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Crop domestication and pathogen virulence: Interactions of tomato and Botrytis genetic diversity
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470380130.ch3openalex-snapshot
Enhancing Crop Gene Pools with Beneficial Traits Using Wild Relatives
inferredcites →https://doi.org/10.1006/pmpp.1998.0142openalex-snapshot
Detoxification of α-tomatine byBotrytis cinerea
inferredcites →https://doi.org/10.1007/978-0-585-34164-4_11openalex-snapshot
Integrated Control of Botrytis Cinerea on Greenhouse Tomatoes
inferredcites →https://doi.org/10.1007/978-1-4020-2626-3_1openalex-snapshot
Botrytis spp. and Diseases They Cause in Agricultural Systems – An Introduction
inferredcites →https://doi.org/10.1007/978-3-319-23371-0openalex-snapshot
Botrytis – the Fungus, the Pathogen and its Management in Agricultural Systems
inferredcites →https://doi.org/10.1007/978-3-319-23371-0_11openalex-snapshot
Control Strategies for Postharvest Grey Mould on Fruit Crops
inferredcites →https://doi.org/10.1007/bf00015609openalex-snapshot
The molecular biology of disease resistance
inferredcites →https://doi.org/10.1007/bf00226743openalex-snapshot
RFLP analysis of phylogenetic relationships and genetic variation in the genus Lycopersicon
inferredcites →https://doi.org/10.1007/bf02980727openalex-snapshot
Current status of vegetative compatibility groups in fusarium oxysporum
inferredcites →https://doi.org/10.1007/bf03356266openalex-snapshot
Fungicide resistance and genetic diversity of Botrytis cinerea isolates from a vineyard in Germany
inferredcites →https://doi.org/10.1007/s00122-006-0500-2openalex-snapshot
The construction of a Solanum habrochaites LYC4 introgression line population and the identification of QTLs for resistance to Botrytis cinerea
inferredcites →https://doi.org/10.1007/s00425-003-1143-zopenalex-snapshot
PCC1 : a merging point for pathogen defence and circadian signalling in Arabidopsis
inferredcites →https://doi.org/10.1007/s10658-006-9081-9openalex-snapshot
Partial stem and leaf resistance against the fungal pathogen Botrytis cinerea in wild relatives of tomato
inferredcites →https://doi.org/10.1007/s10681-007-9460-0openalex-snapshot
Quantitative resistance to Botrytis cinerea from Solanum neorickii
inferredcites →https://doi.org/10.1007/s11738-000-0046-xopenalex-snapshot
Screening of wild accessions resistant to gray mold (Botrytis cinerea Pers.) in Lycopersicon
inferredcites →https://doi.org/10.1007/s12154-014-0113-1openalex-snapshot
The rising threat of fungicide resistance in plant pathogenic fungi: Botrytis as a case study
inferredcites →https://doi.org/10.1016/j.biotechadv.2013.11.003openalex-snapshot
The history of tomato: From domestication to biopharming
inferredcites →https://doi.org/10.1016/j.cell.2006.12.006openalex-snapshot
The Molecular Genetics of Crop Domestication
inferredcites →https://doi.org/10.1016/j.micres.2011.10.006openalex-snapshot
Genetic diversity of a Botrytis cinerea cryptic species complex in Hungary
inferredcites →https://doi.org/10.1016/j.pbi.2004.05.002openalex-snapshot
Strategies used by bacterial pathogens to suppress plant defenses
inferredcites →https://doi.org/10.1016/j.pbi.2005.05.005openalex-snapshot
Suppression of host defense in compatible plant–Pseudomonas syringae interactions
inferredcites →https://doi.org/10.1016/j.pbi.2007.04.021openalex-snapshot
Microbe-associated molecular patterns (MAMPs) probe plant immunity
inferredcites →https://doi.org/10.1016/j.phytochem.2004.12.032openalex-snapshot
Metabolism and detoxification of phytoalexins and analogs by phytopathogenic fungi
inferredcites →https://doi.org/10.1016/j.phytochem.2010.11.018openalex-snapshot
Detoxification of cruciferous phytoalexins in Botrytis cinerea: Spontaneous dimerization of a camalexin metabolite
inferredcites →https://doi.org/10.1016/j.plantsci.2014.08.001openalex-snapshot
Tomato WRKY transcriptional factor SlDRW1 is required for disease resistance against Botrytis cinerea and tolerance to oxidative stress
inferredcites →https://doi.org/10.1016/j.tig.2006.09.011openalex-snapshot
Molecular evolution of plant immune system genes
inferredcites →https://doi.org/10.1016/j.tig.2012.10.011openalex-snapshot
Plant–pathogen interactions: disease resistance in modern agriculture
inferredcites →https://doi.org/10.1016/j.tplants.2008.10.006openalex-snapshot
Shades of gray: the world of quantitative disease resistance
inferredcites →https://doi.org/10.1016/j.tplants.2012.02.009openalex-snapshot
Unifying concepts and mechanisms in the specificity of plant–enemy interactions
inferredcites →https://doi.org/10.1016/s0031-9422(01)00088-7openalex-snapshot
Botrydial is produced in plant tissues infected by Botrytis cinerea
inferredcites →https://doi.org/10.1023/a:1008796006051openalex-snapshot
Evidence for Three Different Specific Saponin-detoxifying Activities in Botrytis cinerea and Cloning and Functional Analysis of a Gene Coding for a Putative Avenacinase
inferredcites →https://doi.org/10.1023/a:1015601731446openalex-snapshot
Durability of resistance against fungal, bacterial and viral pathogens; present situation
inferredcites →https://doi.org/10.1023/a:1018420504439openalex-snapshot
Effects of life history, domestication and agronomic selection on plant defence against insects: Evidence from maizes and wild relatives
inferredcites →https://doi.org/10.1023/a:1024222206991openalex-snapshot
Phenotypic Differences Between vacuma and transposa subpopulations of Botrytis cinerea
inferredcites →https://doi.org/10.1023/b:ejpp.0000010133.62052.e4openalex-snapshot
Resistance to Botrytis cinerea in Solanum lycopersicoides is Dominant in Hybrids with Tomato, and Involves induced Hyphal Death
inferredcites →https://doi.org/10.1038/35081161openalex-snapshot
Plant pathogens and integrated defence responses to infection
inferredcites →https://doi.org/10.1038/nature02485openalex-snapshot
Bacterial disease resistance in Arabidopsis through flagellin perception
inferredcites →https://doi.org/10.1038/ng.2704openalex-snapshot
The wheat powdery mildew genome shows the unique evolution of an obligate biotroph
inferredcites →https://doi.org/10.1038/ng.2747openalex-snapshot
Genomic analysis identifies targets of convergent positive selection in drug-resistant Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1038/ng.3447openalex-snapshot
Domestication selected for deceleration of the circadian clock in cultivated tomato
inferredcites →https://doi.org/10.1038/ng.3548openalex-snapshot
Genomic and functional analyses of Mycobacterium tuberculosis strains implicate ald in D-cycloserine resistance
inferredcites →https://doi.org/10.1038/nm934openalex-snapshot
Evidence for a tumoral immune resistance mechanism based on tryptophan degradation by indoleamine 2,3-dioxygenase
inferredcites →https://doi.org/10.1038/nrg.2016.132openalex-snapshot
Microbial genome-wide association studies: lessons from human GWAS
inferredcites →https://doi.org/10.1038/nrg2812openalex-snapshot
Plant immunity: towards an integrated view of plant–pathogen interactions
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01794.xopenalex-snapshot
Arabidopsis local resistance to Botrytis cinerea involves salicylic acid and camalexin and requires EDS4 and PAD2, but not SID2, EDS5 or PAD4
inferredcites →https://doi.org/10.1073/pnas.0604379103openalex-snapshot
Impacts of genetic bottlenecks on soybean genome diversity
inferredcites →https://doi.org/10.1073/pnas.102288999openalex-snapshot
Genetic variation for disease resistance and tolerance among Arabidopsis thaliana accessions
inferredcites →https://doi.org/10.1073/pnas.1306807110openalex-snapshot
Mosaic genome structure of the barley powdery mildew pathogen and conservation of transcriptional programs in divergent hosts
inferredcites →https://doi.org/10.1073/pnas.1309606110openalex-snapshot
Comparative transcriptomics reveals patterns of selection in domesticated and wild tomato
inferredcites →https://doi.org/10.1073/pnas.1508432112openalex-snapshot
A circadian oscillator in the fungus Botrytis cinerea regulates virulence when infecting Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/aob/mcm150openalex-snapshot
Domestication and Breeding of Tomatoes: What have We Gained and What Can We Gain in the Future?
inferredcites →https://doi.org/10.1093/bioinformatics/btq046openalex-snapshot
EBImage—an R package for image processing with applications to cellular phenotypes
inferredcites →https://doi.org/10.1093/genetics/142.1.285openalex-snapshot
Permutation Tests for Multiple Loci Affecting a Quantitative Character
inferredcites →https://doi.org/10.1094/mpmi-09-15-0196-ropenalex-snapshot
Expansive Phenotypic Landscape of Botrytis cinerea Shows Differential Contribution of Genetic Diversity and Plasticity
inferredcites →https://doi.org/10.1094/mpmi-09-15-0218-ropenalex-snapshot
Genome-Wide Association Study Identifies Novel Candidate Genes for Aggressiveness, Deoxynivalenol Production, and Azole Sensitivity in Natural Field Populations ofFusarium graminearum
inferredcites →https://doi.org/10.1094/mpmi-10-13-0313-iaopenalex-snapshot
Effectors as Tools in Disease Resistance Breeding Against Biotrophic, Hemibiotrophic, and Necrotrophic Plant Pathogens
inferredcites →https://doi.org/10.1094/mpmi-18-0602openalex-snapshot
Functional Analysis of the Cytochrome P450 Monooxygenase Gene bcbot1 of Botrytis cinerea Indicates That Botrydial Is a Strain-Specific Virulence Factor
inferredcites →https://doi.org/10.1094/mpmi-20-9-1126openalex-snapshot
Elevated Genetic Variation Within Virulence-AssociatedBotrytis cinereaPolygalacturonase Loci
inferredcites →https://doi.org/10.1094/mpmi-6-225openalex-snapshot
Gene-for-Genes Interactions Between CottonRGenes andXanthomonas campestrispv.malvacearum avrGenes
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/10.1094/mpmi.2003.16.4.360openalex-snapshot
Disruption of Botrytis cinerea Pectin Methylesterase Gene Bcpme1 Reduces Virulence on Several Host Plants
inferredcites →https://doi.org/10.1094/pd-89-1083openalex-snapshot
Genetic Structure of Botrytis cinerea Populations from Different Host Plants in California
inferredcites →https://doi.org/10.1094/pdis-01-12-0103-reopenalex-snapshot
Differences in Frequency of Transposable Elements Presence in Botrytis cinerea Populations from Several Hosts in Greece
inferredcites →https://doi.org/10.1094/phyto-02-16-0113-fiopenalex-snapshot
Validation of Genome-Wide Association Studies as a Tool to Identify Virulence Factors inParastagonospora nodorum
inferredcites →https://doi.org/10.1094/phyto.1999.89.10.967openalex-snapshot
Two Sibling Species of the Botrytis cinerea Complex, transposa and vacuma, Are Found in Sympatry on Numerous Host Plants
inferredcites →https://doi.org/10.1104/pp.001453openalex-snapshot
The Role of Ethylene and Wound Signaling in Resistance of Tomato to Botrytis cinerea
inferredcites →https://doi.org/10.1104/pp.105.068874openalex-snapshot
A Circadian Rhythm-Regulated Tomato Gene Is Induced by Arachidonic Acid and Phythophthora infestans Infection
inferredcites →https://doi.org/10.1104/pp.107.095596openalex-snapshot
Resistance to Botrytis cinerea Induced in Arabidopsis by Elicitors Is Independent of Salicylic Acid, Ethylene, or Jasmonate Signaling But Requires PHYTOALEXIN DEFICIENT3
inferredcites →https://doi.org/10.1105/tpc.018119openalex-snapshot
The Genetic, Developmental, and Molecular Bases of Fruit Size and Shape Variation in Tomato
inferredcites →https://doi.org/10.1105/tpc.108.059477openalex-snapshot
Tomato Protein Kinase 1b Mediates Signaling of Plant Responses to Necrotrophic Fungi and Insect Herbivory
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb00501.xopenalex-snapshot
VARIATION IN RESISTANCE AND VIRULENCE IN THE INTERACTION BETWEEN ARABIDOPSIS THALIANA AND A BACTERIAL PATHOGEN
inferredcites →https://doi.org/10.1111/j.0960-7412.2004.02059.xopenalex-snapshot
Identification of Botrytis cinerea susceptibility loci in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1095-8312.2011.01627.xopenalex-snapshot
The evolutionary improbability of ‘generalism’ in nature, with special reference to insects
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.1364-3703.2011.00783.xopenalex-snapshot
The Top 10 fungal pathogens in molecular plant pathology
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02508.xopenalex-snapshot
Secondary metabolites influence Arabidopsis/Botrytis interactions: variation in host production and pathogen sensitivity
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03794.xopenalex-snapshot
The ABC transporter BcatrB from Botrytis cinerea exports camalexin and is a virulence factor on Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02927.xopenalex-snapshot
Continua of specificity and virulence in plant host–pathogen interactions: causes and consequences
inferredcites →https://doi.org/10.1111/j.1574-6941.2010.00939.xopenalex-snapshot
A fungal pathogen in time and space: the population dynamics of Beauveria bassiana in a conifer forest
inferredcites →https://doi.org/10.1111/tpj.12964openalex-snapshot
An untargeted global metabolomic analysis reveals the biochemical changes underlying basal resistance and priming in Solanum lycopersicum, and identifies 1‐methyltryptophan as a metabolite involved in plant responses to Botrytis cinerea and Pseudomonas syringae
inferredcites →https://doi.org/10.1126/science.1171647openalex-snapshot
Innate Immunity in Plants: An Arms Race Between Pattern Recognition Receptors in Plants and Effectors in Microbial Pathogens
inferredcites →https://doi.org/10.1126/science.277.5329.1063openalex-snapshot
Seed Banks and Molecular Maps: Unlocking Genetic Potential from the Wild
inferredcites →https://doi.org/10.1128/ec.00164-12openalex-snapshot
Genome Update of Botrytis cinerea Strains B05.10 and T4
inferredcites →https://doi.org/10.1139/g01-124openalex-snapshot
A molecular linkage map of tomato displaying chromosomal locations of resistance gene analogs based on aLycopersicon esculentum×Lycopersicon hirsutumcross
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154055openalex-snapshot
Hormonal Modulation of Plant Immunity
inferredcites →https://doi.org/10.1146/annurev.phyto.010708.154114openalex-snapshot
The Origins of Plant Pathogens in Agro-Ecosystems
inferredcites →https://doi.org/10.1146/annurev.phyto.43.040204.135923openalex-snapshot
Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens
inferredcites →https://doi.org/10.1155/2013/572784openalex-snapshot
Plant Domestication and Resistance to Herbivory
inferredcites →https://doi.org/10.1186/1471-2105-14-45openalex-snapshot
Snpdat: Easy and rapid annotation of results from de novo snp discovery projects for model and non-model organisms
inferredcites →https://doi.org/10.1186/gb-2004-5-2-r12openalex-snapshot
Versatile and open software for comparing large genomes
inferredcites →https://doi.org/10.1371/journal.pgen.1005789openalex-snapshot
The Quantitative Basis of the Arabidopsis Innate Immune System to Endemic Pathogens Depends on Pathogen Genetics
inferredcites →https://doi.org/10.1371/journal.pone.0026968openalex-snapshot
Defence Responses of Arabidopsis thaliana to Infection by Pseudomonas syringae Are Regulated by the Circadian Clock
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.0053525openalex-snapshot
A Genome-Wide Association Study Identifies Genomic Regions for Virulence in the Non-Model Organism Heterobasidion annosum s.s
inferredcites →https://doi.org/10.1371/journal.pone.0078525openalex-snapshot
The High-Affinity Phosphodiesterase BcPde2 Has Impact on Growth, Differentiation and Virulence of the Phytopathogenic Ascomycete Botrytis cinerea
inferredcites →https://doi.org/10.1371/journal.pone.0126880openalex-snapshot
Accounting for Genetic Architecture Improves Sequence Based Genomic Prediction for a Drosophila Fitness Trait
inferredcites →https://doi.org/10.1534/genetics.105.041780openalex-snapshot
Origins of Host-Specific Populations of the Blast Pathogen Magnaporthe oryzae in Crop Domestication With Subsequent Expansion of Pandemic Clones on Rice and Weeds of Rice
inferredcites →https://doi.org/10.1534/genetics.108.091439openalex-snapshot
Complex Genetics Control Natural Variation inArabidopsis thalianaResistance toBotrytis cinerea
inferredcites →https://doi.org/10.1534/genetics.112.146720openalex-snapshot
A Novel Generalized Ridge Regression Method for Quantitative Genetics
inferredcites →https://doi.org/10.18637/jss.v067.i01openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.2174/138920210790217927openalex-snapshot
Genomics of Fungal Disease Resistance in Tomato
inferredcites →https://doi.org/10.22004/ag.econ.7670openalex-snapshot
Understanding Global Trends in the Use of Wheat Diversity and International Flows of Wheat Genetic Resources
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3389/fmicb.2015.00996openalex-snapshot
Whole genome resequencing of Botrytis cinerea isolates identifies high levels of standing diversity
inferredcites →https://doi.org/10.3389/fpls.2014.00435openalex-snapshot
Genome-wide transcriptional profiling of Botrytis cinerea genes targeting plant cell walls during infections of different hosts
inferredcites →https://doi.org/10.3389/fpls.2014.00450openalex-snapshot
Patterns of genomic variation in the poplar rust fungus Melampsora larici-populina identify pathogenesis-related factors
inferredcites →https://doi.org/10.3389/fpls.2014.00759openalex-snapshot
Comparative genomics of Australian isolates of the wheat stem rust pathogen Puccinia graminis f. sp. tritici reveals extensive polymorphism in candidate effector genes
inferredcites →https://doi.org/10.3389/fpls.2016.01010openalex-snapshot
Genome Wide Association Mapping in Arabidopsis thaliana Identifies Novel Genes Involved in Linking Allyl Glucosinolate to Altered Biomass and Defense
inferredcites →https://doi.org/10.3389/fpls.2017.00148openalex-snapshot
Comparative Genomics Integrated with Association Analysis Identifies Candidate Effector Genes Corresponding to Lr20 in Phenotype-Paired Puccinia triticina Isolates from Australia
inferredcites →https://doi.org/10.3389/fpls.2017.00763openalex-snapshot
Genome-Wide Association Studies In Plant Pathosystems: Toward an Ecological Genomics Approach
inferredcites →https://doi.org/10.3929/ethz-b-000105397openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.4049/jimmunol.181.8.5396openalex-snapshot
The Indoleamine 2,3-Dioxygenase Pathway Is Essential for Human Plasmacytoid Dendritic Cell-Induced Adaptive T Regulatory Cell Generation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Molecular Basis of Disease Resistance and Perspectives on Breeding Strategies for Resistance Improvement in Crops
inferred← citeshttps://doi.org/10.1016/j.sjbs.2023.103605openalex-snapshot
Functional annotation and comparative analysis of four Botrytis cinerea mitogenomes reported from Punjab, Pakistan
inferred← citeshttps://doi.org/10.1093/g3journal/jkab175openalex-snapshot
Quantitative interactions: the disease outcome of Botrytis cinerea across the plant kingdom
inferred← citeshttps://doi.org/10.1111/nph.15220openalex-snapshot
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Plant–necrotroph co-transcriptome networks illuminate a metabolic battlefield
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