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JASMONATE-INSENSITIVE1 Encodes a MYC Transcription Factor Essential to Discriminate between Different Jasmonate-Regulated Defense Responses in Arabidopsis[W]
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/geno.1994.1023openalex-snapshot
Assignment of 30 Microsatellite Loci to the Linkage Map of Arabidopsis
inferredcites →https://doi.org/10.1007/s00344-003-0027-6openalex-snapshot
Interactions Between Signaling Compounds Involved in Plant Defense
inferredcites →https://doi.org/10.1007/s00425-001-0688-yopenalex-snapshot
Jasmonate-related mutants of Arabidopsis as tools for studying stress signaling
inferredcites →https://doi.org/10.1007/s00425-002-0787-4openalex-snapshot
A conditionally fertile coi1 allele indicates cross-talk between plant hormone signalling pathways in Arabidopsis thaliana seeds and young seedlings
inferredcites →https://doi.org/10.1016/s0014-5793(01)02331-6openalex-snapshot
An Arabidopsis mutant cex1 exhibits constant accumulation of jasmonate‐regulated AtVSP, Thi2.1 and PDF1.2
inferredcites →https://doi.org/10.1016/s0092-8674(00)00213-0openalex-snapshot
Arabidopsis MAP Kinase 4 Negatively Regulates Systemic Acquired Resistance
inferredcites →https://doi.org/10.1016/s0168-9525(96)10049-4openalex-snapshot
MYB transcription factors in plants
inferredcites →https://doi.org/10.1016/s0952-7915(00)00183-7openalex-snapshot
The complexity of disease signaling in Arabidopsis
inferredcites →https://doi.org/10.1016/s1369-5266(03)00045-1openalex-snapshot
Jasmonates and related oxylipins in plant responses to pathogenesis and herbivory
inferredcites →https://doi.org/10.1016/s1369-5266(98)80264-1openalex-snapshot
Jasmonate and salicylate as global signals for defense gene expression
inferredcites →https://doi.org/10.1034/j.1399-3054.1997.1000329.xopenalex-snapshot
Enzymes involved in jasmonic acid biosynthesis
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01241.xopenalex-snapshot
Fusion genetic analysis of jasmonate‐signalling mutants in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.1993.04020403.xopenalex-snapshot
A procedure for mapping Arabidopsis mutations using co‐dominant ecotype‐specific PCR‐based markers
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00261.xopenalex-snapshot
Expression of the Arabidopsisabi1–1mutant allele inhibits proteinase inhibitor wound‐induction in tomato
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00265.xopenalex-snapshot
Jasmonate signaling mutants ofArabidopsisare susceptible to the soil fungusPythium irregulare
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00570.xopenalex-snapshot
Cross‐talk between wound signalling pathways determines local versus systemic gene expression in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.2641036.xopenalex-snapshot
Isolation and characterization of signal transduction mutants of Arabidopsis thaliana that constitutively activate the octadecanoid pathway and form necrotic microlesions
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01191.xopenalex-snapshot
Constitutive expression of ETHYLENE‐RESPONSE‐FACTOR1 in Arabidopsis confers resistance to several necrotrophic fungi
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01432.xopenalex-snapshot
COI1 links jasmonate signalling and fertility to the SCF ubiquitin–ligase complex in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01434.xopenalex-snapshot
Ozone‐induced ethylene production is dependent on salicylic acid, and both salicylic acid and ethylene act in concert to regulate ozone‐induced cell death
inferredcites →https://doi.org/10.1073/pnas.250379897openalex-snapshot
Identification of the residues in the Myb domain of maize C1 that specify the interaction with the bHLH cofactor R
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/10.1073/pnas.92.10.4106openalex-snapshot
Signals involved in wound-induced proteinase inhibitor II gene expression in tomato and potato plants.
inferredcites →https://doi.org/10.1073/pnas.94.10.5473openalex-snapshot
Jasmonate is essential for insect defense in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.95.25.15107openalex-snapshot
Separate jasmonate-dependent and salicylate-dependent defense-response pathways in Arabidopsis are essential for resistance to distinct microbial pathogens
inferredcites →https://doi.org/10.1093/genetics/156.3.1349openalex-snapshot
GL3 Encodes a bHLH Protein That Regulates Trichome Development in Arabidopsis Through Interaction With GL1 and TTG1
inferredcites →https://doi.org/10.1093/genetics/161.3.1235openalex-snapshot
Dominant Alleles of the Basic Helix-Loop-Helix Transcription Factor ATR2 Activate Stress-Responsive Genes in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erg123openalex-snapshot
A jasmonate‐responsive element within the A. thaliana vsp1 promoter
inferredcites →https://doi.org/10.1093/nar/13.13.4777openalex-snapshot
Efficient octopine Ti plasmid-derived vectors for Agrobacterium -mediated gene transfer to plants
inferredcites →https://doi.org/10.1104/pp.002857openalex-snapshot
Transcriptional Profiling Reveals Novel Interactions between Wounding, Pathogen, Abiotic Stress, and Hormonal Responses in Arabidopsis,
inferredcites →https://doi.org/10.1104/pp.005272openalex-snapshot
An Arabidopsis Mutant Defective in Jasmonate Response Is Allelic to the Auxin-Signaling Mutant axr1
inferredcites →https://doi.org/10.1104/pp.102.017814openalex-snapshot
A Role for the GCC-Box in Jasmonate-Mediated Activation of the PDF1.2 Gene of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.2.525openalex-snapshot
Two Methyl Jasmonate-Insensitive Mutants Show Altered Expression of AtVsp in Response to Methyl Jasmonate and Wounding
inferredcites →https://doi.org/10.1104/pp.112.2.525openalex-snapshot
Tissue-Specific Activity of Two Manganese Superoxide Dismutase Promoters in Transgenic Tobacco
inferredcites →https://doi.org/10.1104/pp.112.3.893openalex-snapshot
An Improved Green Fluorescent Protein Gene as a Vital Marker in Plants
inferredcites →https://doi.org/10.1104/pp.119.3.1065openalex-snapshot
Embryo-Specific Gene Expression in Microspore-Derived Embryos ofBrassica napus.An Interaction between Abscisic Acid and Jasmonic Acid1,2
inferredcites →https://doi.org/10.1104/pp.95.2.399openalex-snapshot
Effects of Jasmonic Acid on Embryo-Specific Processes in Brassica and Linum Oilseeds
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.002022openalex-snapshot
The Arabidopsis Mutant cev1 Links Cell Wall Signaling to Jasmonate and Ethylene Responses
inferredcites →https://doi.org/10.1105/tpc.003368openalex-snapshot
The SCF COI1 Ubiquitin-Ligase Complexes Are Required for Jasmonate Response in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.006130openalex-snapshot
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.007468openalex-snapshot
ETHYLENE RESPONSE FACTOR1 Integrates Signals from Ethylene and Jasmonate Pathways in Plant Defense[W]
inferredcites →https://doi.org/10.1105/tpc.010207openalex-snapshot
The COP9 Signalosome Interacts Physically with SCFCOI1 and Modulates Jasmonate Responses
inferredcites →https://doi.org/10.1105/tpc.017954openalex-snapshot
The Tomato Homolog of CORONATINE-INSENSITIVE1 Is Required for the Maternal Control of Seed Maturation, Jasmonate-Signaled Defense Responses, and Glandular Trichome Development[W]
inferredcites →https://doi.org/10.1105/tpc.10.12.2103openalex-snapshot
Concomitant Activation of Jasmonate and Ethylene Response Pathways Is Required for Induction of a Plant Defensin Gene in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.10.9.1571openalex-snapshot
A Novel Signaling Pathway Controlling Induced Systemic Resistance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.12.10.1849openalex-snapshot
Ozone-Sensitive Arabidopsis rcd1 Mutant Reveals Opposite Roles for Ethylene and Jasmonate Signaling Pathways in Regulating Superoxide-Dependent Cell Death
inferredcites →https://doi.org/10.1105/tpc.12.5.707openalex-snapshot
Differential Gene Expression in Response to Mechanical Wounding and Insect Feeding in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.5.1025openalex-snapshot
The Arabidopsis Mutant cev1 Has Constitutively Active Jasmonate and Ethylene Signal Pathways and Enhanced Resistance to Pathogens
inferredcites →https://doi.org/10.1105/tpc.4.9.1157openalex-snapshot
General roles of abscisic and jasmonic acids in gene activation as a result of mechanical wounding.
inferredcites →https://doi.org/10.1105/tpc.6.5.751openalex-snapshot
Arabidopsis Mutants Selected for Resistance to the Phytotoxin Coronatine Are Male Sterile, Insensitive to Methyl Jasmonate, and Resistant to a Bacterial Pathogen.
inferredcites →https://doi.org/10.1105/tpc.8.12.2309openalex-snapshot
Pathogen-induced systemic activation of a plant defensin gene in Arabidopsis follows a salicylic acid-independent pathway.
inferredcites →https://doi.org/10.1105/tpc.9.10.1859openalex-snapshot
Role of arabidopsis MYC and MYB homologs in drought- and abscisic acid-regulated gene expression.
inferredcites →https://doi.org/10.1105/tpc.9.12.2243openalex-snapshot
Antagonistic effects of abscisic acid and jasmonates on salt stress-inducible transcripts in rice roots.
inferredcites →https://doi.org/10.1105/tpc.9.7.1211openalex-snapshot
Oligosaccharins, brassinolides, and jasmonates: nontraditional regulators of plant growth, development, and gene expression.
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.280.5366.1091openalex-snapshot
COI1 : An Arabidopsis Gene Required for Jasmonate-Regulated Defense and Fertility
inferredcites →https://doi.org/10.1126/science.289.5477.295openalex-snapshot
ORCA3, a Jasmonate-Responsive Transcriptional Regulator of Plant Primary and Secondary Metabolism
inferredcites →https://doi.org/10.2307/3871197openalex-snapshot
Ozone-Sensitive Arabidopsis rcd1 Mutant Reveals Opposite Roles for Ethylene and Jasmonate Signaling Pathways in Regulating Superoxide-Dependent Cell Death
inferredcites →https://doi.org/10.2307/3871361openalex-snapshot
The Arabidopsis Mutant cev1 Has Constitutively Active Jasmonate and Ethylene Signal Pathways and Enhanced Resistance to Pathogens
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4651465openalex-extracted
Jasmonates Play a Core Role in Key Oolong Tea Aroma Differential Accumulation in Two Tea Varieties (Camellia Sinensis) Postharvest Leaves after Mechanical Stress
inferred← citeshttps://doi.org/10.1002/2211-5463.13619openalex-snapshot
Specificity models in MAPK cascade signaling
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020138openalex-snapshot
Jasmonate Synthesis and Action in Higher Plants
inferred← citeshttps://doi.org/10.1002/9780470015902.a0023721openalex-snapshot
Jasmonic Acid Signalling
inferred← citeshttps://doi.org/10.1002/9780470988800.ch7openalex-snapshot
Oxylipins: Biosynthesis, Signal Transduction and Action
inferred← citeshttps://doi.org/10.1002/9780470988886.ch11openalex-snapshot
Networks of Transcriptional Regulation Underlying Plant Defense Responses Toward Phytopathogens
inferred← citeshttps://doi.org/10.1002/9780470995983.ch3openalex-snapshot
Genomics in Induced Resistance
inferred← citeshttps://doi.org/10.1002/9780470995983.ch4openalex-snapshot
Signalling Cascades Involved in Induced Resistance
inferred← citeshttps://doi.org/10.1002/9780813805931.ch1openalex-snapshot
Role of Abscisic Acid in Disease Resistance
inferred← citeshttps://doi.org/10.1002/9781118223086.ch12openalex-snapshot
Ethylene and Senescence Processes
inferred← citeshttps://doi.org/10.1002/9781118371848.ch3openalex-snapshot
Transcriptome Analysis of Induced Resistance
inferred← citeshttps://doi.org/10.1002/9781118371848.ch4openalex-snapshot
Signalling Networks Involved in Induced Resistance
inferred← citeshttps://doi.org/10.1002/9781118481431.ch12openalex-snapshot
Future Prospects for Genetically Engineering Disease‐Resistant Plants
inferred← citeshttps://doi.org/10.1002/9781118481431.ch4openalex-snapshot
The Roles of Salicylic Acid and Jasmonic Acid in Plant Immunity
inferred← citeshttps://doi.org/10.1002/9781118801512.ch14openalex-snapshot
Harnessing Plant Trichome Biochemistry for the Production of Useful Compounds
inferred← citeshttps://doi.org/10.1002/9781118829783.ch5openalex-snapshot
Plant Transcriptomic Responses to Herbivory
inferred← citeshttps://doi.org/10.1002/9781118889022.ch28openalex-snapshot
Convergence of Stress‐Induced Hormone Signaling Pathways on a Transcriptional Co‐Factor
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0248openalex-snapshot
Oxylipins: Biosynthesis, Signal Transduction and Action
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0306openalex-snapshot
Networks of Transcriptional Regulation Underlying Plant Defense Responses toward Phytopathogens
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0350openalex-snapshot
Mitogen‐Activated Protein Kinase Cascades in Plant Signaling
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0370openalex-snapshot
Lipid Signals in Plant–Pathogen Interactions
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0371openalex-snapshot
Induced Resistance – Orchestrating Defence Mechanisms through Crosstalk and Priming
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0484openalex-snapshot
Ethylene and Senescence Processes
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0509openalex-snapshot
Plant Transcriptomic Responses to Herbivory
inferred← citeshttps://doi.org/10.1002/9781119409144.ch51openalex-snapshot
Leaf me alone:Medicago truncatuladefenses against foliar lepidopteran herbivores
inferred← citeshttps://doi.org/10.1002/9781119858553.ch19openalex-snapshot
Phytohormones as a Novel Weapon in Management of Plant Stress Against Biotic Agents
inferred← citeshttps://doi.org/10.1002/9781444301441.ch10openalex-snapshot
Lipid Signals in Plant–Pathogen Interactions
inferred← citeshttps://doi.org/10.1002/9781444301441.ch11openalex-snapshot
Induced Resistance– Orchestrating Defence Mechanisms through Crosstalk and Priming
inferred← citeshttps://doi.org/10.1002/9783527628964.ch4openalex-snapshot
Stress Physiology of Higher Plants: Cross‐Talk between Abiotic and Biotic Stress Signaling
inferred← citeshttps://doi.org/10.1002/9783527628964.ch5openalex-snapshot
Jasmonates in Stress, Growth, and Development
inferred← citeshttps://doi.org/10.1002/advs.202521040openalex-snapshot
Plant Genetic Engineering: Technological Pathways, Application Scenarios, and Future Directions
inferred← citeshttps://doi.org/10.1002/csc2.70210openalex-snapshot
Abscisic acid and jasmonic acid crosstalk regulates seedling salt tolerance in rice varieties with different salinity tolerances
inferred← citeshttps://doi.org/10.1002/pld3.177openalex-snapshot
MYC2 regulates ARR16, a component of cytokinin signaling pathways, in Arabidopsis seedling development
inferred← citeshttps://doi.org/10.1002/pld3.70042openalex-snapshot
Unequal Genetic Redundancies Among MYC bHLH Transcription Factors Underlie Seedling Photomorphogenesis in Arabidopsis
inferred← citeshttps://doi.org/10.1002/pld3.70170openalex-snapshot
Gene Expression Patterns Regulating Peanut Reproductive Phenology
inferred← citeshttps://doi.org/10.1002/ps.5681openalex-snapshot
The interactions of PhSPL17 and PhJAZ1 mediate the on‐ and off‐year moso bamboo ( Phyllostachys heterocycla ) resistance to the Pantana phyllostachysae larval feeding
inferred← citeshttps://doi.org/10.1002/ps.8618openalex-snapshot
CeJAZ3 suppresses longifolene accumulation in Casuarina equisetifolia, affecting the host preference of Anoplophora chinensis
inferred← citeshttps://doi.org/10.1002/tpg2.20502openalex-snapshot
Identification of the sweet orange ( Citrus sinensis ) bHLH gene family and the role of CsbHLH55 and CsbHLH87 in regulating salt stress
inferred← citeshttps://doi.org/10.1007/978-0-387-85498-4_8openalex-snapshot
Regulation of Secondary Metabolism by Jasmonate Hormones
inferred← citeshttps://doi.org/10.1007/978-1-0716-0142-6_9openalex-snapshot
Establishment of Actinorhizal Symbiosis in Response to Ethylene, Salicylic Acid, and Jasmonate
inferred← citeshttps://doi.org/10.1007/978-1-0716-1609-3_6openalex-snapshot
DAP-Seq Identification of Transcription Factor-Binding Sites in Potato
inferred← citeshttps://doi.org/10.1007/978-1-4020-8182-8_17openalex-snapshot
Jasmonate Biosynthesis and Signaling for Induced Plant Defense against Herbivory
inferred← citeshttps://doi.org/10.1007/978-1-4020-8930-5_2openalex-snapshot
Mechanisms of Induced Resistance Against B. cinerea
inferred← citeshttps://doi.org/10.1007/978-1-4614-6372-6_2openalex-snapshot
Biotic and Abiotic Stress Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-1-4614-8600-8_4openalex-snapshot
Major Phytohormones Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-1-4939-0491-4_10openalex-snapshot
Phytohormonal Crosstalk Under Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-1-4939-0491-4_8openalex-snapshot
Jasmonates in Plant Growth and Stress Responses
inferred← citeshttps://doi.org/10.1007/978-1-61779-154-3_11openalex-snapshot
Isolation of Transcription Factor Complexes from Arabidopsis Cell Suspension Cultures by Tandem Affinity Purification
inferred← citeshttps://doi.org/10.1007/978-1-62703-414-2_16openalex-snapshot
Agroinfiltration of Nicotiana benthamiana Leaves for Co-localization of Regulatory Proteins Involved in Jasmonate Signaling
inferred← citeshttps://doi.org/10.1007/978-1-62703-414-2_4openalex-snapshot
Bioassays for Assessing Jasmonate-Dependent Defenses Triggered by Pathogens, Herbivorous Insects, or Beneficial Rhizobacteria
inferred← citeshttps://doi.org/10.1007/978-3-030-75805-9_7openalex-snapshot
Jasmonate: A Versatile Messenger in Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-77477-6_1openalex-snapshot
Plant Hormones and Plant Defense Response Against Pathogens
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_17openalex-snapshot
Jasmonates: A Thorough Insight into the Mechanism of Biosynthesis, Signaling and Action in Root Growth and Development
inferred← citeshttps://doi.org/10.1007/978-3-031-12990-2_10openalex-snapshot
The Role of Transcription Factors in Response to Biotic Stresses in Pearl Millet
inferred← citeshttps://doi.org/10.1007/978-3-319-26118-8_6openalex-snapshot
Molecular Manipulation of Transcription Factors, the Master Regulators of PAMP-Triggered Signaling Systems
inferred← citeshttps://doi.org/10.1007/978-3-319-91352-0_5openalex-snapshot
Structural Biology of Jasmonic Acid Metabolism and Responses in Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-96971-8_15openalex-snapshot
Diversity, Ecology, and Conservation of Fungal and Bacterial Endophytes
inferred← citeshttps://doi.org/10.1007/978-3-540-87407-2_17openalex-snapshot
Signal Perception and Transduction in Plants
inferred← citeshttps://doi.org/10.1007/978-3-540-87407-2_18openalex-snapshot
Defence Responses in Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-00390-5_12openalex-snapshot
Reactive Oxygen Species in Ozone Toxicity
inferred← citeshttps://doi.org/10.1007/978-3-642-00390-5_9openalex-snapshot
Hydrogen Peroxide-Responsive Genes in Stress Acclimation and Cell Death
inferred← citeshttps://doi.org/10.1007/978-3-642-03524-1_12openalex-snapshot
G Proteins and Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-3-642-12162-3_3openalex-snapshot
Plant Defense Signaling from the Underground Primes Aboveground Defenses to Confer Enhanced Resistance in a Cost-Efficient Manner
inferred← citeshttps://doi.org/10.1007/978-3-642-17815-3openalex-snapshot
Recent advances in entomological research : from molecular biology to pest management
inferred← citeshttps://doi.org/10.1007/978-3-642-17815-3_1openalex-snapshot
Deciphering the Plant-Insect Phenotypic Arms Race
inferred← citeshttps://doi.org/10.1007/978-3-642-23524-5_5openalex-snapshot
Jasmonates in Plant Defense Responses
inferred← citeshttps://doi.org/10.1007/978-3-642-36470-9_17openalex-snapshot
Systemic Wound Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-81-322-1542-4_15openalex-snapshot
Recent Trends in Jasmonate Signaling Pathway
inferred← citeshttps://doi.org/10.1007/978-81-322-3706-8_9openalex-snapshot
Plant Responses to Combined Drought and Pathogen Infection: Current Understanding on the Role of Phytohormones
inferred← citeshttps://doi.org/10.1007/978-90-481-2863-1_18openalex-snapshot
Oxidation of Membrane Lipids and Functions of Oxylipins
inferred← citeshttps://doi.org/10.1007/978-90-481-3112-9_10openalex-snapshot
Promoters and Transcription Factors in Abiotic Stress-Responsive Gene Expression
inferred← citeshttps://doi.org/10.1007/978-90-481-3112-9_3openalex-snapshot
Stress Signaling I: The Role of Abscisic Acid (ABA)
inferred← citeshttps://doi.org/10.1007/978-94-007-5724-0_25openalex-snapshot
Photoregulation of Chloroplast Development: Retrograde Signaling
inferred← citeshttps://doi.org/10.1007/978-94-007-7426-1_10openalex-snapshot
Ubiquitin-Proteasome System-Mediated Protein Degradation in Defense Signaling
inferred← citeshttps://doi.org/10.1007/978-94-007-7426-1_7openalex-snapshot
Mitogen-Activated Protein Kinase Cascades in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_3openalex-snapshot
Jasmonate Signaling System in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_5openalex-snapshot
Abscisic Acid Signaling System in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-94-017-9285-1_8openalex-snapshot
Gibberellin Signaling in Plant Innate Immunity
inferred← citeshttps://doi.org/10.1007/978-94-017-9424-4_12openalex-snapshot
Cross Talk of Signaling Pathways Between ABA and Other Phytohormones
inferred← citeshttps://doi.org/10.1007/978-94-017-9424-4_20openalex-snapshot
ABA Regulation of Plant Response to Biotic Stresses
inferred← citeshttps://doi.org/10.1007/978-94-017-9484-8_11openalex-snapshot
Ethylene and Plant Immunity
inferred← citeshttps://doi.org/10.1007/978-94-024-1940-5_4openalex-snapshot
Bioengineering and Molecular Manipulation of Mitogen-Activated Kinases to Activate Plant Innate Immunity for Crop Disease Management
inferred← citeshttps://doi.org/10.1007/978-94-024-1940-5_6openalex-snapshot
Bioengineering and Molecular Manipulation of Jasmonate Signaling System to Activate Plant Immune System for Crop Disease Management
inferred← citeshttps://doi.org/10.1007/978-981-10-2854-0_16openalex-snapshot
Growth Promotion Features of the Maize Microbiome: From an Agriculture Perspective
inferred← citeshttps://doi.org/10.1007/978-981-10-6068-7_9openalex-snapshot
Salicylic Acid: Molecular Basis of Stress Resistance in Plants
inferred← citeshttps://doi.org/10.1007/978-981-15-2467-7_10openalex-snapshot
Role of Phytohormones in Plant Defence Against Insects: Signalling and Crosstalk
inferred← citeshttps://doi.org/10.1007/978-981-15-2467-7_15openalex-snapshot
Microbe-Plant-Insect Interactions: A Comparative Dissection of Interactome
inferred← citeshttps://doi.org/10.1007/978-981-15-7293-7_5openalex-snapshot
How Plants Might Recognize Rhizospheric Bacterial Volatiles
inferred← citeshttps://doi.org/10.1007/978-981-16-0862-9_5openalex-snapshot
Host Resistance Signaling Network System to Multiple Stresses
inferred← citeshttps://doi.org/10.1007/978-981-96-4004-1_12openalex-snapshot
Plant Endophytic Fungi: Communication Mechanism to Deal with Biotic Stress
inferred← citeshttps://doi.org/10.1007/978-981-96-9622-2_9openalex-snapshot
Jasmonic Acid-Mediated Regulation of Plant Biology Under Heavy Metal Stress: Physiological and Molecular Aspects
inferred← citeshttps://doi.org/10.1007/978-981-97-7510-1_15openalex-snapshot
Disease-Resistant Genes and Signal Transduction Pathways and Their Applications in Disease Management
inferred← citeshttps://doi.org/10.1007/bf02637260openalex-snapshot
Biosynthesis and Metabolism of Jasmonates
inferred← citeshttps://doi.org/10.1007/bf02637261openalex-snapshot
Jasmonate-Responsive Gene Expression
inferred← citeshttps://doi.org/10.1007/bf02637262openalex-snapshot
Jasmonates - Signals in Plant-Microbe Interactions
inferred← citeshttps://doi.org/10.1007/bf03030620openalex-snapshot
Signaling pathways for the Biosynthesis and action of Jasmonates
inferred← citeshttps://doi.org/10.1007/bf03036121openalex-snapshot
Host immunity-suppressive molecular weapons of phytopathogenic bacteria
inferred← citeshttps://doi.org/10.1007/s00122-018-3105-7openalex-snapshot
CsMYB36 is involved in the formation of yellow green peel in cucumber (Cucumis sativus L.)
inferred← citeshttps://doi.org/10.1007/s00122-024-04697-8openalex-snapshot
Advances in functional studies of plant MYC transcription factors
inferred← citeshttps://doi.org/10.1007/s00203-017-1354-5openalex-snapshot
Gene expression analyses in tomato near isogenic lines provide evidence for ethylene and abscisic acid biosynthesis fine-tuning during arbuscular mycorrhiza development
inferred← citeshttps://doi.org/10.1007/s00299-007-0375-yopenalex-snapshot
The promoter of the TLC1.1 retrotransposon from Solanum chilense is activated by multiple stress-related signaling molecules
inferred← citeshttps://doi.org/10.1007/s00299-007-0410-zopenalex-snapshot
Identification and characterization of COI1-dependent transcription factor genes involved in JA-mediated response to wounding in Arabidopsis plants
inferred← citeshttps://doi.org/10.1007/s00299-007-0482-9openalex-snapshot
Functional characterization of a cotton late embryogenesis-abundant D113 gene promoter in transgenic tobacco
inferred← citeshttps://doi.org/10.1007/s00299-010-0824-xopenalex-snapshot
Transcriptome analysis of secondary-wall-enriched seed coat tissues of canola (Brassica napus L.)
inferred← citeshttps://doi.org/10.1007/s00299-010-0864-2openalex-snapshot
Transcriptional regulation of the cinnamyl alcohol dehydrogenase gene from sweetpotato in response to plant developmental stage and environmental stress
inferred← citeshttps://doi.org/10.1007/s00299-011-1180-1openalex-snapshot
Beyond gibberellins and abscisic acid: how ethylene and jasmonates control seed germination
inferred← citeshttps://doi.org/10.1007/s00299-011-1188-6openalex-snapshot
Molecular characterization of peach PR genes and their induction kinetics in response to bacterial infection and signaling molecules
inferred← citeshttps://doi.org/10.1007/s00299-012-1381-2openalex-snapshot
Arabidopsis Brassinosteroid-overproducing gulliver3-D/dwarf4-D mutants exhibit altered responses to Jasmonic acid and pathogen
inferred← citeshttps://doi.org/10.1007/s00299-013-1441-2openalex-snapshot
Jasmonate signaling in plant development and defense response to multiple (a)biotic stresses
inferred← citeshttps://doi.org/10.1007/s00299-013-1561-8openalex-snapshot
Wound-induced expression of DEFECTIVE IN ANTHER DEHISCENCE1 and DAD1-like lipase genes is mediated by both CORONATINE INSENSITIVE1-dependent and independent pathways in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-014-1608-5openalex-snapshot
Perception, signaling and cross-talk of jasmonates and the seminal contributions of the Daoxin Xie’s lab and the Chuanyou Li’s lab
inferred← citeshttps://doi.org/10.1007/s00299-014-1724-2openalex-snapshot
The AtLRK10L1.2, Arabidopsis ortholog of wheat LRK10, is involved in ABA-mediated signaling and drought resistance
inferred← citeshttps://doi.org/10.1007/s00299-017-2194-0openalex-snapshot
Transcriptome and phytohormone analysis reveals a comprehensive phytohormone and pathogen defence response in pear self-/cross-pollination
inferred← citeshttps://doi.org/10.1007/s00299-019-02416-yopenalex-snapshot
Co-orthologues of ribosome biogenesis factors in A. thaliana are differentially regulated by transcription factors
inferred← citeshttps://doi.org/10.1007/s00299-019-02450-wopenalex-snapshot
Expression of AoNHX1 increases salt tolerance of rice and Arabidopsis, and bHLH transcription factors regulate AtNHX1 and AtNHX6 in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-019-02490-2openalex-snapshot
ZmMYC2 exhibits diverse functions and enhances JA signaling in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-022-02948-wopenalex-snapshot
Post-translational modifications: emerging regulators manipulating jasmonate biosynthesis and signaling
inferred← citeshttps://doi.org/10.1007/s00299-024-03250-7openalex-snapshot
Comparative transcriptomic analysis of the nodulation-competent zone and inference of transcription regulatory network in silicon applied Glycine max [L.]-Merr. Roots
inferred← citeshttps://doi.org/10.1007/s00299-024-03286-9openalex-snapshot
OPDA/dn-OPDA actions: biosynthesis, metabolism, and signaling
inferred← citeshttps://doi.org/10.1007/s00299-025-03464-3openalex-snapshot
Molecular mechanism of response to low-temperature during the natural overwintering period of Rosa persica
inferred← citeshttps://doi.org/10.1007/s00299-026-03933-3openalex-snapshot
Asparagine Synthetase 1 regulates rice seminal root elongation via jasmonic acid metabolism
inferred← citeshttps://doi.org/10.1007/s00344-007-0012-6openalex-snapshot
Modulation of Plant Defenses by Ethylene
inferred← citeshttps://doi.org/10.1007/s00344-014-9444-yopenalex-snapshot
Arabidopsis Plants Overexpressing the MsDREB2C Exhibit Increased Susceptibility to Alternaria mali Infection
inferred← citeshttps://doi.org/10.1007/s00344-015-9526-5openalex-snapshot
How Jasmonates Earned their Laurels: Past and Present
inferred← citeshttps://doi.org/10.1007/s00344-016-9600-7openalex-snapshot
Plant Defense Signaling and Responses Against Necrotrophic Fungal Pathogens
inferred← citeshttps://doi.org/10.1007/s00344-022-10671-9openalex-snapshot
Genome-Wide Identification, In Silico Characterization of AtCOP1-Targeting Regulatory Proteins Network and their Expression Profiling in The COP1 Downregulated Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00344-022-10881-1openalex-snapshot
Overexpression of CiMYC2 Transcription Factor from Chrysanthemum indicum var. aromaticum Resulted in Modified Trichome Formation and Terpenoid Biosynthesis in Transgenic Tobacco
inferred← citeshttps://doi.org/10.1007/s00344-024-11388-7openalex-snapshot
The Regulation Mechanism of MYC on MeJA-Induced Flavonoids Synthesis in Dendrobium officinale
inferred← citeshttps://doi.org/10.1007/s00344-024-11412-wopenalex-snapshot
Molecular Crosstalk of Jasmonate with Major Phytohormones and Plant Growth Regulators During Diverse Stress Responses
inferred← citeshttps://doi.org/10.1007/s00344-024-11620-4openalex-snapshot
Plant Defense Hormones: Thermoregulation and Their Role in Plant Adaptive Immunity
inferred← citeshttps://doi.org/10.1007/s00425-007-0635-7openalex-snapshot
Identification of the OsOPR7 gene encoding 12-oxophytodienoate reductase involved in the biosynthesis of jasmonic acid in rice
inferred← citeshttps://doi.org/10.1007/s00425-008-0804-3openalex-snapshot
Natural variation in responsiveness of Arabidopsis thaliana to methyl jasmonate is developmentally regulated
inferred← citeshttps://doi.org/10.1007/s00425-009-0890-xopenalex-snapshot
The jasmonate signaling pathway in tomato regulates susceptibility to a toxin-dependent necrotrophic pathogen
inferred← citeshttps://doi.org/10.1007/s00425-010-1143-8openalex-snapshot
Comparative molecular and biochemical characterization of segmentally duplicated 9-lipoxygenase genes ZmLOX4 and ZmLOX5 of maize
inferred← citeshttps://doi.org/10.1007/s00425-012-1705-zopenalex-snapshot
Chemical and genetic exploration of jasmonate biosynthesis and signaling paths
inferred← citeshttps://doi.org/10.1007/s00425-014-2151-xopenalex-snapshot
The phytotoxin coronatine is a multifunctional component of the virulence armament of Pseudomonas syringae
inferred← citeshttps://doi.org/10.1007/s00425-017-2697-5openalex-snapshot
Identification of OsMYC2-regulated senescence-associated genes in rice
inferred← citeshttps://doi.org/10.1007/s00425-017-2701-0openalex-snapshot
Functional characterization of the pinoresinol–lariciresinol reductase-2 gene reveals its roles in yatein biosynthesis and flax defense response
inferred← citeshttps://doi.org/10.1007/s00425-018-3001-zopenalex-snapshot
Transcriptome analysis of root-knot nematode (Meloidogyne incognita)-resistant and susceptible sweetpotato cultivars
inferred← citeshttps://doi.org/10.1007/s00425-019-03100-xopenalex-snapshot
In vitro tissue culture of apple and other Malus species: recent advances and applications
inferred← citeshttps://doi.org/10.1007/s00425-019-03334-9openalex-snapshot
Hydrogen sulfide acts downstream of jasmonic acid to inhibit stomatal development in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-021-03607-2openalex-snapshot
Structural and functional organization of the MYC transcriptional factors in Camellia sinensis
inferred← citeshttps://doi.org/10.1007/s00425-022-03974-4openalex-snapshot
GhMYC2 activates cytochrome P450 gene CYP71BE79 to regulate gossypol biosynthesis in cotton
inferred← citeshttps://doi.org/10.1007/s00425-025-04678-1openalex-snapshot
Genetic responses of plants to urban environmental challenges
inferred← citeshttps://doi.org/10.1007/s00438-009-0481-3openalex-snapshot
Functional characterization of the Arabidopsis bHLH92 transcription factor in abiotic stress
inferred← citeshttps://doi.org/10.1007/s00438-016-1248-2openalex-snapshot
Genome-wide identification and functional analysis of the TIFY gene family in response to drought in cotton
inferred← citeshttps://doi.org/10.1007/s00442-016-3758-3openalex-snapshot
Brevicoryne brassicae aphids interfere with transcriptome responses of Arabidopsis thaliana to feeding by Plutella xylostella caterpillars in a density-dependent manner
inferred← citeshttps://doi.org/10.1007/s00468-010-0447-4openalex-snapshot
Cloning and characterization of HbJAZ1 from the laticifer cells in rubber tree (Hevea brasiliensis Muell. Arg.)
inferred← citeshttps://doi.org/10.1007/s00709-012-0400-zopenalex-snapshot
Stress-induced expression of the transcription factor RERJ1 is tightly regulated in response to jasmonic acid accumulation in rice
inferred← citeshttps://doi.org/10.1007/s00709-016-0960-4openalex-snapshot
The ethylene response factor OsERF109 negatively affects ethylene biosynthesis and drought tolerance in rice
inferred← citeshttps://doi.org/10.1007/s00709-024-01955-wopenalex-snapshot
The wheat pathogenesis-related protein (TdPR1.2) enhanced tolerance to abiotic and biotic stresses in transgenic Arabidopsis plants
inferred← citeshttps://doi.org/10.1007/s10059-010-0009-zopenalex-snapshot
Non-Specific Phytohormonal Induction of AtMYB44 and Suppression of Jasmonate-Responsive Gene Activation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10142-013-0309-4openalex-snapshot
Wheat resistome in response to barley yellow dwarf virus infection
inferred← citeshttps://doi.org/10.1007/s10142-015-0468-6openalex-snapshot
Jasmonic acid involves in grape fruit ripening and resistant against Botrytis cinerea
inferred← citeshttps://doi.org/10.1007/s10142-018-0644-6openalex-snapshot
Transcriptome-based mining and expression profiling of Pythium responsive transcription factors in Zingiber sp.
inferred← citeshttps://doi.org/10.1007/s10142-023-01203-zopenalex-snapshot
Identification and characterization of TMV-induced volatile signals in Nicotiana benthamiana: evidence for JA/ET defense pathway priming in congeneric neighbors via airborne (E)-2-octenal
inferred← citeshttps://doi.org/10.1007/s10265-006-0279-xopenalex-snapshot
Influx of extracellular Ca2+ involved in jasmonic-acid-induced elevation of [Ca2+]cyt and JR1 expression in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10265-011-0412-3openalex-snapshot
ABA-mediated transcriptional regulation in response to osmotic stress in plants
inferred← citeshttps://doi.org/10.1007/s10265-012-0509-3openalex-snapshot
Inhibition of arabidopsis hypocotyl elongation by jasmonates is enhanced under red light in phytochrome B dependent manner
inferred← citeshttps://doi.org/10.1007/s10327-018-0799-yopenalex-snapshot
Nonhost resistance of Arabidopsis thaliana against Colletotrichum species
inferred← citeshttps://doi.org/10.1007/s10327-019-00855-9openalex-snapshot
Nicotiana benthamiana exportin 1 is required for elicitor-induced phytoalexin production, cell death induction, and resistance against potato late blight pathogen Phytophthora infestans
inferred← citeshttps://doi.org/10.1007/s10526-013-9554-7openalex-snapshot
Trichoderma atroviride LU132 promotes plant growth but not induced systemic resistance to Plutella xylostella in oilseed rape
inferred← citeshttps://doi.org/10.1007/s10529-014-1549-7openalex-snapshot
Identification of soybean MYC2-like transcription factors and overexpression of GmMYC1 could stimulate defense mechanism against common cutworm in transgenic tobacco
inferred← citeshttps://doi.org/10.1007/s10658-018-1427-6openalex-snapshot
Genome-wide gene expression profiles in response to downy mildew in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
inferred← citeshttps://doi.org/10.1007/s10681-026-03730-9openalex-snapshot
Identification of both shared and isolate-specific QTL and underlying candidate genes for Vanilla planifolia resistance to Fusarium root and stem rot
inferred← citeshttps://doi.org/10.1007/s10725-008-9317-0openalex-snapshot
Is there crosstalk between extracellular and intracellular calcium mobilization in jasmonic acid signaling
inferred← citeshttps://doi.org/10.1007/s10725-019-00512-3openalex-snapshot
Knockdown of SlNL33 accumulates ascorbate, enhances disease and oxidative stress tolerance in tomato (Solanum lycopersicum)
inferred← citeshttps://doi.org/10.1007/s10725-019-00555-6openalex-snapshot
Coronatine inhibits mesocotyl elongation by promoting ethylene production in etiolated maize seedlings
inferred← citeshttps://doi.org/10.1007/s10725-022-00946-2openalex-snapshot
ZmTIFY16, a novel maize TIFY transcription factor gene, promotes root growth and development and enhances drought and salt tolerance in Arabidopsis and Zea mays
inferred← citeshttps://doi.org/10.1007/s10725-026-01456-1openalex-snapshot
Brassinosteroids and jasmonic acid signaling: a molecular roadmap to abiotic stress resilience in crops
inferred← citeshttps://doi.org/10.1007/s10886-014-0474-5openalex-snapshot
The Evolution of Ethylene Signaling in Plant Chemical Ecology
inferred← citeshttps://doi.org/10.1007/s11032-014-0118-zopenalex-snapshot
Quantitative analysis of race-specific resistance to Colletotrichum lindemuthianum in common bean
inferred← citeshttps://doi.org/10.1007/s11032-020-01113-zopenalex-snapshot
Overexpression of a TIFY family gene, GsJAZ2, exhibits enhanced tolerance to alkaline stress in soybean
inferred← citeshttps://doi.org/10.1007/s11033-012-1542-yopenalex-snapshot
Identification and expression of C2H2 transcription factor genes in Carica papaya under abiotic and biotic stresses
inferred← citeshttps://doi.org/10.1007/s11101-006-9051-zopenalex-snapshot
Transcription factors involved in terpenoid indole alkaloid biosynthesis in Catharanthus roseus
inferred← citeshttps://doi.org/10.1007/s11101-016-9468-yopenalex-snapshot
Discovery and metabolic engineering of iridoid/secoiridoid and monoterpenoid indole alkaloid biosynthesis
inferred← citeshttps://doi.org/10.1007/s11101-017-9510-8openalex-snapshot
Metabolism of the plant hormone jasmonate: a sentinel for tissue damage and master regulator of stress response
inferred← citeshttps://doi.org/10.1007/s11103-005-7294-5openalex-snapshot
Arabidopsis ERF4 is a transcriptional repressor capable of modulating ethylene and abscisic acid responses
inferred← citeshttps://doi.org/10.1007/s11103-005-7306-5openalex-snapshot
Expression profiling reveals COI1 to be a key regulator of genes involved in wound- and methyl jasmonate-induced secondary metabolism, defence, and hormone interactions
inferred← citeshttps://doi.org/10.1007/s11103-007-9204-5openalex-snapshot
The HvNAC6 transcription factor: a positive regulator of penetration resistance in barley and Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-007-9230-3openalex-snapshot
The bHLH-type transcription factor AtAIB positively regulates ABA response in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-008-9435-0openalex-snapshot
Role of plant hormones in plant defence responses
inferred← citeshttps://doi.org/10.1007/s11103-009-9524-8openalex-snapshot
Identification and expression profiling analysis of TIFY family genes involved in stress and phytohormone responses in rice
inferred← citeshttps://doi.org/10.1007/s11103-010-9728-yopenalex-snapshot
Two GCC boxes and AP2/ERF-domain transcription factor ORA59 in jasmonate/ethylene-mediated activation of the PDF1.2 promoter in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-016-0480-9openalex-snapshot
Jasmonates: signal transduction components and their roles in environmental stress responses
inferred← citeshttps://doi.org/10.1007/s11103-016-0481-8openalex-snapshot
How plants handle multiple stresses: hormonal interactions underlying responses to abiotic stress and insect herbivory
inferred← citeshttps://doi.org/10.1007/s11103-016-0503-6openalex-snapshot
Physiological impacts of ABA–JA interactions under water-limitation
inferred← citeshttps://doi.org/10.1007/s11103-020-01005-yopenalex-snapshot
Transcriptional and metabolite analysis reveal a shift in direct and indirect defences in response to spider-mite infestation in cucumber (Cucumis sativus)
inferred← citeshttps://doi.org/10.1007/s11103-020-01009-8openalex-snapshot
Correction to: Transcriptional and metabolite analysis reveal a shift in direct and indirect defences in response to spider‑mite infestation in cucumber (Cucumis sativus)
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/10.1007/s11103-021-01186-0openalex-snapshot
The rice wound-inducible transcription factor RERJ1 sharing same signal transduction pathway with OsMYC2 is necessary for defense response to herbivory and bacterial blight
inferred← citeshttps://doi.org/10.1007/s11103-023-01411-yopenalex-snapshot
The N-terminal α2 helix element is critical for the activity of the rice transcription factor MYC2
inferred← citeshttps://doi.org/10.1007/s11104-024-06741-4openalex-snapshot
Gluconacetobacter diazotrophicus triggers ISR involving SA and JA/Et defense-related pathways to respond against Ralstonia solanacearum in Arabidopsis and optimizes the cellular redox state maintaining reduced FITNESS levels
inferred← citeshttps://doi.org/10.1007/s11105-009-0112-5openalex-snapshot
Molecular Cloning and Characterization of a Novel Gossypium hirsutum L. bHLH Gene in Response to ABA and Drought Stresses
inferred← citeshttps://doi.org/10.1007/s11105-013-0645-5openalex-snapshot
Defence Signalling Pathways Involved in Plant Resistance and Phosphite-Mediated Control of Phytophthora Cinnamomi
inferred← citeshttps://doi.org/10.1007/s11105-014-0822-1openalex-snapshot
Molecular Insights into Plant-Phytopathogenic Bacteria Interactions
inferred← citeshttps://doi.org/10.1007/s11105-016-0993-zopenalex-snapshot
Differential Impact of Acclimation and Acute Water Deprivation in the Expression of Key Transcription Factors in Soybean Roots
inferred← citeshttps://doi.org/10.1007/s11105-021-01280-zopenalex-snapshot
Allantoin: Emerging Role in Plant Abiotic Stress Tolerance
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