doi.org/10.1016/j.fgb.2009.10.008openalex-snapshot
The Botrytis cinerea aspartic proteinase family
inferredcites →https://doi.org/10.1016/j.fgb.2012.10.003openalex-snapshot
Involvement of BcVeA and BcVelB in regulating conidiation, pigmentation and virulence in Botrytis cinerea
inferredcites →https://doi.org/10.1016/j.plantsci.2014.12.018openalex-snapshot
Pathogenic attributes of Sclerotinia sclerotiorum : Switching from a biotrophic to necrotrophic lifestyle
inferredcites →https://doi.org/10.1016/j.pmpp.2010.06.003openalex-snapshot
Functional analysis and mode of action of phytotoxic Nep1-like proteins of Botrytis cinerea
inferredcites →https://doi.org/10.1016/s0168-6496(02)00439-7openalex-snapshot
Differential regulation by ambient pH of putative virulence factor secretion by the phytopathogenic fungus Botrytis cinerea
inferredcites →https://doi.org/10.1016/s0960-9822(00)00560-1openalex-snapshot
The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea
inferredcites →https://doi.org/10.1021/pr300365fopenalex-snapshot
Exploring Pathogenic Mechanisms of Botrytis cinerea Secretome under Different Ambient pH Based on Comparative Proteomic Analysis
inferredcites →https://doi.org/10.1042/bj20140001openalex-snapshot
In vitrocharacterization of bacterial and chloroplast Hsp70 systems reveals an evolutionary optimization of the co-chaperones for their Hsp70 partner
inferredcites →https://doi.org/10.1074/jbc.m608961200openalex-snapshot
Oxaloacetate Hydrolase, the C–C Bond Lyase of Oxalate Secreting Fungi
inferredcites →https://doi.org/10.1093/bioinformatics/btl633openalex-snapshot
Enrichment or depletion of a GO category within a class of genes: which test?
inferredcites →https://doi.org/10.1094/mpmi-02-14-0036-ropenalex-snapshot
The Endo-Arabinanase BcAra1 Is a Novel Host-Specific Virulence Factor of the Necrotic Fungal Phytopathogen Botrytis cinerea
inferredcites →https://doi.org/10.1094/mpmi-04-15-0074-ropenalex-snapshot
Synergistic Action of a Metalloprotease and a Serine Protease from Fusarium oxysporum f. sp. lycopersici Cleaves Chitin-Binding Tomato Chitinases, Reduces Their Antifungal Activity, and Enhances Fungal Virulence
inferredcites →https://doi.org/10.1094/mpmi-12-14-0411-ropenalex-snapshot
The VELVET Complex in the Gray Mold FungusBotrytis cinerea: Impact of BcLAE1 on Differentiation, Secondary Metabolism, and Virulence
inferredcites →https://doi.org/10.1094/mpmi.1998.11.10.1009openalex-snapshot
The Endopolygalacturonase Gene Bcpg1 Is Required for Full Virulence of Botrytis cinerea
inferredcites →https://doi.org/10.1099/mic.0.025999-0openalex-snapshot
pH controls both transcription and post-translational processing of the protease BcACP1 in the phytopathogenic fungus Botrytis cinerea
inferredcites →https://doi.org/10.1099/mic.0.27058-0openalex-snapshot
An aspartic proteinase gene family in the filamentous fungus Botrytis cinerea contains members with novel features
inferredcites →https://doi.org/10.1104/pp.17.00375openalex-snapshot
BcXYG1, a Secreted Xyloglucanase from Botrytis cinerea , Triggers Both Cell Death and Plant Immune Responses
inferredcites →https://doi.org/10.1105/tpc.12.11.2191openalex-snapshot
Oxalic Acid, a Pathogenicity Factor for Sclerotinia sclerotiorum, Suppresses the Oxidative Burst of the Host Plant
inferredcites →https://doi.org/10.1111/1462-2920.12818openalex-snapshot
pH dependency of sclerotial development and pathogenicity revealed by using genetically defined oxalate‐minus mutants of S clerotinia sclerotiorum
inferredcites →https://doi.org/10.1111/j.1364-3703.2010.00692.xopenalex-snapshot
The Botrytis cinerea phytotoxin botcinic acid requires two polyketide synthases for production and has a redundant role in virulence with botrydial
inferredcites →https://doi.org/10.1111/j.1364-3703.2011.00772.xopenalex-snapshot
pH modulation differs during sunflower cotyledon colonization by the two closely related necrotrophic fungi Botrytis cinerea and Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1111/j.1364-3703.2011.00783.xopenalex-snapshot
The Top 10 fungal pathogens in molecular plant pathology
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05506.xopenalex-snapshot
Aspergillus nidulans VeA subcellular localization is dependent on the importin α carrier and on light
inferredcites →https://doi.org/10.1111/j.1365-2958.2012.08083.xopenalex-snapshot
The putative protein methyltransferase LAE1 controls cellulase gene expression in Trichoderma reesei
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02436.xopenalex-snapshot
Necrotizing activity of five Botrytis cinerea endopolygalacturonases produced in Pichia pastoris
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04553.xopenalex-snapshot
A critical role of autophagy in plant resistance to necrotrophic fungal pathogens
inferredcites →https://doi.org/10.1111/j.1439-0434.1988.tb01024.xopenalex-snapshot
Changes in pH and the Production of Organic Acids During Colonization of Tomato Petioles by Botrytis cinerea
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01682.xopenalex-snapshot
Characterization of a new, nonpathogenic mutant of Botrytis cinerea with impaired plant colonization capacity
inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00285.xopenalex-snapshot
Coordination of secondarymetabolism and development in fungi: the velvet familyof regulatory proteins
inferredcites →https://doi.org/10.1111/mpp.12211openalex-snapshot
Oxaloacetate acetylhydrolase gene mutants of S clerotinia sclerotiorum do not accumulate oxalic acid, but do produce limited lesions on host plants
inferredcites →https://doi.org/10.1111/mpp.12384openalex-snapshot
A gapless genome sequence of the fungus Botrytis cinerea
inferredcites →https://doi.org/10.1111/nph.14588openalex-snapshot
The Botrytis cinerea elicitor protein BcIEB1 interacts with the tobacco PR5‐family protein osmotin and protects the fungus against its antifungal activity
inferredcites →https://doi.org/10.1126/science.1155888openalex-snapshot
VelB/VeA/LaeA Complex Coordinates Light Signal with Fungal Development and Secondary Metabolism
inferredcites →https://doi.org/10.1128/ec.00295-12openalex-snapshot
Transcriptome Profiling of Botrytis cinerea Conidial Germination Reveals Upregulation of Infection-Related Genes during the Prepenetration Stage
inferredcites →https://doi.org/10.1146/annurev-phyto-082712-102349openalex-snapshot
Quiescent and Necrotrophic Lifestyle Choice During Postharvest Disease Development
inferredcites →https://doi.org/10.1186/1471-2229-10-38openalex-snapshot
The Botrytis cinerea xylanase Xyn11A contributes to virulence with its necrotizing activity, not with its catalytic activity
inferredcites →https://doi.org/10.1371/journal.pbio.1001750openalex-snapshot
The Velvet Family of Fungal Regulators Contains a DNA-Binding Domain Structurally Similar to NF-κB
inferredcites →https://doi.org/10.1371/journal.pgen.1002230openalex-snapshot
Genomic Analysis of the Necrotrophic Fungal Pathogens Sclerotinia sclerotiorum and Botrytis cinerea
inferredcites →https://doi.org/10.1371/journal.pone.0047840openalex-snapshot
Natural Variation in the VELVET Gene bcvel1 Affects Virulence and Light-Dependent Differentiation in Botrytis cinerea
inferredcites →https://doi.org/10.1371/journal.pone.0053729openalex-snapshot
A Functional Bikaverin Biosynthesis Gene Cluster in Rare Strains of Botrytis cinerea Is Positively Controlled by VELVET
inferredcites →https://doi.org/10.1371/journal.pone.0089883openalex-snapshot
VelC Positively Controls Sexual Development in Aspergillus nidulans
inferredcites →https://doi.org/10.1371/journal.ppat.1002107openalex-snapshot
Tipping the Balance: Sclerotinia sclerotiorum Secreted Oxalic Acid Suppresses Host Defenses by Manipulating the Host Redox Environment
inferredcites →https://doi.org/10.1371/journal.ppat.1003287openalex-snapshot
Cell Death Control: The Interplay of Apoptosis and Autophagy in the Pathogenicity of Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1534/g3.115.024067openalex-snapshot
Identification of a Classical Mutant in the Industrial Host Aspergillus niger by Systems Genetics: LaeA Is Required for Citric Acid Production and Regulates the Formation of Some Secondary Metabolites
inferredcites →https://doi.org/10.3389/fmicb.2015.00001openalex-snapshot
One Juliet and four Romeos: VeA and its methyltransferases
inferredcites →https://doi.org/10.3389/fpls.2016.01306openalex-snapshot
How Does Host Carbon Concentration Modulate the Lifestyle of Postharvest Pathogens during Colonization?
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.4830909openalex-extracted
The Vacuolar H+-Atpase Subunit C is Involved in Oligogalacturonide (Og) Internalization and Og-Triggered Immunity
inferred← citeshttps://doi.org/10.1002/jsfa.9827openalex-snapshot
Botrytis cinerea differentially induces postharvest antioxidant responses in ‘Braeburn’ and ‘Golden Delicious’ apple fruit
inferred← citeshttps://doi.org/10.1007/978-3-031-16503-0_14openalex-snapshot
Role of Light in the Life Cycle of Botrytis cinerea
inferred← citeshttps://doi.org/10.1007/978-981-99-4890-1_11openalex-snapshot
Exploring Plant-Pathogen Interactions through Subcellular Proteomics: Insights and Challenges
inferred← citeshttps://doi.org/10.1007/s44154-024-00183-9openalex-snapshot
Plant–pathogen interactions and ambient pH dynamics
inferred← citeshttps://doi.org/10.1016/j.cej.2025.168723openalex-snapshot
Adaptive response platforms in smart packaging: Endogenous triggering and exogenous activation enable dynamic release of active substances to preserve postharvest fruits and vegetables
inferred← citeshttps://doi.org/10.1016/j.cej.2026.174044openalex-snapshot
Adhesive and redox modulatory nanopesticides with pathogenic microenvironment-regulated multi-enzymatic activities for synergistic control of ginseng gray mold
inferred← citeshttps://doi.org/10.1016/j.fgb.2018.11.003openalex-snapshot
The putative H3K36 demethylase BcKDM1 affects virulence, stress responses and photomorphogenesis in Botrytis cinerea
inferred← citeshttps://doi.org/10.1016/j.fgb.2020.103445openalex-snapshot
Penicillium oxalicum putative methyltransferase Mtr23B has similarities and differences with LaeA in regulating conidium development and glycoside hydrolase gene expression
inferred← citeshttps://doi.org/10.1016/j.foodchem.2023.135443openalex-snapshot
Propionate poses antivirulence activity against Botrytis cinerea via regulating its metabolism, infection cushion development and overall pathogenic factors
inferred← citeshttps://doi.org/10.1016/j.funbio.2020.01.004openalex-snapshot
Light sensing in plant- and rock-associated black fungi
inferred← citeshttps://doi.org/10.1016/j.jprot.2019.103580openalex-snapshot
Comparative quantitative proteomics of osmotic signal transduction mutants in Botrytis cinerea explain mutant phenotypes and highlight interaction with cAMP and Ca2+ signalling pathways
inferred← citeshttps://doi.org/10.1016/j.micres.2021.126752openalex-snapshot
Insights into the multitrophic interactions between the biocontrol agent Bacillus subtilis MBI 600, the pathogen Botrytis cinerea and their plant host
inferred← citeshttps://doi.org/10.1016/j.molp.2025.12.019openalex-snapshot
Activation of multilayered plant immunity through spatiotemporal expression of Botrytis cinerea BcCrh1-derived dual epitopes
inferred← citeshttps://doi.org/10.1016/j.pestbp.2021.104884openalex-snapshot
Potential value of small-molecule organic acids for the control of postharvest gray mold caused by Botrytis cinerea
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113134openalex-snapshot
Gas5A, a putative glucanosyltransferase from Botrytis, functions as cell death inducing protein in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109117openalex-snapshot
The Vacuolar H+-ATPase subunit C is involved in oligogalacturonide (OG) internalization and OG-triggered immunity
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111274openalex-snapshot
Salicylic acid contributes to plant defense against a necrotroph: evidence from a transgenic NahG-expressing strain in Botrytis cinerea
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102651openalex-snapshot
Botrytis cinerea protease activity removes the chitin-binding domain of a major grapevine chitinase, abolishing its antifungal activity
inferred← citeshttps://doi.org/10.1016/j.tplants.2022.08.024openalex-snapshot
Killing softly: a roadmap of Botrytis cinerea pathogenicity
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c04908openalex-snapshot
Fungicidal Effect of Pyraclostrobin against Botrytis cinerea in Relation to Its Crystal Structure
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c03014openalex-snapshot
Novel Botrytis cinerea Zn(II) 2 Cys 6 Transcription Factor BcFtg1 Enhances the Virulence of the Gray Mold Fungus by Promoting Organic Acid Secretion and Carbon Source Utilization
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c02348openalex-snapshot
Enhancing Gene Knockout Efficiency in the Multinucleate Fungus Botrytis cinerea through High-Pressure Double Selection Combined with RNAi Triggering
inferred← citeshttps://doi.org/10.1038/s41467-021-22436-1openalex-snapshot
The Botrytis cinerea Crh1 transglycosylase is a cytoplasmic effector triggering plant cell death and defense response
inferred← citeshttps://doi.org/10.1038/s41467-023-41721-9openalex-snapshot
AlphaFold-Multimer predicts cross-kingdom interactions at the plant-pathogen interface
inferred← citeshttps://doi.org/10.1073/pnas.2422756122openalex-snapshot
Fungal Argonaute proteins act in bidirectional cross-kingdom RNA interference during plant infection
inferred← citeshttps://doi.org/10.1080/15427528.2022.2120145openalex-snapshot
Fungal diseases of eggplant (Solanum melongenaL.) and components of the disease triangle: A review
inferred← citeshttps://doi.org/10.1093/fqsafe/fyab016openalex-snapshot
Inhibition of Botrytis cinerea and control of gray mold on table grapes by calcium propionate
inferred← citeshttps://doi.org/10.1093/jxb/erae035openalex-snapshot
Contrasting cytosolic glutathione redox dynamics under abiotic and biotic stress in barley as revealed by the biosensor Grx1–roGFP2
inferred← citeshttps://doi.org/10.1093/plcell/koac040openalex-snapshot
Plant–microbe interactions in the apoplast: Communication at the plant cell wall
inferred← citeshttps://doi.org/10.1093/plphys/kiac476openalex-snapshot
Botrytis hypersensitive response inducing protein 1 triggers noncanonical PTI to induce plant cell death
inferred← citeshttps://doi.org/10.1101/2021.08.21.457223openalex-snapshot
Multiple knockout mutants reveal a high redundancy of phytotoxic compounds that determine necrotrophic pathogenesis of Botrytis cinerea
inferred← citeshttps://doi.org/10.1101/2023.09.29.560113openalex-snapshot
Networked proteins redundantly interact with VAP27 and RABG3 to regulate membrane tethering at the vacuole and beyond
inferred← citeshttps://doi.org/10.1101/2025.02.27.640524openalex-snapshot
The VelB intrinsically disordered domain promotes selective heterodimer formation of velvet domain regulatory proteins for fungal development
inferred← citeshttps://doi.org/10.1101/557983openalex-snapshot
Comparative proteomics of osmotic signal transduction mutants in Botrytis cinerea explain loss of pathogenicity phenotypes and highlight interaction with cAMP and Ca 2+ signalling pathways
inferred← citeshttps://doi.org/10.1104/pp.19.01052openalex-snapshot
The Chlamydomonas deg1c Mutant Accumulates Proteins Involved in High Light Acclimation
inferred← citeshttps://doi.org/10.1111/jam.15617openalex-snapshot
Degradation of oxalic acid by Trichoderma afroharzianum and its correlation with cell wall degrading enzymes in antagonizing Botrytis cinerea
inferred← citeshttps://doi.org/10.1111/mpp.13221openalex-snapshot
The evolutionary and molecular features of the broad‐host‐range plant pathogen Sclerotinia sclerotiorum
inferred← citeshttps://doi.org/10.1111/mpp.70004openalex-snapshot
Transcriptomic and functional analyses on a Botrytis cinerea multidrug‐resistant ( MDR ) strain provides new insights into the potential molecular mechanisms of MDR and fitness
inferred← citeshttps://doi.org/10.1111/nph.17104openalex-snapshot
Bitter and sweet make tomato hard to (b)eat
inferred← citeshttps://doi.org/10.1111/nph.20025openalex-snapshot
Plant infection by the necrotrophic fungus Botrytis requires actin‐dependent generation of high invasive turgor pressure
inferred← citeshttps://doi.org/10.1111/pbi.70689openalex-snapshot
Interactional Endocytosis and Transmembrane Transport Promote Cellular Internalization of Nano‐Delivered RNA Drugs for Efficient Control of Crop Diseases
inferred← citeshttps://doi.org/10.1111/pce.13732openalex-snapshot
VIPP2 interacts with VIPP1 and HSP22E/F at chloroplast membranes and modulates a retrograde signal for HSP22E/F gene expression
inferred← citeshttps://doi.org/10.1111/ppl.70156openalex-snapshot
Green light induces Solanum lycopersicum JA synthesis and inhibits Botrytis cinerea infection cushion formation to resist grey mould disease
inferred← citeshttps://doi.org/10.1111/tpj.14273openalex-snapshot
Hetero‐oligomeric CPN60 resembles highly symmetric group‐I chaperonin structure revealed by Cryo‐EM
inferred← citeshttps://doi.org/10.1128/aem.00819-24openalex-snapshot
Beyond morphogenesis and secondary metabolism: function of Velvet proteins and LaeA in fungal pathogenesis
inferred← citeshttps://doi.org/10.1128/mbio.00007-21openalex-snapshot
Compartmentalization of Melanin Biosynthetic Enzymes Contributes to Self-Defense against Intermediate Compound Scytalone in Botrytis cinerea
inferred← citeshttps://doi.org/10.1128/mbio.00133-24openalex-snapshot
The GATA transcription factor BcWCL2 regulates citric acid secretion to maintain redox homeostasis and full virulence in Botrytis cinerea
inferred← citeshttps://doi.org/10.1128/mmbr.00293-24openalex-snapshot
Velvet regulators as master integrators of development, metabolism, and pathogenicity in filamentous fungi
inferred← citeshttps://doi.org/10.1128/spectrum.00186-23openalex-snapshot
AfLaeA, a Global Regulator of Mycelial Growth, Chlamydospore Production, Pathogenicity, Secondary Metabolism, and Energy Metabolism in the Nematode-Trapping Fungus Arthrobotrys flagrans
inferred← citeshttps://doi.org/10.1146/annurev-arplant-061824-115733openalex-snapshot
Between Host and Invaders: The Subcellular Cell Wall Dynamics at the Plant–Pathogen Interface
inferred← citeshttps://doi.org/10.1186/s12866-024-03454-7openalex-snapshot
The Velvet transcription factor PnVeA regulates necrotrophic effectors and secondary metabolism in the wheat pathogen Parastagonospora nodorum
inferred← citeshttps://doi.org/10.1186/s12915-024-02043-4openalex-snapshot
Dual RNA-seq reveals distinct families of co-regulated and structurally conserved effectors in Botrytis cinerea infection of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1186/s13059-021-02446-4openalex-snapshot
Retrotransposons as pathogenicity factors of the plant pathogenic fungus Botrytis cinerea
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009434openalex-snapshot
The velvet protein Vel1 controls initial plant root colonization and conidia formation for xylem distribution in Verticillium wilt
inferred← citeshttps://doi.org/10.1371/journal.ppat.1007285openalex-snapshot
The MAPK kinase BcMkk1 suppresses oxalic acid biosynthesis via impeding phosphorylation of BcRim15 by BcSch9 in Botrytis cinerea
inferred← citeshttps://doi.org/10.1371/journal.ppat.1008326openalex-snapshot
CRISPR/Cas with ribonucleoprotein complexes and transiently selected telomere vectors allows highly efficient marker-free and multiple genome editing in Botrytis cinerea
inferred← citeshttps://doi.org/10.1371/journal.ppat.1010367openalex-snapshot
Multiple knockout mutants reveal a high redundancy of phytotoxic compounds contributing to necrotrophic pathogenesis of Botrytis cinerea
inferred← citeshttps://doi.org/10.1371/journal.ppat.1011885openalex-snapshot
A fungal RNA-dependent RNA polymerase is a novel player in plant infection and cross-kingdom RNA interference
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4183067/v1openalex-snapshot
Fungal Argonaute proteins act in bidirectional cross-kingdom RNA interference during plant infection
inferred← citeshttps://doi.org/10.2139/ssrn.5580664openalex-snapshot
Resistance of Botrytis cinerea to anilinopyrimidine fungicides: A novel ARMs-PCR method for the detection of Bcpos5 mutations and characterization of resistance using CRISPR/Cas9 editing
inferred← citeshttps://doi.org/10.26508/lsa.202503395openalex-snapshot
The VelB IDD promotes selective heterodimer formation of velvet proteins for fungal development
inferred← citeshttps://doi.org/10.3389/fmicb.2019.02829openalex-snapshot
A Similar Secretome Disturbance as a Hallmark of Non-pathogenic Botrytis cinerea ATMT-Mutants?
inferred← citeshttps://doi.org/10.3389/fmicb.2020.581203openalex-snapshot
LaeA Controls Virulence and Secondary Metabolism in Apple Canker Pathogen Valsa mali
inferred← citeshttps://doi.org/10.3389/fpls.2020.01286openalex-snapshot
Proteomic Studies to Understand the Mechanisms of Peach Tissue Degradation by Monilinia laxa
inferred← citeshttps://doi.org/10.3389/fpls.2020.591733openalex-snapshot
The Evolutionary and Molecular Features of Broad Host-Range Necrotrophy in Plant Pathogenic Fungi
inferred← citeshttps://doi.org/10.3389/fpls.2022.818483openalex-snapshot
A Secondary Metabolism Pathway Involved in the Production of a Putative Toxin Is Expressed at Early Stage of Monilinia laxa Infection
inferred← citeshttps://doi.org/10.3389/fpls.2023.1156804openalex-snapshot
Leaf resistance to Botrytis cinerea in wild tomato Solanum habrochaites depends on inoculum composition
inferred← citeshttps://doi.org/10.3390/agriculture14060932openalex-snapshot
Understanding the Biology of the Harmless Isolate Botrytis cinerea B459: An Approach to Bio-Targeted Toxin Identification
inferred← citeshttps://doi.org/10.3390/biology13121014openalex-snapshot
The Good, the Bad, and the Fungus: Insights into the Relationship Between Plants, Fungi, and Oomycetes in Hydroponics
inferred← citeshttps://doi.org/10.3390/foods14213666openalex-snapshot
Members of Velvet Complex FpVeA and FpVelB Regulate Asexual Development, Fumonisin Biosynthesis and Virulence in Fusarium proliferatum
inferred← citeshttps://doi.org/10.3390/jof10030216openalex-snapshot
Genome Comparisons between Botrytis fabae and the Closely Related Gray Mold Fungus Botrytis cinerea Reveal Possible Explanations for Their Contrasting Host Ranges
inferred← citeshttps://doi.org/10.3390/jof11080584openalex-snapshot
Proteomics-Based Approaches to Decipher the Molecular Strategies of Botrytis cinerea: A Review
inferred← citeshttps://doi.org/10.3390/jof11110786openalex-snapshot
The Velvet Complex Is Essential for Sclerotia Formation and Virulence in Sclerotinia sclerotiorum
inferred← citeshttps://doi.org/10.3390/jof7010032openalex-snapshot
Light-Photoreceptors and Proteins Related to Monilinia laxa Photoresponses
inferred← citeshttps://doi.org/10.3390/microorganisms14040829openalex-snapshot
Divergent Expression of Acidic and Alkaline Pectate Lyases in Ditylenchus destructor During Initial Infection Time Course
inferred← citeshttps://doi.org/10.3390/pathogens9110923openalex-snapshot
The Destructive Fungal Pathogen Botrytis cinerea—Insights from Genes Studied with Mutant Analysis
inferred← citeshttps://doi.org/10.3390/toxins17090433openalex-snapshot
Regulation of FpvelC on Conidiation, Pathogenicity and Secondary Metabolism in Fusarium proliferatum
inferred← citeshttps://doi.org/10.6084/m9.figshare.15179146openalex-snapshot
Additional file 1 of Retrotransposons as pathogenicity factors of the plant pathogenic fungus Botrytis cinerea
inferred← citeshttps://doi.org/10.6084/m9.figshare.15179152openalex-snapshot
Additional file 3 of Retrotransposons as pathogenicity factors of the plant pathogenic fungus Botrytis cinerea
inferred← citeshttps://doi.org/10.64898/2026.06.04.730115openalex-snapshot
Multi-knockout of 29 phytotoxic proteins and metabolites does not completely abolish virulence of the necrotrophic fungus Botrytis cinerea
inferred← citeshttps://doi.org/10.64898/2026.08.11.744170openalex-snapshot
Two homologous Alt a1-like fungal proteins possess dual activities in HIR-associated immune signaling and EDS1-dependent cell death
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