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Characterization of the early response of Arabidopsis thaliana to Dickeya dadantii infection using expression profiling
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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/j.1460-2075.1990.tb08252.xopenalex-snapshot
Protease secretion by Erwinia chrysanthemi: the specific secretion functions are analogous to those of Escherichia coli alpha‐haemolysin.
inferredcites →https://doi.org/10.1002/pmic.200300814openalex-snapshot
The secretome of the plant pathogenic bacterium Erwinia chrysanthemi
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/bf01874480openalex-snapshot
Activation of defense-related genes in parsley leaves by infection withErwinia chrysanthemi
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Studies on the initiation of bacterial soft rot in potato tubers
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A conditionally fertile coi1 allele indicates cross-talk between plant hormone signalling pathways in Arabidopsis thaliana seeds and young seedlings
inferredcites →https://doi.org/10.1007/s00425-007-0627-7openalex-snapshot
Regulation of plant glucosinolate metabolism
inferredcites →https://doi.org/10.1007/s00425-008-0694-4openalex-snapshot
The role of JAR1 in Jasmonoyl-l-isoleucine production during Arabidopsis wound response
inferredcites →https://doi.org/10.1016/0031-9422(92)83609-3openalex-snapshot
Effects of wounding on glucosinolates in the cotyledons of oilseed rape and mustard
inferredcites →https://doi.org/10.1016/j.jplph.2005.11.011openalex-snapshot
Type III effector proteins from the plant pathogen Xanthomonas and their role in the interaction with the host plant
inferredcites →https://doi.org/10.1016/j.jplph.2011.01.018openalex-snapshot
Proteomic identification of differentially expressed proteins in Arabidopsis in response to methyl jasmonate
inferredcites →https://doi.org/10.1016/j.nbt.2015.11.001openalex-snapshot
Jasmonate signaling in plant stress responses and development – active and inactive compounds
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.phytochem.2006.09.004openalex-snapshot
Gene expression and glucosinolate accumulation in Arabidopsis thaliana in response to generalist and specialist herbivores of different feeding guilds and the role of defense signaling pathways
inferredcites →https://doi.org/10.1016/j.plantsci.2012.02.009openalex-snapshot
T3SS-dependent differential modulations of the jasmonic acid pathway in susceptible and resistant genotypes of Malus spp. challenged with Erwinia amylovora
inferredcites →https://doi.org/10.1016/s1360-1385(98)01199-6openalex-snapshot
Pathogen defence in plants — a paradigm of biological complexity
inferredcites →https://doi.org/10.1016/s1369-5274(99)00054-5openalex-snapshot
Effector proteins of phytopathogenic bacteria: bifunctional signals in virulence and host recognition
inferredcites →https://doi.org/10.1038/82521openalex-snapshot
The transcriptome of Arabidopsis thaliana during systemic acquired resistance
inferredcites →https://doi.org/10.1038/nchembio.164openalex-snapshot
Networking by small-molecule hormones in plant immunity
inferredcites →https://doi.org/10.1046/j.0032-0862.2001.shortopenalex-snapshot
Potato diseases caused by soft rot erwinias: an overview of pathogenesis
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00265.xopenalex-snapshot
Plants have a sensitive perception system for the most conserved domain of bacterial flagellin
inferredcites →https://doi.org/10.1073/pnas.040569997openalex-snapshot
Arabidopsis cytochrome P450s that catalyze the first step of tryptophan-dependent indole-3-acetic acid biosynthesis
inferredcites →https://doi.org/10.1073/pnas.190264497openalex-snapshot
The Arabidopsis male-sterile mutant, opr3 , lacks the 12-oxophytodienoic acid reductase required for jasmonate synthesis
inferredcites →https://doi.org/10.1073/pnas.89.15.6837openalex-snapshot
Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant.
inferredcites →https://doi.org/10.1074/jbc.m407681200openalex-snapshot
Desulfoglucosinolate Sulfotransferases from Arabidopsis thaliana Catalyze the Final Step in the Biosynthesis of the Glucosinolate Core Structure
inferredcites →https://doi.org/10.1093/jxb/ers389openalex-snapshot
TGA transcription factors and jasmonate-independent COI1 signalling regulate specific plant responses to reactive oxylipins
inferredcites →https://doi.org/10.1093/mp/ssn013openalex-snapshot
Kunitz Trypsin Inhibitor: An Antagonist of Cell Death Triggered by Phytopathogens and Fumonisin B1 in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gkg071openalex-snapshot
CATMA: a complete Arabidopsis GST database
inferredcites →https://doi.org/10.1093/nar/gkh894openalex-snapshot
The FunCat, a functional annotation scheme for systematic classification of proteins from whole genomes
inferredcites →https://doi.org/10.1093/nar/gkm757openalex-snapshot
CATdb: a public access to Arabidopsis transcriptome data from the URGV-CATMA platform
inferredcites →https://doi.org/10.1094/mpmi-20-7-0794openalex-snapshot
Arabidopsis thaliana Expresses Multiple Lines of Defense to Counterattack Erwinia chrysanthemi
inferredcites →https://doi.org/10.1094/mpmi-6-197openalex-snapshot
Pathogenic Behavior of Pectinase-DefectiveErwinia chrysanthemiMutants on Different Plants
inferredcites →https://doi.org/10.1094/mpmi-7-0356openalex-snapshot
Salicylic Acid Induced Resistance toErwinia carotovorasubsp,carotovorain Tobacco
inferredcites →https://doi.org/10.1094/mpmi-7-0573openalex-snapshot
Erwinia chrysanthemi hrpGenesand Their Involvement in Soft Rot Pathogenesisand Elicitation of the Hypersensitive Response
inferredcites →https://doi.org/10.1094/mpmi-8-0484openalex-snapshot
Erwiniachrysanthemi HarpinEch: An Elicitorof the Hypersensitive Response that Contributesto Soft-Rot Pathogenesis
inferredcites →https://doi.org/10.1094/mpmi.2002.15.5.472openalex-snapshot
hrp Genes of Erwinia chrysanthemi 3937 Are Important Virulence Factors
inferredcites →https://doi.org/10.1094/mpmi.2003.16.3.179openalex-snapshot
Erwinia carotovora subsp. carotovora and Erwinia-Derived Elicitors HrpN and PehA Trigger Distinct but Interacting Defense Responses and Cell Death in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.1035402openalex-snapshot
Trp-dependent auxin biosynthesis in Arabidopsis: involvement of cytochrome P450s CYP79B2 and CYP79B3
inferredcites →https://doi.org/10.1101/gr.2544504openalex-snapshot
Versatile Gene-Specific Sequence Tags forArabidopsisFunctional Genomics: Transcript Profiling and Reverse Genetics Applications
inferredcites →https://doi.org/10.1104/pp.011015openalex-snapshot
Modulation of CYP79 Genes and Glucosinolate Profiles in Arabidopsis by Defense Signaling Pathways
inferredcites →https://doi.org/10.1104/pp.104.053389openalex-snapshot
Major Signaling Pathways Modulate Arabidopsis Glucosinolate Accumulation and Response to Both Phloem-Feeding and Chewing Insects
inferredcites →https://doi.org/10.1104/pp.104.054395openalex-snapshot
The Arabidopsis ATR1 Myb Transcription Factor Controls Indolic Glucosinolate Homeostasis
inferredcites →https://doi.org/10.1104/pp.105.067058openalex-snapshot
12-Oxo-Phytodienoic Acid Triggers Expression of a Distinct Set of Genes and Plays a Role in Wound-Induced Gene Expression in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.119321openalex-snapshot
Induction of the Arabidopsis PHO1;H10 Gene by 12-Oxo-Phytodienoic Acid But Not Jasmonic Acid via a CORONATINE INSENSITIVE1-Dependent Pathway
inferredcites →https://doi.org/10.1104/pp.125.4.1688openalex-snapshot
Study of the Role of Antimicrobial Glucosinolate-Derived Isothiocyanates in Resistance of Arabidopsis to Microbial Pathogens
inferredcites →https://doi.org/10.1104/pp.126.2.849openalex-snapshot
Jasmonate-Dependent Induction of Indole Glucosinolates in Arabidopsis by Culture Filtrates of the Nonspecific PathogenErwinia carotovora
inferredcites →https://doi.org/10.1105/tpc.000885openalex-snapshot
Jasmonate Response Locus JAR1 and Several Related Arabidopsis Genes Encode Enzymes of the Firefly Luciferase Superfamily That Show Activity on Jasmonic, Salicylic, and Indole-3-Acetic Acids in an Assay for Adenylation
inferredcites →https://doi.org/10.1105/tpc.007591openalex-snapshot
Quantitative Nature of Arabidopsis Responses during Compatible and Incompatible Interactions with the Bacterial PathogenPseudomonas syringae [W]
inferredcites →https://doi.org/10.1105/tpc.016980openalex-snapshot
The WRKY70 Transcription Factor: A Node of Convergence for Jasmonate-Mediated and Salicylate-Mediated Signals in Plant Defense[W]
inferredcites →https://doi.org/10.1105/tpc.104.022236openalex-snapshot
Genome-Wide Analysis of Arabidopsis Pentatricopeptide Repeat Proteins Reveals Their Essential Role in Organelle Biogenesis[W]
inferredcites →https://doi.org/10.1105/tpc.109.065730openalex-snapshot
The Arabidopsis CORONATINE INSENSITIVE1 Protein Is a Jasmonate Receptor
inferredcites →https://doi.org/10.1111/1758-2229.12166openalex-snapshot
Bacterial pectate lyases, structural and functional diversity
inferredcites →https://doi.org/10.1111/j.1364-3703.2007.00437.xopenalex-snapshot
Abscisic acid deficiency leads to rapid activation of tomato defence responses upon infection with Erwinia chrysanthemi
inferredcites →https://doi.org/10.1111/j.1365-2672.2009.04181.xopenalex-snapshot
Initialin vitroevaluations of the antibacterial activities of glucosinolate enzymatic hydrolysis products against plant pathogenic bacteria
inferredcites →https://doi.org/10.1111/j.1365-2958.1992.tb01775.xopenalex-snapshot
Some of the out genes involved in the secretion of pectate lyases in Erwinia chrysanthemi are regulated by kdgR
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06888.xopenalex-snapshot
Bacterial chemoattraction towards jasmonate plays a role in the entry of Dickeya dadantii through wounded tissues
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07388.xopenalex-snapshot
Systematic targeted mutagenesis of the MarR/SlyA family members of Dickeya dadantii 3937 reveals a role for MfbR in the modulation of virulence gene expression in response to acidic pH
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02451.xopenalex-snapshot
Siderophore‐mediated upregulation of Arabidopsis ferritin expression in response to Erwinia chrysanthemi infection
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02560.xopenalex-snapshot
Coordinated activation of metabolic pathways for antioxidants and defence compounds by jasmonates and their roles in stress tolerance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02725.xopenalex-snapshot
Genome‐wide transcriptional analysis of the Arabidopsis thaliana interaction with the plant pathogen Pseudomonas syringae pv. tomato DC3000 and the human pathogen Escherichia coli O157:H7
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03099.xopenalex-snapshot
The transcription factor HIG1/MYB51 regulates indolic glucosinolate biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03775.xopenalex-snapshot
NRAMP genes function in Arabidopsis thaliana resistance to Erwinia chrysanthemi infection
inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01473.xopenalex-snapshot
The GacA global regulator is required for the appropriate expression of Erwinia chrysanthemi 3937 pathogenicity genes during plant infection
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/mpp.12345openalex-snapshot
Gram‐negative phytopathogenic bacteria, all hemibiotrophs after all?
inferredcites →https://doi.org/10.1111/mpp.12549openalex-snapshot
Transcriptome analysis of the Dickeya dadantii PecS regulon during the early stages of interaction with Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1163732openalex-snapshot
A Glucosinolate Metabolism Pathway in Living Plant Cells Mediates Broad-Spectrum Antifungal Defense
inferredcites →https://doi.org/10.1126/science.1164627openalex-snapshot
Glucosinolate Metabolites Required for an Arabidopsis Innate Immune Response
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105449openalex-snapshot
Growth Control and Cell Wall Signaling in Plants
inferredcites →https://doi.org/10.1146/annurev-phyto-081211-173013openalex-snapshot
The Role of Secretion Systems and Small Molecules in Soft-Rot Enterobacteriaceae Pathogenicity
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105228openalex-snapshot
BIOLOGY AND BIOCHEMISTRY OF GLUCOSINOLATES
inferredcites →https://doi.org/10.1146/annurev.micro.50.1.213openalex-snapshot
REGULATION OF PECTINOLYSIS IN ERWINIA CHRYSANTHEMI
inferredcites →https://doi.org/10.1146/annurev.phyto.37.1.307openalex-snapshot
W ITHHOLDING AND E XCHANGING I RON : Interactions Between Erwinia spp. and Their Plant Hosts
inferredcites →https://doi.org/10.1146/annurev.py.18.090180.002045openalex-snapshot
Ecology of the Soft Rot Erwinias
inferredcites →https://doi.org/10.1146/annurev.py.24.090186.002123openalex-snapshot
The Role of Pectic Enzymes in Plant Pathogenesis
inferredcites →https://doi.org/10.1146/annurev.py.32.090194.001221openalex-snapshot
EXTRACELLULAR ENZYMES AND PATHOGENESIS OF SOFT-ROT ERWINIA
inferredcites →https://doi.org/10.1199/tab.0134openalex-snapshot
Glucosinolate Breakdown in Arabidopsis: Mechanism, Regulation and Biological Significance
inferredcites →https://doi.org/10.1371/journal.pone.0018991openalex-snapshot
Analysis of the Plant bos1 Mutant Highlights Necrosis as an Efficient Defence Mechanism during D. dadantii/Arabidospis thaliana Interaction
inferredcites →https://doi.org/10.1371/journal.pone.0113718openalex-snapshot
Transcriptome Analysis Reveals Genes Commonly Induced by Botrytis cinerea Infection, Cold, Drought and Oxidative Stresses in Arabidopsis
inferredcites →https://doi.org/10.3102/10769986025001060openalex-snapshot
On the Adaptive Control of the False Discovery Rate in Multiple Testing With Independent Statistics
inferredcites →https://doi.org/10.3389/fpls.2017.00456openalex-snapshot
Manipulation of ABA Content in Arabidopsis thaliana Modifies Sensitivity and Oxidative Stress Response to Dickeya dadantii and Influences Peroxidase Activity
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-030-61459-1_4openalex-snapshot
Molecular Interactions of Pectobacterium and Dickeya with Plants
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