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Atypical Myrosinase as a Mediator of Glucosinolate Functions in Plants
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0010(199703)73:3<364::aid-jsfa742>3.0.co;2-oopenalex-snapshot
Daily Variation in Glucosinolate Concentrations in the Leaves and Roots of Cabbage Seedlings in Two Constant Temperature Regimes
inferredcites →https://doi.org/10.1002/anie.201402639openalex-snapshot
Reactivity and Stability of Glucosinolates and Their Breakdown Products in Foods
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/10.1002/jpln.200520574openalex-snapshot
Impact of sulfate nutrition on the utilization of atmospheric SO2 as sulfur source for Chinese cabbage
inferredcites →https://doi.org/10.1007/978-3-319-25462-3_12openalex-snapshot
Investigation of Glucosinolates by Mass Spectrometry
inferredcites →https://doi.org/10.1007/978-3-319-25462-3_19openalex-snapshot
Therapeutic Paradigm Underscoring Glucosinolate Sulforaphane in Chemo- and Radiosensitization of Cancer: Preclinical and Clinical Perspective
inferredcites →https://doi.org/10.1007/978-3-319-32423-4_5openalex-snapshot
The Role of Abscisic Acid in Drought Stress: How ABA Helps Plants to Cope with Drought Stress
inferredcites →https://doi.org/10.1007/978-3-642-38797-5_2openalex-snapshot
ABA as a Universal Plant Hormone
inferredcites →https://doi.org/10.1007/978-94-011-4221-2_5openalex-snapshot
Myrosinase: gene family evolution and herbivore defense in Brassicaceae
inferredcites →https://doi.org/10.1007/978-94-017-0289-8_18openalex-snapshot
Sulphur Nutrition and Oilseed Quality
inferredcites →https://doi.org/10.1007/s10725-012-9748-5openalex-snapshot
Administration of isothiocyanates enhances heat tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11103-004-0790-1openalex-snapshot
Functional genomic analysis of Arabidopsis thaliana glycoside hydrolase family 1
inferredcites →https://doi.org/10.1016/b978-0-12-800876-8.00012-6openalex-snapshot
Role of Glucosinolates in Plant Stress Tolerance
inferredcites →https://doi.org/10.1016/bs.abr.2016.06.001openalex-snapshot
Complex Environments Interact With Plant Development to Shape Glucosinolate Profiles
inferredcites →https://doi.org/10.1016/bs.abr.2016.06.002openalex-snapshot
Nonlinear Selection and a Blend of Convergent, Divergent and Parallel Evolution Shapes Natural Variation in Glucosinolates
inferredcites →https://doi.org/10.1016/bs.abr.2016.06.004openalex-snapshot
Health Benefits of Glucosinolates
inferredcites →https://doi.org/10.1016/bs.abr.2016.06.005openalex-snapshot
Glucosinolate Regulation in a Complex Relationship – MYC and MYB – No One Can Act Without Each Other
inferredcites →https://doi.org/10.1016/bs.abr.2016.06.007openalex-snapshot
The Function of Glucosinolates and Related Metabolites in Plant Innate Immunity
inferredcites →https://doi.org/10.1016/bs.abr.2016.07.001openalex-snapshot
General Introduction to Glucosinolates
inferredcites →https://doi.org/10.1016/bs.abr.2016.07.003openalex-snapshot
Glucosinolates – The Agricultural Story
inferredcites →https://doi.org/10.1016/j.cell.2006.07.034openalex-snapshot
Activation of Glucosidase via Stress-Induced Polymerization Rapidly Increases Active Pools of Abscisic Acid
inferredcites →https://doi.org/10.1016/j.molp.2015.01.014openalex-snapshot
The Role of ABA Recycling and Transporter Proteins in Rapid Stomatal Responses to Reduced Air Humidity, Elevated CO2, and Exogenous ABA
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.2010.02.002openalex-snapshot
Regulatory networks of glucosinolates shape Arabidopsis thaliana fitness
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.pbi.2017.04.009openalex-snapshot
How does a plant orchestrate defense in time and space? Using glucosinolates in Arabidopsis as case study
inferredcites →https://doi.org/10.1016/j.phytochem.2009.07.036openalex-snapshot
Myrosinases from root and leaves of Arabidopsis thaliana have different catalytic properties
inferredcites →https://doi.org/10.1016/j.phytochem.2011.06.002openalex-snapshot
Metabolite profiling of Arabidopsis seedlings in response to exogenous sinalbin and sulfur deficiency
inferredcites →https://doi.org/10.1016/j.phytochem.2012.02.005openalex-snapshot
Glucosinolate structures in evolution
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.plantsci.2007.11.012openalex-snapshot
Leaf water balance mediated by aquaporins under salt stress and associated glucosinolate synthesis in broccoli
inferredcites →https://doi.org/10.1016/j.plantsci.2009.06.003openalex-snapshot
The two non-functional myrosinase genes TGG3 and TGG6 in Arabidopsis are expressed predominantly in pollen
inferredcites →https://doi.org/10.1016/j.plantsci.2009.09.013openalex-snapshot
Characterization of a root-specific β-thioglucoside glucohydrolase gene in Carica papaya and its recombinant protein expressed in Pichia pastoris
inferredcites →https://doi.org/10.1016/j.plantsci.2012.02.004openalex-snapshot
Properties of β-thioglucoside hydrolases (TGG1 and TGG2) from leaves of Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.tplants.2010.03.003openalex-snapshot
An expanding universe of circadian networks in higher plants
inferredcites →https://doi.org/10.1016/j.tplants.2015.04.006openalex-snapshot
Transport of defense compounds from source to sink: lessons learned from glucosinolates
inferredcites →https://doi.org/10.1016/j.ymeth.2011.06.005openalex-snapshot
Single-cell proteomic analysis of glucosinolate-rich S-cells in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0015-3796(84)80059-1openalex-snapshot
The mustard oil bomb: Rectified analysis of the subcellular organisation of the myrosinase system
inferredcites →https://doi.org/10.1016/s0031-9422(00)00316-2openalex-snapshot
The chemical diversity and distribution of glucosinolates and isothiocyanates among plants
inferredcites →https://doi.org/10.1016/s0031-9422(02)00549-6openalex-snapshot
Variation of glucosinolate accumulation among different organs and developmental stages of Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0065-2296(16)30101-xopenalex-snapshot
Advances in Botanical Research
inferredcites →https://doi.org/10.1016/s0969-2126(97)00221-9openalex-snapshot
The crystal structures of Sinapis alba myrosinase and a covalent glycosyl–enzyme intermediate provide insights into the substrate recognition and active-site machinery of an S-glycosidase
inferredcites →https://doi.org/10.1034/j.1399-3054.1997.990206.xopenalex-snapshot
Effect of chilling on the diurnal rhythm of enzymes involved in protection against oxidative stress in a chilling-tolerant and a chilling-sensitive maize genotype
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1110312.xopenalex-snapshot
Dark‐inducible genes from Arabidopsisthaliana are associated with leaf senescence and repressed by sugars
inferredcites →https://doi.org/10.1038/nature11285openalex-snapshot
NRT/PTR transporters are essential for translocation of glucosinolate defence compounds to seeds
inferredcites →https://doi.org/10.1038/nchembio.1914openalex-snapshot
Two cytochromes P450 catalyze S-heterocyclizations in cabbage phytoalexin biosynthesis
inferredcites →https://doi.org/10.1038/ng1543openalex-snapshot
A gene expression map of Arabidopsis thaliana development
inferredcites →https://doi.org/10.1038/s41598-018-28099-1openalex-snapshot
Arabidopsis mutants impaired in glutathione biosynthesis exhibit higher sensitivity towards the glucosinolate hydrolysis product allyl-isothiocyanate
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.1999.00573.xopenalex-snapshot
Light regulation of assimilatory sulphate reduction in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01636.xopenalex-snapshot
A novel ER‐derived compartment, the ER body, selectively accumulates a β‐glucosidase with an ER‐retention signal in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01657.xopenalex-snapshot
Transcriptome analysis of sulfur depletion in Arabidopsis thaliana: interlacing of biosynthetic pathways provides response specificity
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01658.xopenalex-snapshot
Global expression profiling of sulfur‐starved Arabidopsis by DNA macroarray reveals the role of O‐acetyl‐ l ‐serine as a general regulator of gene expression in response to sulfur nutrition
inferredcites →https://doi.org/10.1055/s-2007-965431openalex-snapshot
The Effect of Sulfur Nutrition on Plant Glucosinolate Content: Physiology and Molecular Mechanisms
inferredcites →https://doi.org/10.1073/pnas.0403218101openalex-snapshot
Integration of transcriptomics and metabolomics for understanding of global responses to nutritional stresses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1503926112openalex-snapshot
The butterfly plant arms-race escalated by gene and genome duplications
inferredcites →https://doi.org/10.1073/pnas.1615625114openalex-snapshot
Biosynthesis of cabbage phytoalexins from indole glucosinolate
inferredcites →https://doi.org/10.1074/jbc.m502332200openalex-snapshot
Elucidation of Gene-to-Gene and Metabolite-to-Gene Networks inArabidopsis by Integration of Metabolomics andTranscriptomics
inferredcites →https://doi.org/10.1080/07388551.2019.1576024openalex-snapshot
Myrosinase: insights on structural, catalytic, regulatory, and environmental interactions
inferredcites →https://doi.org/10.1093/jxb/erh184openalex-snapshot
Post-genomics approaches for the elucidation of plant adaptive mechanisms to sulphur deficiency
inferredcites →https://doi.org/10.1093/jxb/ers378openalex-snapshot
Diurnal and light regulation of sulphur assimilation and glucosinolate biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcm009openalex-snapshot
Glycosyl Hydrolases of Cell Wall are Induced by Sugar Starvation in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcn075openalex-snapshot
Antagonistic Jacalin-Related Lectins Regulate the Size of ER Body-Type β-Glucosidase Complexes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcp007openalex-snapshot
Constitutive and Inducible ER Bodies of Arabidopsis thaliana Accumulate Distinct β-Glucosidases
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/10.1093/pcp/pcp174openalex-snapshot
Scopolin-hydrolyzing -glucosidases in roots of Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcr156openalex-snapshot
Unique Defense Strategy by the Endoplasmic Reticulum Body in Plants
inferredcites →https://doi.org/10.1093/pcp/pcw037openalex-snapshot
Chemical Promotion of Endogenous Amounts of ABA inArabidopsis thalianaby a Natural Product, Theobroxide
inferredcites →https://doi.org/10.1093/pcp/pcx191openalex-snapshot
ATTED-II in 2018: A Plant Coexpression Database Based on Investigation of the Statistical Property of the Mutual Rank Index
inferredcites →https://doi.org/10.1093/pcp/pcy082openalex-snapshot
Specialized Vacuoles of Myrosin Cells: Chemical Defense Strategy in Brassicales Plants
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/10.1104/pp.001784openalex-snapshot
Cloning and Characterization of the Abscisic Acid-Specific Glucosyltransferase Gene from Adzuki Bean Seedlings
inferredcites →https://doi.org/10.1104/pp.009464openalex-snapshot
An Endoplasmic Reticulum-Derived Structure That Is Induced under Stress Conditions in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.102.019802openalex-snapshot
Transcriptome Profiling of Sulfur-Responsive Genes in Arabidopsis Reveals Global Effects of Sulfur Nutrition on Multiple Metabolic Pathways
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.123.3.949openalex-snapshot
A Glucosinolate Mutant of Arabidopsis Is Thermosensitive and Defective in Cytosolic Hsp90 Expression after Heat Stress
inferredcites →https://doi.org/10.1104/pp.126.2.811openalex-snapshot
Genetic Control of Natural Variation in Arabidopsis Glucosinolate Accumulation
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.15.00465openalex-snapshot
Large Cellular Inclusions Accumulate in Arabidopsis Roots Exposed to Low-Sulfur Conditions
inferredcites →https://doi.org/10.1104/pp.17.01455openalex-snapshot
Glutathione Transferase U13 Functions in Pathogen-Triggered Glucosinolate Metabolism
inferredcites →https://doi.org/10.1104/pp.18.00984openalex-snapshot
Leaf Endoplasmic Reticulum Bodies Identified in Arabidopsis Rosette Leaves Are Involved in Defense against Herbivory
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.010261openalex-snapshot
The Arabidopsis Epithiospecifier Protein Promotes the Hydrolysis of Glucosinolates to Nitriles and Influences Trichoplusia ni Herbivory
inferredcites →https://doi.org/10.1105/tpc.105.039339openalex-snapshot
BRANCHED-CHAIN AMINOTRANSFERASE4 Is Part of the Chain Elongation Pathway in the Biosynthesis of Methionine-Derived Glucosinolates in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.046458openalex-snapshot
Arabidopsis SLIM1 Is a Central Transcriptional Regulator of Plant Sulfur Response and Metabolism
inferredcites →https://doi.org/10.1105/tpc.106.047688openalex-snapshot
Analysis of Transcription Factor HY5 Genomic Binding Sites Revealed Its Hierarchical Role in Light Regulation of Development
inferredcites →https://doi.org/10.1105/tpc.106.048199openalex-snapshot
SLocus Genes and the Evolution of Self-Fertility inArabidopsis thaliana
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.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.112.095935openalex-snapshot
A Vacuolar β-Glucosidase Homolog That Possesses Glucose-Conjugated Abscisic Acid Hydrolyzing Activity Plays an Important Role in Osmotic Stress Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.12.2793openalex-snapshot
The Arabidopsis Epithiospecifier Protein Promotes the Hydrolysis of Glucosinolates to Nitriles and Influences Trichoplusia ni Herbivory
inferredcites →https://doi.org/10.1105/tpc.13.3.627openalex-snapshot
Self-Incompatibility in the Genus Arabidopsis: Characterization of the S Locus in the Outcrossing A. lyrata and Its Autogamous Relative A. thaliana
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.15.00946openalex-snapshot
Environmental Nitrate Stimulates Abscisic Acid Accumulation in Arabidopsis Root Tips by Releasing It from Inactive Stores
inferredcites →https://doi.org/10.1105/tpc.17.00073openalex-snapshot
ePlant: Visualizing and Exploring Multiple Levels of Data for Hypothesis Generation in Plant Biology
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.1365-313x.2005.02337.xopenalex-snapshot
Genome‐wide profiling of stored mRNA inArabidopsis thalianaseed germination: epigenetic and genetic regulation of transcription in seed
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.2007.03052.xopenalex-snapshot
The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV‐B light, drought and cold stress responses
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04656.xopenalex-snapshot
The key enzyme of sulfate assimilation, adenosine 5′‐phosphosulfate reductase, is regulated by HY5 in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.1988.tb02033.xopenalex-snapshot
Cysteine, γ‐glutamyl‐cysteine and glutathione contents of spinach leaves as affected by darkness and application of excess sulfur
inferredcites →https://doi.org/10.1111/j.1399-3054.1997.tb05409.xopenalex-snapshot
Effect of chilling on the diurnal rhythm of enzymes involved in protection against oxidative stress in a chilling‐tolerant and a chilling‐sensitive maize genotype
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/j.1742-4658.2005.05048.xopenalex-snapshot
The three desulfoglucosinolate sulfotransferase proteins in Arabidopsis have different substrate specificities and are differentially expressed
inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00988.xopenalex-snapshot
Characterization of a Novel β‐thioglucosidase CpTGG1 in Carica papaya and its Substrate‐dependent and Ascorbic Acid‐independent O‐β‐glucosidase Activity
inferredcites →https://doi.org/10.1111/ppl.12672openalex-snapshot
Localization of the glucosinolate biosynthetic enzymes reveals distinct spatial patterns for the biosynthesis of indole and aliphatic glucosinolates
inferredcites →https://doi.org/10.1111/tpj.12376openalex-snapshot
Aberrant gene expression in the A rabidopsis SULTR 1;2 mutants suggests a possible regulatory role for this sulfate transporter in response to sulfur nutrient status
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/10.1111/tpj.12824openalex-snapshot
The glucosinolate breakdown product indole‐3‐carbinol acts as an auxin antagonist in roots of A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.13377openalex-snapshot
PYK10 myrosinase reveals a functional coordination between endoplasmic reticulum bodies and glucosinolates in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.13610openalex-snapshot
Wounding of Arabidopsis leaves induces indole‐3‐carbinol‐dependent autophagy in roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.14327openalex-snapshot
Structural diversification during glucosinolate breakdown: mechanisms of thiocyanate, epithionitrile and simple nitrile formation
inferredcites →https://doi.org/10.1126/sciadv.1601087openalex-snapshot
Sulfur deficiency–induced repressor proteins optimize glucosinolate biosynthesis in plants
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.1143153openalex-snapshot
The Evolution of Selfing in 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-043014-114707openalex-snapshot
Diverse Stomatal Signaling and the Signal Integration Mechanism
inferredcites →https://doi.org/10.1146/annurev-arplant-050718-100152openalex-snapshot
Evolution of Glucosinolate Diversity via Whole-Genome Duplications, Gene Rearrangements, and Substrate Promiscuity
inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144046openalex-snapshot
ABSCISIC ACID BIOSYNTHESIS AND CATABOLISM
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105228openalex-snapshot
BIOLOGY AND BIOCHEMISTRY OF GLUCOSINOLATES
inferredcites →https://doi.org/10.1186/s12864-016-3039-xopenalex-snapshot
Allyl-isothiocyanate treatment induces a complex transcriptional reprogramming including heat stress, oxidative stress and plant defence responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/s13007-017-0164-8openalex-snapshot
Development of an efficient glucosinolate extraction method
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.0202153openalex-snapshot
Extended darkness induces internal turnover of glucosinolates in Arabidopsis thaliana leaves
inferredcites →https://doi.org/10.3389/fpls.2014.00073openalex-snapshot
ER bodies in plants of the Brassicales order: biogenesis and association with innate immunity
inferredcites →https://doi.org/10.3389/fpls.2015.00524openalex-snapshot
The impact of the absence of aliphatic glucosinolates on water transport under salt stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2016.00774openalex-snapshot
The Defense Metabolite, Allyl Glucosinolate, Modulates Arabidopsis thaliana Biomass Dependent upon the Endogenous Glucosinolate Pathway
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.2016.01821openalex-snapshot
NSP-Dependent Simple Nitrile Formation Dominates upon Breakdown of Major Aliphatic Glucosinolates in Roots, Seeds, and Seedlings of Arabidopsis thaliana Columbia-0
inferredcites →https://doi.org/10.3389/fpls.2017.00350openalex-snapshot
A Phylogenetically Informed Comparison of GH1 Hydrolases between Arabidopsis and Rice Response to Stressors
inferredcites →https://doi.org/10.3389/fpls.2017.02131openalex-snapshot
Possible Interactions between the Biosynthetic Pathways of Indole Glucosinolate and Auxin
inferredcites →https://doi.org/10.3389/fpls.2018.00550openalex-snapshot
Dynamic Modeling of Indole Glucosinolate Hydrolysis and Its Impact on Auxin Signaling
inferredcites →https://doi.org/10.3389/fpls.2018.01240openalex-snapshot
Benzyl Cyanide Leads to Auxin-Like Effects Through the Action of Nitrilases in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2019.00618openalex-snapshot
Chemodiversity of the Glucosinolate-Myrosinase System at the Single Cell Type Resolution
inferredcites →https://doi.org/10.3390/ijms140611607openalex-snapshot
The Physiological Importance of Glucosinolates on Plant Response to Abiotic Stress in Brassica
inferredcites →https://doi.org/10.3390/ijms17020262openalex-snapshot
Identification and Evolution of Functional Alleles of the Previously Described Pollen Specific Myrosinase Pseudogene AtTGG6 in Arabidopsis thaliana
inferredcites →https://doi.org/10.3390/ijms17060892openalex-snapshot
Arabidopsis Myrosinase Genes AtTGG4 and AtTGG5 Are Root-Tip Specific and Contribute to Auxin Biosynthesis and Root-Growth Regulation
inferredcites →https://doi.org/10.3390/ijms18112372openalex-snapshot
Glucosinolate-Derived Isothiocyanates Inhibit Arabidopsis Growth and the Potency Depends on Their Side Chain Structure
inferredcites →https://doi.org/10.7554/elife.29353openalex-snapshot
An evolutionarily young defense metabolite influences the root growth of plants via the ancient TOR signaling pathway
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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/bab.2400openalex-snapshot
Development of a “turn off–on” whole‐cell biosensor for sulforaphane detection based on the ultrasensitive activator HrpRS
inferred← citeshttps://doi.org/10.1007/s00425-024-04391-5openalex-snapshot
Multifaceted roles of plant glycosyl hydrolases during pathogen infections: more to discover
inferred← citeshttps://doi.org/10.1007/s11101-020-09699-0openalex-snapshot
Natural control of plant pathogens through glucosinolates: an effective strategy against fungi and oomycetes
inferred← citeshttps://doi.org/10.1016/b978-0-12-822845-6.00004-xopenalex-snapshot
Modeling quality attributes and quality-related product properties
inferred← citeshttps://doi.org/10.1016/b978-0-12-824467-8.00013-9openalex-snapshot
Latest developments in quality control parameters/specifications in phytonutrients studies
inferred← citeshttps://doi.org/10.1016/j.aoas.2021.02.001openalex-snapshot
Studies on exogenous elicitors promotion of sulforaphane content in broccoli sprouts and its effect on the MDA-MB-231 breast cancer cell line
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2021.107784openalex-snapshot
Metabolic and biotransformation effects on dietary glucosinolates, their bioavailability, catabolism and biological effects in different organisms
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.139046openalex-snapshot
Overexpression of LSU1 and LSU2 confers cadmium tolerance by manipulating sulfur metabolism in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106409openalex-snapshot
Distinct contributions of cryptochromes and UVR8 to blue light signaling and root development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.fbio.2020.100814openalex-snapshot
The development of a broccoli supplemented beer allows obtaining a valuable dietary source of sulforaphane
inferred← citeshttps://doi.org/10.1016/j.fufo.2026.100991openalex-snapshot
Changes of nutraceutical traits in baby leaves of sprouting broccoli (Brassica oleracea L. var. italica Plenck) induced by Moringa spp. extracts
inferred← citeshttps://doi.org/10.1016/j.ibmb.2023.104040openalex-snapshot
Different myrosinases activate sequestered glucosinolates in larvae and adults of the horseradish flea beetle
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110764openalex-snapshot
Abscisic acid-mediated induction of FLAVIN-CONTAINING MONOOXYGENASE 2 leads to reduced accumulation of methylthioalkyl glucosinolates in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112023openalex-snapshot
N6-methyladenosine analysis unveils key mechanisms underlying long-term salt stress tolerance in switchgrass (Panicum virgatum)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112883openalex-snapshot
Regulatory mechanisms of ER body formation and its function in Brassicaceae plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108255openalex-snapshot
ECT12, an YTH-domain protein, is a potential mRNA m6A reader that affects abiotic stress responses by modulating mRNA stability in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.tifs.2026.105625openalex-snapshot
Microorganisms achieve the transformation of sulforaphane through active the synergistic action of myrosinase-like enzyme systems and transport networks
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c01916openalex-snapshot
A Comprehensive Gene Inventory for Glucosinolate Biosynthetic Pathway in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s41467-023-39800-yopenalex-snapshot
The allotetraploid horseradish genome provides insights into subgenome diversification and formation of critical traits
inferred← citeshttps://doi.org/10.1073/pnas.2017890118openalex-snapshot
Retrograde sulfur flow from glucosinolates to cysteine in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/15592324.2021.1966586openalex-snapshot
Metabolite analysis of Arabidopsis CYP79A2 overexpression lines reveals turnover of benzyl glucosinolate and an additive effect of different aldoximes on phenylpropanoid repression
inferred← citeshttps://doi.org/10.1080/19315260.2023.2170302openalex-snapshot
Methyl jasmonate and type of fertilization affect growth, production and accumulation of sulforaphane in black radish taproot
inferred← citeshttps://doi.org/10.1093/jxb/eraa420openalex-snapshot
Stomatal response to isothiocyanates inArabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/eraa479openalex-snapshot
Regulation of glucosinolate biosynthesis
inferred← citeshttps://doi.org/10.1093/pcp/pcac177openalex-snapshot
Endoplasmic Reticulum Bodies in the Lateral Root Cap Are Involved in the Direct Transport of Beta-Glucosidase to Vacuoles
inferred← citeshttps://doi.org/10.1093/plcell/koac185openalex-snapshot
Defects in autophagy lead to selective in vivo changes in turnover of cytosolic and organelle proteins in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiab247openalex-snapshot
Multiple indole glucosinolates and myrosinases defend Arabidopsis against Tetranychus urticae herbivory
inferred← citeshttps://doi.org/10.1093/plphys/kiab283openalex-snapshot
Jasmonate regulates the FAMA/mediator complex subunit 8-THIOGLUCOSIDE GLUCOHYDROLASE 1 cascade and myrosinase activity
inferred← citeshttps://doi.org/10.1094/mpmi-11-20-0330-scopenalex-snapshot
ER Bodies Are Induced by Pseudomonas syringae and Negatively Regulate Immunity
inferred← citeshttps://doi.org/10.1111/nph.18324openalex-snapshot
Specialist root herbivore modulates plant transcriptome and downregulates defensive secondary metabolites in a brassicaceous plant
inferred← citeshttps://doi.org/10.1111/pce.14870openalex-snapshot
Plant glucosinolate biosynthesis and breakdown pathways shape the rhizosphere bacterial/archaeal community
inferred← citeshttps://doi.org/10.1111/ppl.13505openalex-snapshot
Alpha‐ketoglutarate‐dependent dioxygenase homolog 10B, an N 6 ‐methyladenosine mRNA demethylase, plays a role in salt stress and abscisic acid responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.14878openalex-snapshot
flasher, a novel mutation in a glucosinolate modifying enzyme, conditions changes in plant architecture and hormone homeostasis
inferred← citeshttps://doi.org/10.1111/tpj.16370openalex-snapshot
Altered methionine metabolism impacts phenylpropanoid production and plant development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.17181openalex-snapshot
WHIRLY1 regulates aliphatic glucosinolate biosynthesis in early seedling development of Arabidopsis
inferred← citeshttps://doi.org/10.1186/s12870-026-08170-0openalex-snapshot
Comparative transcriptomic and transcript-based network analyses revealed genotype-specific alternative splicing induced by Sclerotinia sclerotiorum in Brassica napus
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.63.415openalex-snapshot
Apiose, A Branched Sugar Unique to Plants
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10032606/v1openalex-snapshot
Proton-anion exchange by a MATE transporter mediates high glucosinolate accumulation in Arabidopsis vacuoles
inferred← citeshttps://doi.org/10.2139/ssrn.5624056openalex-snapshot
Biostimulant Effects of Moringa spp. Extracts on baby leaves of Brassica oleracea L. var. italica Plenck
inferred← citeshttps://doi.org/10.3389/fmolb.2025.1607330openalex-snapshot
Phytonutrients and their neuroprotective role in brain disorders
inferred← citeshttps://doi.org/10.3389/fpls.2019.01549openalex-snapshot
Glucosinolate Content in Dormant and Germinating Arabidopsis thaliana Seeds Is Affected by Non-Functional Alleles of Classical Myrosinase and Nitrile-Specifier Protein Genes
inferred← citeshttps://doi.org/10.3389/fpls.2020.589746openalex-snapshot
Effect of Photoperiod on Chinese Kale (Brassica alboglabra) Sprouts Under White or Combined Red and Blue Light
inferred← citeshttps://doi.org/10.3389/fpls.2022.1025969openalex-snapshot
First experimental evidence suggests use of glucobrassicin as source of auxin in drought-stressed Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/agronomy10111786openalex-snapshot
Glucosinolate Biosynthesis and the Glucosinolate–Myrosinase System in Plant Defense
inferred← citeshttps://doi.org/10.3390/agronomy12102508openalex-snapshot
Understanding the Complex Functional Interplay between Glucosinolates and Cyanogenic Glycosides in Carica papaya
inferred← citeshttps://doi.org/10.3390/foods13050696openalex-snapshot
Application of Tryptophan and Methionine in Broccoli Seedlings Enhances Formation of Anticancer Compounds Sulforaphane and Indole-3-Carbinol and Promotes Growth
inferred← citeshttps://doi.org/10.3390/ijms23031577openalex-snapshot
The Cellular and Subcellular Organization of the Glucosinolate–Myrosinase System against Herbivores and Pathogens
inferred← citeshttps://doi.org/10.3390/ijms24044094openalex-snapshot
Metabolic Background, Not Photosynthetic Physiology, Determines Drought and Drought Recovery Responses in C3 and C2 Moricandias
inferred← citeshttps://doi.org/10.3390/ijms241713520openalex-snapshot
Overexpression of BoLSU1 and BoLSU2 Confers Tolerance to Sulfur Deficiency in Arabidopsis by Manipulating Glucosinolate Metabolism
inferred← citeshttps://doi.org/10.3390/ijms25169039openalex-snapshot
Brassicaceae Mustards: Phytochemical Constituents, Pharmacological Effects, and Mechanisms of Action against Human Disease
inferred← citeshttps://doi.org/10.3390/ijpb16020058openalex-snapshot
Glucosinolates in Cruciferous Vegetables: Genetic and Environmental Regulation, Metabolic Pathways, and Cancer-Preventive Mechanisms
inferred← citeshttps://doi.org/10.3390/jof9010052openalex-snapshot
Lignin and Its Pathway-Associated Phytoalexins Modulate Plant Defense against Fungi
inferred← citeshttps://doi.org/10.3390/nu14091712openalex-snapshot
Clinical Evidence of the Benefits of Phytonutrients in Human Healthcare
inferred← citeshttps://doi.org/10.3390/plants12020266openalex-snapshot
Occurrence, Function, and Biosynthesis of the Natural Auxin Phenylacetic Acid (PAA) in Plants
inferred← citeshttps://doi.org/10.3390/plants14142129openalex-snapshot
Impacts of Sulfur on Glucosinolate Metabolism: From Arabidopsis to Wild Brassicales
inferred← citeshttps://doi.org/10.3390/plants9121705openalex-snapshot
The Versatile Roles of Sulfur-Containing Biomolecules in Plant Defense—A Road to Disease Resistance
inferred← citeshttps://doi.org/10.47836/mjmhs20.5.34openalex-snapshot
Impact of Glucosinolates Intervention in Controlling the Progression of Cancer: A Systematic Review of a Randomized Controlled Trial
inferred← citeshttps://doi.org/10.64898/2026.08.10.742692openalex-snapshot
Loss of a conserved disulfide bond defines Penetration2-related immune myrosinases in Brassicaceae
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