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The Function of Glucosinolates and Related Metabolites in Plant Innate Immunity
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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/bies.201400124openalex-snapshot
Defensive weapons and defense signals in plants: Some metabolites serve both roles
inferredcites →https://doi.org/10.1002/cbic.201200086openalex-snapshot
Sulfur‐Containing Secondary Metabolites from Arabidopsis thaliana and other Brassicaceae with Function in Plant Immunity
inferredcites →https://doi.org/10.1007/978-1-4899-2635-7openalex-snapshot
The Fungal Spore and Disease Initiation in Plants and Animals
inferredcites →https://doi.org/10.1007/978-1-4899-2635-7_15openalex-snapshot
Invasion of Plants by Powdery Mildew Fungi, and Cellular Mechanisms of Resistance
inferredcites →https://doi.org/10.1016/j.cell.2006.02.008openalex-snapshot
Host-Microbe Interactions: Shaping the Evolution of the Plant Immune Response
inferredcites →https://doi.org/10.1016/j.cell.2006.06.054openalex-snapshot
Plant Stomata Function in Innate Immunity against Bacterial Invasion
inferredcites →https://doi.org/10.1016/j.cell.2016.02.028openalex-snapshot
Root Endophyte Colletotrichum tofieldiae Confers Plant Fitness Benefits that Are Phosphate Status Dependent
inferredcites →https://doi.org/10.1016/j.copbio.2010.05.006openalex-snapshot
Plant stomata: a checkpoint of host immunity and pathogen virulence
inferredcites →https://doi.org/10.1016/j.jplph.2010.06.014openalex-snapshot
When and how to kill a plant cell: Infection strategies of plant pathogenic fungi
inferredcites →https://doi.org/10.1016/j.mib.2008.12.003openalex-snapshot
Pseudomonas syringae type III secretion system effectors: repertoires in search of functions
inferredcites →https://doi.org/10.1016/j.molp.2016.01.005openalex-snapshot
Regulatory and Functional Aspects of Indolic Metabolism in Plant Systemic Acquired Resistance
inferredcites →https://doi.org/10.1016/j.molp.2016.01.006openalex-snapshot
Regulation of Pathogen-Triggered Tryptophan Metabolism in Arabidopsis thaliana by MYB Transcription Factors and Indole Glucosinolate Conversion Products
inferredcites →https://doi.org/10.1016/j.pbi.2011.08.002openalex-snapshot
Cell biology of the plant–powdery mildew interaction
inferredcites →https://doi.org/10.1016/j.pbi.2012.03.002openalex-snapshot
Chemical warfare or modulators of defence responses – the function of secondary metabolites in plant immunity
inferredcites →https://doi.org/10.1016/j.phytochem.2006.02.024openalex-snapshot
The enzymic and chemically induced decomposition of glucosinolates
inferredcites →https://doi.org/10.1016/j.phytochem.2008.03.006openalex-snapshot
β-Glucosidases as detonators of plant chemical defense
inferredcites →https://doi.org/10.1016/j.phytochem.2014.07.024openalex-snapshot
Non-indolyl cruciferous phytoalexins: Nasturlexins and tridentatols, a striking convergent evolution of defenses in terrestrial plants and marine animals?
inferredcites →https://doi.org/10.1016/j.phytochem.2015.08.009openalex-snapshot
Expanding the nasturlexin family: Nasturlexins C and D and their sulfoxides are phytoalexins of the crucifers Barbarea vulgaris and B. verna
inferredcites →https://doi.org/10.1016/j.tplants.2011.11.002openalex-snapshot
Phytoalexins in defense against pathogens
inferredcites →https://doi.org/10.1021/ja00094a021openalex-snapshot
Biosynthesis of Cruciferous Phytoalexins
inferredcites →https://doi.org/10.1023/a:1026592509060openalex-snapshot
Hypersensitive response-related death
inferredcites →https://doi.org/10.1038/cdd.2011.37openalex-snapshot
Programmed cell death in the plant immune system
inferredcites →https://doi.org/10.1038/nature14907openalex-snapshot
A new cyanogenic metabolite in Arabidopsis required for inducible pathogen defence
inferredcites →https://doi.org/10.1038/nrg2812openalex-snapshot
Plant immunity: towards an integrated view of plant–pathogen interactions
inferredcites →https://doi.org/10.1038/srep00171openalex-snapshot
Non-host resistance to penetration and hyphal growth of Magnaporthe oryzae in Arabidopsis
inferredcites →https://doi.org/10.1039/c0ob00265hopenalex-snapshot
Unveiling the phytoalexin biosynthetic puzzle in salt cress: unprecedented incorporation of glucobrassicin into wasalexins A and B
inferredcites →https://doi.org/10.1039/c1np00020aopenalex-snapshot
The phytoalexins from cultivated and wild crucifers: Chemistry and biology
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00513.xopenalex-snapshot
Deficiency in phytoalexin production causes enhanced susceptibility of Arabidopsis thaliana to the fungus Alternaria brassicicola
inferredcites →https://doi.org/10.1073/pnas.0305876101openalex-snapshot
Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1218701110openalex-snapshot
Perception of conserved pathogen elicitors at the plasma membrane leads to relocalization of the Arabidopsis PEN3 transporter
inferredcites →https://doi.org/10.1073/pnas.1305745110openalex-snapshot
Glutathione and tryptophan metabolism are required for Arabidopsis immunity during the hypersensitive response to hemibiotrophs
inferredcites →https://doi.org/10.1073/pnas.98.2.753openalex-snapshot
Accumulation of soluble and wall-bound indolic metabolites in Arabidopsis thaliana leaves infected with virulent or avirulent Pseudomonas syringae pathovar tomato strains
inferredcites →https://doi.org/10.1093/aob/mcu120openalex-snapshot
Callose biosynthesis in arabidopsis with a focus on pathogen response: what we have learned within the last decade
inferredcites →https://doi.org/10.1093/mp/ssn014openalex-snapshot
Mutation of a Gene in the Fungus Leptosphaeria maculans Allows Increased Frequency of Penetration of Stomatal Apertures of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/mp/sss044openalex-snapshot
Transcriptional Activation and Production of Tryptophan-Derived Secondary Metabolites in Arabidopsis Roots Contributes to the Defense against the Fungal Vascular Pathogen Verticillium longisporum
inferredcites →https://doi.org/10.1093/pcp/pcp066openalex-snapshot
Myrosinases, TGG1 and TGG2, Redundantly Function in ABA and MeJA Signaling in Arabidopsis Guard Cells
inferredcites →https://doi.org/10.1094/mpmi-03-12-0071-ropenalex-snapshot
Indole-3-Acetaldoxime-Derived Compounds Restrict Root Colonization in the Beneficial Interaction Between Arabidopsis Roots and the Endophyte Piriformospora indica
inferredcites →https://doi.org/10.1094/mpmi-07-10-0149openalex-snapshot
Callose Deposition: A Multifaceted Plant Defense Response
inferredcites →https://doi.org/10.1094/mpmi-21-11-1421openalex-snapshot
Characterization of Nonhost Resistance of Arabidopsis to the Asian Soybean Rust
inferredcites →https://doi.org/10.1094/mpmi-22-11-1331openalex-snapshot
AGB1 and PMR5 Contribute to PEN2-Mediated Preinvasion Resistance to Magnaporthe oryzae in Arabidopsis thaliana
inferredcites →https://doi.org/10.1094/phyto-08-12-0201-ropenalex-snapshot
Nonhost Resistance of Arabidopsis thaliana Against Alternaria alternata Involves both Pre- and Postinvasive Defenses but Is Collapsed by AAL-Toxin in the Absence of LOH2
inferredcites →https://doi.org/10.1099/mic.0.082362-0openalex-snapshot
The antibacterial properties of isothiocyanates
inferredcites →https://doi.org/10.1104/pp.010416openalex-snapshot
A Gene Controlling Variation in Arabidopsis Glucosinolate Composition Is Part of the Methionine Chain Elongation Pathway
inferredcites →https://doi.org/10.1104/pp.104.057794openalex-snapshot
Structural Complexity, Differential Response to Infection, and Tissue Specificity of Indolic and Phenylpropanoid Secondary Metabolism in Arabidopsis Roots
inferredcites →https://doi.org/10.1104/pp.111.176446openalex-snapshot
Broad-Spectrum Suppression of Innate Immunity Is Required for Colonization of Arabidopsis Roots by the Fungus Piriformospora indica
inferredcites →https://doi.org/10.1104/pp.114.235630openalex-snapshot
The Biosynthetic Pathway of Indole-3-Carbaldehyde and Indole-3-Carboxylic Acid Derivatives in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.251892openalex-snapshot
Involvement of the Electrophilic Isothiocyanate Sulforaphane in Arabidopsis Local Defense Responses
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.15.00182openalex-snapshot
Mutant Allele-Specific Uncoupling of PENETRATION3 Functions Reveals Engagement of the ATP-Binding Cassette Transporter in Distinct Tryptophan Metabolic Pathways
inferredcites →https://doi.org/10.1104/pp.97.1.217openalex-snapshot
Biochemical Genetics of Plant Secondary Metabolites in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.105.038372openalex-snapshot
ArabidopsisPEN3/PDR8, an ATP Binding Cassette Transporter, Contributes to Nonhost Resistance to Inappropriate Pathogens That Enter by Direct Penetration
inferredcites →https://doi.org/10.1105/tpc.107.051383openalex-snapshot
ArabidopsisCytochrome P450 Monooxygenase 71A13 Catalyzes the Conversion of Indole-3-Acetaldoxime in Camalexin Synthesis
inferredcites →https://doi.org/10.1105/tpc.108.063115openalex-snapshot
The Gene Controlling theIndole Glucosinolate Modifier1Quantitative Trait Locus Alters Indole Glucosinolate Structures and Aphid Resistance inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.063263openalex-snapshot
Functional Proteomics of Arabidopsis thaliana Guard Cells Uncovers New Stomatal Signaling Pathways
inferredcites →https://doi.org/10.1105/tpc.109.066670openalex-snapshot
The Multifunctional Enzyme CYP71B15 (PHYTOALEXIN DEFICIENT3) Converts Cysteine-Indole-3-Acetonitrile to Camalexin in the Indole-3-Acetonitrile Metabolic Network of Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.109.069658openalex-snapshot
Innate Immune Responses Activated in Arabidopsis Roots by Microbe-Associated Molecular Patterns
inferredcites →https://doi.org/10.1105/tpc.11.12.2419openalex-snapshot
Arabidopsis PAD3 , a Gene Required for Camalexin Biosynthesis, Encodes a Putative Cytochrome P450 Monooxygenase
inferredcites →https://doi.org/10.1105/tpc.110.074344openalex-snapshot
Entry Mode–Dependent Function of an Indole Glucosinolate Pathway in Arabidopsis for Nonhost Resistance against Anthracnose Pathogens
inferredcites →https://doi.org/10.1105/tpc.110.081711openalex-snapshot
Metabolic Engineering in Nicotiana benthamiana Reveals Key Enzyme Functions in Arabidopsis Indole Glucosinolate Modification
inferredcites →https://doi.org/10.1105/tpc.114.129726openalex-snapshot
Myrosin Idioblast Cell Fate and Development Are Regulated by theArabidopsisTranscription Factor FAMA, the Auxin Pathway, and Vesicular Trafficking
inferredcites →https://doi.org/10.1105/tpc.114.129874openalex-snapshot
FAMA Is an Essential Component for the Differentiation of Two Distinct Cell Types, Myrosin Cells and Guard Cells, in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00871openalex-snapshot
Pathogen-Responsive MPK3 and MPK6 Reprogram the Biosynthesis of Indole Glucosinolates and Their Derivatives in Arabidopsis Immunity
inferredcites →https://doi.org/10.1105/tpc.15.00887openalex-snapshot
Immobilized Subpopulations of Leaf Epidermal Mitochondria Mediate PENETRATION2-Dependent Pathogen Entry Control in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.6.9.1191openalex-snapshot
Two Classes of Plant Antibiotics: Phytoalexins versus "Phytoanticipins"
inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02385.xopenalex-snapshot
Allyl isothiocyanate (AITC) induces stomatal closure in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3059.2006.01497.xopenalex-snapshot
In vitro antifungal activity of brassinin, camalexin and two isothiocyanates against the crucifer pathogens Alternaria brassicicola and Alternaria brassicae
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.2006.02716.xopenalex-snapshot
Arabidopsis myrosinases TGG1 and TGG2 have redundant function in glucosinolate breakdown and insect defense
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02938.xopenalex-snapshot
Identification of PAD2 as a γ‐glutamylcysteine synthetase highlights the importance of glutathione in disease resistance of Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03424.xopenalex-snapshot
PYK10, a β‐glucosidase located in the endoplasmatic reticulum, is crucial for the beneficial interaction between Arabidopsis thaliana and the endophytic fungus Piriformospora indica
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04197.xopenalex-snapshot
Disease resistance of Arabidopsis to Phytophthora brassicae is established by the sequential action of indole glucosinolates and camalexin
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04224.xopenalex-snapshot
Tryptophan-derived secondary metabolites in Arabidopsis thaliana confer non-host resistance to necrotrophic Plectosphaerella cucumerina fungi
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04578.xopenalex-snapshot
Role of camalexin, indole glucosinolates, and side chain modification of glucosinolate‐derived isothiocyanates in defense of Arabidopsis against Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1111/j.1439-0434.1981.tb03327.xopenalex-snapshot
Phytoalexins — A Working Redefinition
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03824.xopenalex-snapshot
Conservation and clade-specific diversification of pathogen-inducible tryptophan and indole glucosinolate metabolism in Arabidopsis thaliana relatives
inferredcites →https://doi.org/10.1111/nph.12155openalex-snapshot
UDP ‐glucosyltransferase UGT 84A2/ BRT 1 is required for Arabidopsis nonhost resistance to the Asian soybean rust pathogen Phakopsora pachyrhizi
inferredcites →https://doi.org/10.1111/nph.13325openalex-snapshot
Secondary metabolites in plant innate immunity: conserved function of divergent chemicals
inferredcites →https://doi.org/10.1111/nph.13411openalex-snapshot
Mutualistic root endophytism is not associated with the reduction of saprotrophic traits and requires a noncompromised plant innate immunity
inferredcites →https://doi.org/10.1111/pce.12052openalex-snapshot
A novel A rabidopsis–oomycete pathosystem: differential interactions with P hytophthora capsici reveal a role for camalexin, indole glucosinolates and salicylic acid in defence
inferredcites →https://doi.org/10.1111/tpj.12571openalex-snapshot
Role of the penetration‐resistance genes PEN 1, PEN 2 and PEN 3 in the hypersensitive response and race‐specific resistance in A rabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1086716openalex-snapshot
Loss of a Callose Synthase Results in Salicylic Acid-Dependent Disease Resistance
inferredcites →https://doi.org/10.1126/science.1119409openalex-snapshot
Pre- and Postinvasion Defenses Both Contribute to Nonhost Resistance in Arabidopsis
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/10.1126/science.1199707openalex-snapshot
Pseudomonas sax Genes Overcome Aliphatic Isothiocyanate–Mediated Non-Host Resistance in Arabidopsis
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105228openalex-snapshot
BIOLOGY AND BIOCHEMISTRY OF GLUCOSINOLATES
inferredcites →https://doi.org/10.1271/bbb.120928openalex-snapshot
Glucosinolate Degradation Products, Isothiocyanates, Nitriles, and Thiocyanates, Induce Stomatal Closure Accompanied by Peroxidase-Mediated Reactive Oxygen Species Production inArabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0001322openalex-snapshot
A Systems Biology Approach Identifies a R2R3 MYB Gene Subfamily with Distinct and Overlapping Functions in Regulation of Aliphatic Glucosinolates
inferredcites →https://doi.org/10.1371/journal.pone.0070771openalex-snapshot
The Effects of Glucosinolates and Their Breakdown Products on Necrotrophic Fungi
inferredcites →https://doi.org/10.3389/fpls.2013.00472openalex-snapshot
Regulation of reactive oxygen species-mediated abscisic acid signaling in guard cells and drought tolerance by glutathione
inferredcites →https://doi.org/10.3389/fpls.2015.00014openalex-snapshot
Perception of Arabidopsis AtPep peptides, but not bacterial elicitors, accelerates starvation-induced senescence
inferredcites →https://doi.org/10.3389/fpls.2015.00414openalex-snapshot
Glucosinolate-derived isothiocyanates impact mitochondrial function in fungal cells and elicit an oxidative stress response necessary for growth recovery
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112668zenodo-depositor-declared
Comparison of glucosinolate diversity in the crucifer tribe Cardamineae and the remaining order Brassicales highlights repetitive evolutionary loss and gain of biosynthetic steps
inferred← citeshttps://doi.org/10.1002/cjoc.202100353openalex-snapshot
Lepithiohydimerins A—D: Four Pairs of Neuroprotective Thiohydantoin Dimers Bearing a Disulfide Bond from Maca (Lepidium meyenii Walp.)
inferred← citeshttps://doi.org/10.1002/pld3.437openalex-snapshot
The isothiocyanate sulforaphane induces respiratory burst oxidase homologue D‐dependent reactive oxygen species production and regulates expression of stress response genes
inferred← citeshttps://doi.org/10.1007/978-981-16-1974-8_5openalex-snapshot
Biometabolomics of Host Resistance to Hemi-biotrophs and Necrotrophs
inferred← citeshttps://doi.org/10.1007/s11103-021-01181-5openalex-snapshot
The phosphorylated pathway of serine biosynthesis is crucial for indolic glucosinolate biosynthesis and plant growth promotion conferred by the root endophyte Colletotrichum tofieldiae
inferred← citeshttps://doi.org/10.1016/bs.abr.2021.01.008openalex-snapshot
Glucosinolates revisited—A follow-up of ABR volume 80: Glucosinolates
inferred← citeshttps://doi.org/10.1016/j.crvi.2019.03.005openalex-snapshot
Biosynthèse des glucosinolates indoliques et rôle écologique de leurs modifications secondaires
inferred← citeshttps://doi.org/10.1016/j.genrep.2021.101040openalex-snapshot
Secondary metabolites in the drought stress tolerance of crop plants: A review
inferred← citeshttps://doi.org/10.1016/j.isci.2022.105484openalex-snapshot
Integration of Transcriptome and Metabolome Analyses Reveals the Mechanistic Basis for Cadmium Accumulation in Maize
inferred← citeshttps://doi.org/10.1016/j.molp.2022.12.006openalex-snapshot
Specialized metabolites as versatile tools in shaping plant–microbe associations
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.05.006openalex-snapshot
Glucosinolate turnover in Brassicales species to an oxazolidin-2-one, formed via the 2-thione and without formation of thioamide
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112100openalex-snapshot
Glucosinolate structural diversity, identification, chemical synthesis and metabolism in plants
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112571openalex-snapshot
Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113742openalex-snapshot
Phytoalexins of the crucifer Barbarea vulgaris: Structural profile and correlation with glucosinolate turnover
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114872openalex-snapshot
SUPERROOT1 is not the only C–S lyase capable to contribute to glucosinolate biosynthesis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115108openalex-snapshot
Artefacts in natural products chemistry: formation mechanisms and avoidance strategies
inferred← citeshttps://doi.org/10.1038/s41564-021-00941-9openalex-snapshot
Host preference and invasiveness of commensal bacteria in the Lotus and Arabidopsis root microbiota
inferred← citeshttps://doi.org/10.1038/s42003-020-01523-xopenalex-snapshot
Brassicaceae transcriptomes reveal convergent evolution of super-accumulation of sinigrin
inferred← citeshttps://doi.org/10.1079/9781800629622.0006openalex-snapshot
Biometabolomics Resistance and Introgression of Host Resistance
inferred← citeshttps://doi.org/10.1080/07060661.2020.1775705openalex-snapshot
Transcriptome analysis of two lines of Brassica oleracea in response to early infection with Xanthomonas campestris pv. campestris
inferred← citeshttps://doi.org/10.1093/hr/uhad204openalex-snapshot
Unveiling plant defense arsenal: metabolic strategies in Brassica oleracea during black rot disease
inferred← citeshttps://doi.org/10.1093/jxb/erac240openalex-snapshot
The peptide SCOOP12 acts on reactive oxygen species homeostasis to modulate cell division and elongation in Arabidopsis primary root
inferred← citeshttps://doi.org/10.1093/pcp/pcac142openalex-snapshot
Loss of MYB34 Transcription Factor Supports the Backward Evolution of Indole Glucosinolate Biosynthesis in a Subclade of the Camelineae Tribe and Releases the Feedback Loop in This Pathway in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcy082openalex-snapshot
Specialized Vacuoles of Myrosin Cells: Chemical Defense Strategy in Brassicales Plants
inferred← citeshttps://doi.org/10.1093/plcell/koac255openalex-snapshot
AIG2A and AIG2B limit the activation of salicylic acid-regulated defenses by tryptophan-derived secondary metabolism in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiab011openalex-snapshot
Ubiquitylome analysis reveals a central role for the ubiquitin-proteasome system in plant innate immunity
inferred← citeshttps://doi.org/10.1094/mpmi-08-20-0233-ropenalex-snapshot
A Network of Phosphate Starvation and Immune-Related Signaling and Metabolic Pathways Controls the Interaction between Arabidopsis thaliana and the Beneficial Fungus Colletotrichum tofieldiae
inferred← citeshttps://doi.org/10.1101/2022.06.29.496778openalex-snapshot
Loss of MYB34 transcription factor that controls feedback loop in indole glucosinolate biosynthesis supports backward evolution of this pathway within Camelineae tribe
inferred← citeshttps://doi.org/10.1101/568113openalex-snapshot
Arabidopsis phytochelatin synthase 1, but not phytochelatin synthesis, functions in extracellular defense against multiple fungal pathogens
inferred← citeshttps://doi.org/10.1104/pp.17.01455openalex-snapshot
Glutathione Transferase U13 Functions in Pathogen-Triggered Glucosinolate Metabolism
inferred← citeshttps://doi.org/10.1111/nph.16118openalex-snapshot
The role of CYP 71A12 monooxygenase in pathogen‐triggered tryptophan metabolism and Arabidopsis immunity
inferred← citeshttps://doi.org/10.1111/nph.16918openalex-snapshot
Arabidopsis thaliana transcription factors MYB28 and MYB29 shape ammonium stress responses by regulating Fe homeostasis
inferred← citeshttps://doi.org/10.1111/tpj.13773openalex-snapshot
Plant–arthropod interactions: who is the winner?
inferred← citeshttps://doi.org/10.1128/spectrum.00180-21openalex-snapshot
Sclerotinia sclerotiorum Response to Long Exposure to Glucosinolate Hydrolysis Products by Transcriptomic Approach
inferred← citeshttps://doi.org/10.21203/rs.3.rs-145054/v1openalex-snapshot
Response of Sclerotinia Sclerotiorum to Long Exposure of Isothiocyanates by Transcriptomics Approach
inferred← citeshttps://doi.org/10.2174/1570163819666220615142933openalex-snapshot
In silico Prediction and Pharmacokinetic Studies on Glucosinolates as a Potential Drug and Key Inhibitor Molecule for Lanosterol-14α- demethylase: A Fungal Membrane Biosynthesis Enzyme
inferred← citeshttps://doi.org/10.26434/chemrxiv.13681603openalex-snapshot
Benzyl and Phenyl Glucosinolates Are Metabolized by the Specific Plant Pathogen Alternaria Brassicicola but Not by the Generalist Fungal Pathogens Rhizoctonia Solani or Sclerotinia Sclerotiorum
inferred← citeshttps://doi.org/10.26434/chemrxiv.13681603.v1openalex-snapshot
Benzyl and Phenyl Glucosinolates Are Metabolized by the Specific Plant Pathogen Alternaria Brassicicola but Not by the Generalist Fungal Pathogens Rhizoctonia Solani or Sclerotinia Sclerotiorum
inferred← citeshttps://doi.org/10.26434/chemrxiv.14166866openalex-snapshot
Phytoalexins and Signalling Metabolites Produced in the Wild Crucifer Neslia Paniculata: Camalexins and Arabidopsides
inferred← citeshttps://doi.org/10.26434/chemrxiv.14166866.v1openalex-snapshot
Phytoalexins and Signalling Metabolites Produced in the Wild Crucifer Neslia Paniculata: Camalexins and Arabidopsides
inferred← citeshttps://doi.org/10.26434/chemrxiv.14166866.v2openalex-snapshot
Phytoalexins and Signalling Metabolites Produced in the Wild Crucifer Neslia Paniculata: Camalexins and Arabidopsides
inferred← citeshttps://doi.org/10.3389/fpls.2018.01639openalex-snapshot
Glutathione S-Transferases in the Biosynthesis of Sulfur-Containing Secondary Metabolites in Brassicaceae Plants
inferred← citeshttps://doi.org/10.3389/fpls.2019.01008openalex-snapshot
Atypical Myrosinase as a Mediator of Glucosinolate Functions in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2019.01560openalex-snapshot
Coordination of Glucosinolate Biosynthesis and Turnover Under Different Nutrient Conditions
inferred← citeshttps://doi.org/10.3389/fpls.2021.829541openalex-snapshot
The Cell Differentiation of Idioblast Myrosin Cells: Similarities With Vascular and Guard Cells
inferred← citeshttps://doi.org/10.3389/fpls.2022.852808openalex-snapshot
The MIK2/SCOOP Signaling System Contributes to Arabidopsis Resistance Against Herbivory by Modulating Jasmonate and Indole Glucosinolate Biosynthesis
inferred← citeshttps://doi.org/10.3389/fpls.2022.932288openalex-snapshot
Fungal endophytes of Brassicaceae: Molecular interactions and crop benefits
inferred← citeshttps://doi.org/10.3389/fpls.2025.1701640openalex-snapshot
Proximity labelling suggests association of the nonhost receptor PSS1 protein with enzymes of multiple defense pathways in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms22010447openalex-snapshot
Evolution of A bHLH Interaction Motif
inferred← citeshttps://doi.org/10.3390/ijms22095004openalex-snapshot
Photoperiod Following Inoculation of Arabidopsis with Pyricularia oryzae (syn. Magnaporthe oryzae) Influences on the Plant–Pathogen Interaction
inferred← citeshttps://doi.org/10.3390/ijms242216356openalex-snapshot
The Homeodomain–Leucine Zipper Subfamily I Contributes to Leaf Age- and Time-Dependent Resistance to Pathogens in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/molecules27228042openalex-snapshot
The Impact of Nitrile-Specifier Proteins on Indolic Carbinol and Nitrile Formation in Homogenates of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants10061097openalex-snapshot
The Roles of Cruciferae Glucosinolates in Disease and Pest Resistance
inferred← citeshttps://doi.org/10.3390/plants10081656openalex-snapshot
Transcriptomic Reprograming of Xanthomonas campestris pv. campestris after Treatment with Hydrolytic Products Derived from Glucosinolates
inferred← citeshttps://doi.org/10.3390/plants9081006openalex-snapshot
Tumorous Stem Development of Brassica Juncea: A Complex Regulatory Network of Stem Formation and Identification of Key Genes in Glucosinolate Biosynthesis
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