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Jasmonic acid is a crucial signal transducer in heat shock induced sesquiterpene formation in Aquilaria sinensis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470988800.ch7openalex-snapshot
Oxylipins: Biosynthesis, Signal Transduction and Action
inferredcites →https://doi.org/10.1002/9781119312994.apr0248openalex-snapshot
Oxylipins: Biosynthesis, Signal Transduction and Action
inferredcites →https://doi.org/10.1002/bit.21122openalex-snapshot
The effect of heat shock on paclitaxel production in Taxus yunnanensis cell suspension cultures: Role of abscisic acid pretreatment
inferredcites →https://doi.org/10.1002/cbdv.201100077openalex-snapshot
Chemical Constituents of Agarwood Originating from the Endemic Genus Aquilaria Plants
inferredcites →https://doi.org/10.1002/pca.1085openalex-snapshot
Study on the extraction, purification and quantification of jasmonic acid, abscisic acid and indole‐3‐acetic acid in plants
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/978-1-4020-8261-0_12openalex-snapshot
Growing ‘The Wood of The Gods’: Agarwood Production in Southeast Asia
inferredcites →https://doi.org/10.1007/bf02637263openalex-snapshot
Jasmonates as Signals in the Wound Response
inferredcites →https://doi.org/10.1007/s00299-012-1289-xopenalex-snapshot
Selection and validation of reference genes for studying stress-related agarwood formation of Aquilaria sinensis
inferredcites →https://doi.org/10.1007/s004250000316openalex-snapshot
Transgenic Nicotiana tabacum and Arabidopsis thaliana plants overexpressing allene oxide synthase
inferredcites →https://doi.org/10.1007/s10725-013-9838-zopenalex-snapshot
Hydrogen peroxide induces vessel occlusions and stimulates sesquiterpenes accumulation in stems of Aquilaria sinensis
inferredcites →https://doi.org/10.1016/j.biotechadv.2005.01.003openalex-snapshot
Elicitor signal transduction leading to production of plant secondary metabolites
inferredcites →https://doi.org/10.1016/j.chembiol.2006.01.009openalex-snapshot
Involvement of Reactive Oxygen Species and Reactive Nitrogen Species in the Wound Response of Dasycladus vermicularis
inferredcites →https://doi.org/10.1016/j.pbi.2005.05.008openalex-snapshot
Systemic signaling in the wound response
inferredcites →https://doi.org/10.1016/j.phytochem.2007.04.008openalex-snapshot
The rice (E)-β-caryophyllene synthase (OsTPS3) accounts for the major inducible volatile sesquiterpenes
inferredcites →https://doi.org/10.1016/j.phytochem.2009.07.032openalex-snapshot
Enzymes in jasmonate biosynthesis – Structure, function, regulation
inferredcites →https://doi.org/10.1016/j.phytochem.2009.08.004openalex-snapshot
The power of mutants for investigating jasmonate biosynthesis and signaling
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.007openalex-snapshot
ROS signaling: the new wave?
inferredcites →https://doi.org/10.1016/s1369-5266(02)00275-3openalex-snapshot
Cross talk between signaling pathways in pathogen defense
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/10.1023/a:1023049319723openalex-snapshot
Jasmonate biosynthesis and the allene oxide cyclase family of Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00861.xopenalex-snapshot
Tissue‐specific oxylipin signature of tomato flowers: allene oxide cyclase is highly expressed in distinct flower organs and vascular bundles
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01328.xopenalex-snapshot
A knock‐out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01647.xopenalex-snapshot
Allene oxide cyclase dependence of the wound response and vascular bundle‐specific generation of jasmonates in tomato – amplification in wound signalling
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01921.xopenalex-snapshot
Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth‐related transcriptional reorganization in Nicotiana attenuata
inferredcites →https://doi.org/10.1055/s-2005-837634openalex-snapshot
The tu8 Mutation of Arabidopsis thaliana Encoding a Heterochromatin Protein 1 Homolog Causes Defects in the Induction of Secondary Metabolite Biosynthesis
inferredcites →https://doi.org/10.1071/fp14189openalex-snapshot
Hydrogen peroxide promotes programmed cell death and salicylic acid accumulation during the induced production of sesquiterpenes in cultured cell suspensions of Aquilaria sinensis
inferredcites →https://doi.org/10.1073/pnas.89.6.2389openalex-snapshot
Jasmonic acid is a signal transducer in elicitor-induced plant cell cultures.
inferredcites →https://doi.org/10.1073/pnas.94.10.5473openalex-snapshot
Jasmonate is essential for insect defense in Arabidopsis
inferredcites →https://doi.org/10.1080/10412905.2005.9698867openalex-snapshot
Induction of Sesquiterpenoid Production by Methyl Jasmonate in Aquilaria sinensis Cell Suspension Culture
inferredcites →https://doi.org/10.1093/aob/mcm079openalex-snapshot
Jasmonates: An Update on Biosynthesis, Signal Transduction and Action in Plant Stress Response, Growth and Development
inferredcites →https://doi.org/10.1093/pcp/pcg072openalex-snapshot
Enzymes of Jasmonate Biosynthesis Occur in Tomato Sieve Elements
inferredcites →https://doi.org/10.1093/pcp/pcr063openalex-snapshot
Tobacco MYC2 Regulates Jasmonate-Inducible Nicotine Biosynthesis Genes Directly and By Way of the NIC2-Locus ERF Genes
inferredcites →https://doi.org/10.1101/gad.297704openalex-snapshot
Conserved MYC transcription factors play a key role in jasmonate signaling both in tomato and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.100.1.433openalex-snapshot
Expression, Activity, and Cellular Accumulation of Methyl Jasmonate-Responsive Lipoxygenase in Soybean Seedlings
inferredcites →https://doi.org/10.1104/pp.107.108902openalex-snapshot
Involvement of Polyamine Oxidase in Wound Healing
inferredcites →https://doi.org/10.1104/pp.107.112029openalex-snapshot
Cross Talk in Defense Signaling
inferredcites →https://doi.org/10.1104/pp.107.115717openalex-snapshot
Jasmonate Signaling: Toward an Integrated View
inferredcites →https://doi.org/10.1104/pp.110.161828openalex-snapshot
Characterization of δ-Guaiene Synthases from Cultured Cells of Aquilaria , Responsible for the Formation of the Sesquiterpenes in Agarwood
inferredcites →https://doi.org/10.1104/pp.110.2.387openalex-snapshot
Involvement of Jasmonic Acid in Elicitor-Induced Phytoalexin Production in Suspension-Cultured Rice Cells
inferredcites →https://doi.org/10.1104/pp.111.181834openalex-snapshot
The Transcription Factor CrWRKY1 Positively Regulates the Terpenoid Indole Alkaloid Biosynthesis in Catharanthus roseus
inferredcites →https://doi.org/10.1104/pp.122.4.1335openalex-snapshot
Expression of Allene Oxide Synthase Determines Defense Gene Activation in Tomato
inferredcites →https://doi.org/10.1104/pp.123.2.711openalex-snapshot
Cytochrome P450-Dependent Metabolism of Oxylipins in Tomato. Cloning and Expression of Allene Oxide Synthase and Fatty Acid Hydroperoxide Lyase
inferredcites →https://doi.org/10.1104/pp.72.3.817openalex-snapshot
Heat Stress Responses in Cultured Plant Cells
inferredcites →https://doi.org/10.1104/pp.74.4.944openalex-snapshot
Heat Stress Responses in Cultured Plant Cells
inferredcites →https://doi.org/10.1105/tpc.022319openalex-snapshot
JASMONATE-INSENSITIVE1 Encodes a MYC Transcription Factor Essential to Discriminate between Different Jasmonate-Regulated Defense Responses in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.106.048017openalex-snapshot
MYC2 Differentially Modulates Diverse Jasmonate-Dependent Functions in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.098749openalex-snapshot
Arabidopsis MYC2 Interacts with DELLA Proteins in Regulating Sesquiterpene Synthase Gene Expression
inferredcites →https://doi.org/10.1105/tpc.114.133181openalex-snapshot
Virulence Factors of Geminivirus Interact with MYC2 to Subvert Plant Resistance and Promote Vector Performance
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04575.xopenalex-snapshot
The basic helix‐loop‐helix transcription factor CrMYC2 controls the jasmonate‐responsive expression of the ORCA genes that regulate alkaloid biosynthesis in Catharanthus roseus
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03466.xopenalex-snapshot
Dissection of the phytohormonal regulation of trichome formation and biosynthesis of the antimalarial compound artemisinin in Artemisia annua plants
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103854openalex-snapshot
Plant Defense Against Herbivores: Chemical Aspects
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154055openalex-snapshot
Hormonal Modulation of Plant Immunity
inferredcites →https://doi.org/10.1146/annurev.arplant.043008.092007openalex-snapshot
Jasmonate Passes Muster: A Receptor and Targets for the Defense Hormone
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092825openalex-snapshot
Plant Immunity to Insect Herbivores
inferredcites →https://doi.org/10.1186/1471-2164-14-227openalex-snapshot
Identification of genes related to agarwood formation: transcriptome analysis of healthy and wounded tissues of Aquilaria sinensis
inferredcites →https://doi.org/10.1186/1471-2164-9-432openalex-snapshot
Heat stress-responsive transcriptome analysis in heat susceptible and tolerant wheat (Triticum aestivum L.) by using Wheat Genome Array
inferredcites →https://doi.org/10.1186/1471-2229-12-128openalex-snapshot
Jasmonic acid is involved in the signaling pathway for fungal endophyte-induced volatile oil accumulation of Atractylodes lancea plantlets
inferredcites →https://doi.org/10.1186/1472-6882-10-68openalex-snapshot
Laxative effects of agarwood on low-fiber diet-induced constipation in rats
inferredcites →https://doi.org/10.17660/actahortic.2005.676.20openalex-snapshot
MECHANICAL METHODS TO STIMULATE ALOES WOOD FORMATION IN AQUILARIA CRASSNA PIERRE EX H.LEC. (KRITSANA) TREES
inferredcites →https://doi.org/10.3390/molecules16064884openalex-snapshot
Comparison of Compositions and Antimicrobial Activities of Essential Oils from Chemically Stimulated Agarwood, Wild Agarwood and Healthy Aquilaria sinensis (Lour.) Gilg Trees
inferredcites →https://doi.org/10.3390/molecules18033086openalex-snapshot
Whole-tree Agarwood-Inducing Technique: An Efficient Novel Technique for Producing High-Quality Agarwood in Cultivated Aquilaria sinensis Trees
inferredcites →https://doi.org/10.5402/2012/243694openalex-snapshot
Understanding Heat Stress Tolerance of Suspended Cells in the Model Plant Populus euphratica
inferredcites →https://doi.org/10.5511/plantbiotechnology.26.307openalex-snapshot
Production of agarwood fragrant constituents in Aquilaria calli and cell suspension cultures
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/mycokeys.112.139831zenodo-depositor-declared
New Aquilariomyces and Mangifericomes species (Pleosporales, Ascomycota) from Aquilaria spp. in China
inferred← citeshttps://doi.org/10.1002/9781119468677.ch1openalex-snapshot
Regulated Suicide for Survival
inferred← citeshttps://doi.org/10.1002/jemt.24140openalex-snapshot
Programmed cell death might involve in progress of wounding induced agarwood formation in stems of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1002/pmic.201800023openalex-snapshot
iTRAQ‐Based Quantitative Proteomic Analysis of Chemically Induced Aquilaria sinensis Provides Insights into Agarwood Formation Mechanism
inferred← citeshttps://doi.org/10.1002/ppp3.10457openalex-snapshot
Plant nutritional value of aquaculture water produced by feeding Nile tilapia ( Oreochromis niloticus ) alternative protein diets: A lettuce and basil case study
inferred← citeshttps://doi.org/10.1002/ps.5540openalex-snapshot
Production of pyrrolizidine alkaloids and shikonins in Echium plantagineum L. in response to various plant stressors
inferred← citeshttps://doi.org/10.1007/978-3-030-03589-1_10openalex-snapshot
Endophytic Fungi: The Desired Biostimulants for Essential Oil Production
inferred← citeshttps://doi.org/10.1007/978-3-030-65912-7_19openalex-snapshot
Medicinal Plants and Their Pharmaceutical Properties Under Adverse Environmental Conditions
inferred← citeshttps://doi.org/10.1007/978-3-030-65912-7_7openalex-snapshot
Molecular Mechanisms of Heat Shock Proteins for Sustainable Plant Growth and Production
inferred← citeshttps://doi.org/10.1007/978-3-319-68717-9_4openalex-snapshot
Metabolic Responses of Medicinal Plants to Global Warming, Temperature and Heat Stress
inferred← citeshttps://doi.org/10.1007/978-94-017-7758-2_1openalex-snapshot
Role of Hormones in Plant Adaptation to Heat Stress
inferred← citeshttps://doi.org/10.1007/s00299-020-02614-zopenalex-snapshot
Jasmonic acid: a key frontier in conferring abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1007/s00344-026-12313-wopenalex-snapshot
Elicitors in Plant Defense: Exploring Their Role in Biotic and Abiotic Stress Resistance
inferred← citeshttps://doi.org/10.1007/s00468-018-1799-4openalex-snapshot
Interxylary phloem and xylem rays are the structural foundation of agarwood resin formation in the stems of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1007/s00468-021-02180-1openalex-snapshot
Transcript profiling leads to biomarker identification for agarwood resin-loaded Aquilaria malaccensis
inferred← citeshttps://doi.org/10.1007/s00468-025-02703-0openalex-snapshot
The xylem anatomical structure, physiological characteristics and aromatic components analyses explain the difference of fungal solution induced agarwood formation in Aquilaria sinensis
inferred← citeshttps://doi.org/10.1007/s00468-026-02803-5openalex-snapshot
Calcium-dependent protein kinase (CDPK) gene family in Aquilaria agallocha tree: genome-wide identification and expression analysis under stress conditions
inferred← citeshttps://doi.org/10.1007/s11103-017-0588-6openalex-snapshot
Isolation and functional characterization of a methyl jasmonate-responsive 3-carene synthase from Lavandula x intermedia
inferred← citeshttps://doi.org/10.1007/s11676-022-01542-wopenalex-snapshot
Identification of sesquiterpene synthase genes in the genome of Aquilaria sinensis and characterization of an α-humulene synthase
inferred← citeshttps://doi.org/10.1007/s11816-022-00758-wopenalex-snapshot
AsJAZ1 represses the expression of the sesquiterpene synthase gene based on the JA signaling pathway in Aquilaria sinensis (Lour.) Gilg
inferred← citeshttps://doi.org/10.1007/s12298-021-01040-zopenalex-snapshot
Genome-wide detection and classification of terpene synthase genes in Aquilaria agallochum
inferred← citeshttps://doi.org/10.1007/s13199-020-00677-wopenalex-snapshot
Fusarium solani induces the formation of agarwood in Gyrinops versteegii (Gilg.) Domke branches
inferred← citeshttps://doi.org/10.1007/s44372-024-00020-3openalex-snapshot
Plant development and heat stress: role of exogenous nutrients and phytohormones in thermotolerance
inferred← citeshttps://doi.org/10.1007/s44372-025-00308-yopenalex-snapshot
Chemical induction for agarwood formation: a recent review
inferred← citeshttps://doi.org/10.1016/b978-0-12-816483-9.00008-6openalex-snapshot
Medicinal Plants Under Climate Change: Impacts on Pharmaceutical Properties of Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-817562-0.00006-9openalex-snapshot
Effect of High-Temperature Stress on the Metabolism of Plant Growth Regulators
inferred← citeshttps://doi.org/10.1016/b978-0-323-91005-7.00020-5openalex-snapshot
Jasmonates: key players in plant stress tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-323-91886-2.00010-0openalex-snapshot
Understanding the role of phytohormones in governing heat, cold, and freezing stress response
inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.104435openalex-snapshot
Biodiversity and application prospects of fungal endophytes in the agarwood-producing genera, Aquilaria and Gyrinops (Thymelaeaceae): A review
inferred← citeshttps://doi.org/10.1016/j.cub.2020.01.023openalex-snapshot
An Ancient COI1-Independent Function for Reactive Electrophilic Oxylipins in Thermotolerance
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104551openalex-snapshot
Phloem-feeding insect infestation antagonizes volatile organic compound emissions and enhances heat stress recovery of photosynthesis in Origanum vulgare
inferred← citeshttps://doi.org/10.1016/j.fbio.2024.105535openalex-snapshot
The fungal strain promotes rapid agarwood resin production with medicinally accepted agarotetrol level
inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e06725openalex-snapshot
Methyl jasmonate and crude extracts of Fusarium solani elicit agarwood compounds in shoot culture of Aquilaria malaccensis Lamk.
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.123758openalex-snapshot
Genome-wide investigation of Cytochrome P450 superfamily of Aquilaria agallocha: Association with terpenoids and phenylpropanoids biosynthesis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115263openalex-snapshot
Three candidate 2-(2-phenylethyl)chromone-producing type III polyketide synthases from Aquilaria sinensis (Lour.) Gilg have multifunctions synthesizing benzalacetones, quinolones and pyrones
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115908openalex-snapshot
E3 ubiquitin ligase RING3 mediates AsWRKY44 degradation to promote wound-induced sesquiterpene biosynthesis in Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119227openalex-snapshot
Exploring the role of jasmonic acid in boosting the production of secondary metabolites in medicinal plants: Pathway for future research
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.02.006openalex-snapshot
Hydrogen peroxide burst triggers accumulation of jasmonates and salicylic acid inducing sesquiterpene biosynthesis in wounded Aquilaria sinesis
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.152994openalex-snapshot
Methyl jasmonate-induced compositional changes of volatile organic compounds in Polygonum minus leaves
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.01.002openalex-snapshot
H2O2 and NADPH oxidases involve in regulation of 2-(2-phenylethyl)chromones accumulation during salt stress in Aquilaria sinensis calli
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112477openalex-snapshot
Role of jasmonates in plant response to temperature stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.04.028openalex-snapshot
Genome-wide identification and expression analysis of terpene synthase gene family in Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108238openalex-snapshot
Plant hormones and secondary metabolites under environmental stresses: Enlightening defense molecules
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110260openalex-snapshot
Coordinated regulation between jasmonic acid and abscisic acid mediates drought tolerance in sweetpotato
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102806openalex-snapshot
Integrative pathophysiology of agarwood formation: from fungal entry to metabolite accumulation
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2023.112326openalex-snapshot
Nordihydroguaiaretic acid (NDGA) maintains the postharvest quality of fresh daylily flower buds (Hemerocallis citrina) by enhancing antioxidant metabolism and regulating phytohormone equilibrium
inferred← citeshttps://doi.org/10.1016/j.rse.2025.114884openalex-snapshot
Metabolite-derived spectral modelling can differentiate heat and drought stress under hot-dry environments
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.01.021openalex-snapshot
Karrikins-induced accumulation of Salvianolic acid B is regulated by Jasmonic acid and hydrogen peroxide in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1016/j.scienta.2017.03.004openalex-snapshot
Effect of methyl jasmonic acid on peach fruit ripening progress
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101013openalex-snapshot
Heat tolerance in Arabidopsis thaliana seedlings requires functional DMS3, a component of de novo methylation
inferred← citeshttps://doi.org/10.1016/j.tplants.2023.11.008openalex-snapshot
Plant secondary metabolism in a fluctuating world: climate change perspectives
inferred← citeshttps://doi.org/10.1038/s41598-020-59597-wopenalex-snapshot
Genome-wide analysis of WRKY transcription factors in Aquilaria sinensis (Lour.) Gilg
inferred← citeshttps://doi.org/10.1038/s41598-022-10785-wopenalex-snapshot
Genome-wide analysis of basic helix–loop–helix (bHLH) transcription factors in Aquilaria sinensis
inferred← citeshttps://doi.org/10.1038/s41598-025-04230-xopenalex-snapshot
Optimization and induction effect evaluation of complex inducer of Aquilaria sinensis based on factorial design
inferred← citeshttps://doi.org/10.1038/srep44406openalex-snapshot
Chemometric analysis reveals links in the formation of fragrant bio-molecules during agarwood (Aquilaria malaccensis) and fungal interactions
inferred← citeshttps://doi.org/10.1039/c8ra10616aopenalex-snapshot
Time-based LC-MS/MS analysis provides insights into early responses to mechanical wounding, a major trigger to agarwood formation in Aquilaria malaccensis Lam
inferred← citeshttps://doi.org/10.1039/d0np00042fopenalex-snapshot
Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesis
inferred← citeshttps://doi.org/10.1080/01904167.2020.1799004openalex-snapshot
Current scenario and future prospects of plant growth-promoting rhizobacteria: an economic valuable resource for the agriculture revival under stressful conditions
inferred← citeshttps://doi.org/10.1093/jxb/erab257openalex-snapshot
Temperature regulation of plant hormone signaling during stress and development
inferred← citeshttps://doi.org/10.1093/jxb/erz469openalex-snapshot
AsWRKY44 represses the wound-induced sesquiterpene biosynthetic gene ASS1 expression in Aquilaria sinensis (Lour.) Gilg
inferred← citeshttps://doi.org/10.1093/pcp/pcx122openalex-snapshot
Transcription Factor AsMYC2 Controls the Jasmonate-Responsive Expression of ASS1 Regulating Sesquiterpene Biosynthesis in Aquilaria sinensis (Lour.) Gilg
inferred← citeshttps://doi.org/10.1093/plphys/kiac220openalex-snapshot
MEDIATOR SUBUNIT17 integrates jasmonate and auxin signaling pathways to regulate thermomorphogenesis
inferred← citeshttps://doi.org/10.1093/treephys/tpae023openalex-snapshot
Stem heating results in hydraulic dysfunction in Symplocos tinctoria: implications for post-fire tree death
inferred← citeshttps://doi.org/10.1101/2023.05.08.539809openalex-snapshot
Genome-wide analysis of Respiratory burst oxidase homolog ( Rboh ) genes in Aquilaria species and its association with agarwood formation
inferred← citeshttps://doi.org/10.1101/2025.04.27.650281openalex-snapshot
Genome-wide identification and expression analysis of CDPK proteins in agarwood-producing Aquilaria agallocha trees
inferred← citeshttps://doi.org/10.1111/jse.13128openalex-snapshot
The polyphasic approach reveals ten novel and one known Ascomycota taxa from terrestrial agarwood‐producing trees
inferred← citeshttps://doi.org/10.1111/ppl.13247openalex-snapshot
Exogenous abscisic acid and jasmonic acid restrain polyethylene glycol‐induced drought by improving the growth and antioxidative enzyme activities in pearl millet
inferred← citeshttps://doi.org/10.1111/ppl.70923openalex-snapshot
The Evolutionarily Conserved Jasmonate Pathway Positively Affects Desiccation Tolerance on Syntrichia caninervis by Boosting Antioxidant Capacity
inferred← citeshttps://doi.org/10.1134/s0003683821010117openalex-snapshot
Jasmonate Signaling and Plant Adaptation to Abiotic Stressors (Review)
inferred← citeshttps://doi.org/10.1134/s1021443722601586openalex-snapshot
Physiological Response of Avena sativa to Low-Temperature Stress is Promoted by Bacillus amyloliquefaciens GL18 and Its Functional Genes
inferred← citeshttps://doi.org/10.1139/gen-2022-0003openalex-snapshot
Genome-wide investigation and expression analysis of the AP2/ERF family for selection of agarwood-related genes in Aquilaria sinensis (Lour.) Gilg
inferred← citeshttps://doi.org/10.1186/s12870-022-03821-4openalex-snapshot
Comparative transcriptome analysis reveals different defence responses during the early stage of wounding stress in Chi-Nan germplasm and ordinary Aquilaria sinensis
inferred← citeshttps://doi.org/10.1360/ssv-2023-0291openalex-snapshot
Advancements in agarwood germplasm resources, quality evaluation, and formation mechanism
inferred← citeshttps://doi.org/10.1371/journal.pone.0227608openalex-snapshot
Interaction between elevated temperature and different types of Na-salicylate treatment in Brachypodium dystachion
inferred← citeshttps://doi.org/10.1371/journal.pone.0327516openalex-snapshot
An efficient harvesting strategy for agarwood based on the correlation analysis of resin formation and leaves dynamic changes induced by integrated induction method
inferred← citeshttps://doi.org/10.17221/45/2025-cjgpbopenalex-snapshot
Transcriptome analysis reveals differential gene expression in tomato under high-temperature stress
inferred← citeshttps://doi.org/10.30848/pjb2019-5(16)openalex-snapshot
Experimental induction of 2-(2-phenylethyl) Chromone in aerial roots of Aquilaria sinensis
inferred← citeshttps://doi.org/10.32615/bp.2020.141openalex-snapshot
Cloning and functional analysis of the promoterof the sesquiterpene synthase gene ASS1 in Aquilaria sinensis
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1446583openalex-snapshot
Aromatic components and endophytic fungi during the formation of agarwood in Aquilaria sinensis were induced by exogenous substances
inferred← citeshttps://doi.org/10.3389/fphar.2024.1468393openalex-snapshot
Pharmacology and therapeutic potential of agarwood and agarwood tree leaves in periodontitis
inferred← citeshttps://doi.org/10.3389/fpls.2018.00819openalex-snapshot
Combined Drought and Heat Activates Protective Responses in Eucalyptus globulus That Are Not Activated When Subjected to Drought or Heat Stress Alone
inferred← citeshttps://doi.org/10.3389/fpls.2019.00122openalex-snapshot
Agarwood Induction: Current Developments and Future Perspectives
inferred← citeshttps://doi.org/10.3389/fpls.2019.00840openalex-snapshot
The Scent of Stress: Evidence From the Unique Fragrance of Agarwood
inferred← citeshttps://doi.org/10.3389/fpls.2023.1281877openalex-snapshot
Effects of ethephon on heartwood formation and related physiological indices of Dalbergia odorifera T. Chen
inferred← citeshttps://doi.org/10.3389/fpls.2023.1326080openalex-snapshot
Genome-wide analysis of respiratory burst oxidase homolog (Rboh) genes in Aquilaria species and insight into ROS-mediated metabolites biosynthesis and resin deposition
inferred← citeshttps://doi.org/10.3389/fpls.2024.1437105openalex-snapshot
2-(2-Phenylethyl)chromones increase in Aquilaria sinensis with the formation of agarwood
inferred← citeshttps://doi.org/10.3389/fpls.2024.1461048openalex-snapshot
Physiological characteristics during the formation of aromatic components in xylem of Aquilaria sinensis induced by exogenous substances
inferred← citeshttps://doi.org/10.3389/fpls.2025.1587337openalex-snapshot
Medicinal plants in a changing climate: understanding the links between environmental stress and secondary metabolite synthesis
inferred← citeshttps://doi.org/10.3389/fpls.2025.1664465openalex-snapshot
MsDAD1 acts as a heat-induced “senescence brake” in alfalfa
inferred← citeshttps://doi.org/10.3389/fpls.2026.1750077openalex-snapshot
Dynamic regulation of secondary metabolites and agarwood aroma compounds in Aquilaria sinensis by the endophytic fungus NSZJ-CX-22 revealed through metabolomics and GC–MS
inferred← citeshttps://doi.org/10.3390/agriculture15181950openalex-snapshot
Environmental Effects on Atractylodes macrocephala Rhizome Growth and Compounds
inferred← citeshttps://doi.org/10.3390/d14030211openalex-snapshot
Diversity and Biosynthetic Activities of Agarwood Associated Fungi
inferred← citeshttps://doi.org/10.3390/genes10090683openalex-snapshot
Transcript Abundance Patterns of 9- and 13-Lipoxygenase Subfamily Gene Members in Response to Abiotic Stresses (Heat, Cold, Drought or Salt) in Tomato (Solanum lycopersicum L.) Highlights Member-Specific Dynamics Relevant to Each Stress
inferred← citeshttps://doi.org/10.3390/genes13010008openalex-snapshot
Genome-Wide Identification and Characterization of HSP70 Gene Family in Aquilaria sinensis (Lour.) Gilg
inferred← citeshttps://doi.org/10.3390/ijms20102479openalex-snapshot
Jasmonic Acid Signaling Pathway in Plants
inferred← citeshttps://doi.org/10.3390/ijms21218052openalex-snapshot
Cell Communications among Microorganisms, Plants, and Animals: Origin, Evolution, and Interplays
inferred← citeshttps://doi.org/10.3390/ijms24129872openalex-snapshot
Revealing the Roles of the JAZ Family in Defense Signaling and the Agarwood Formation Process in Aquilaria sinensis
inferred← citeshttps://doi.org/10.3390/molecules23092168openalex-snapshot
GC-MS Study of the Chemical Components of Different Aquilaria sinensis (Lour.) Gilgorgans and Agarwood from Different Asian Countries
inferred← citeshttps://doi.org/10.3390/molecules24071229openalex-snapshot
Smoke-Isolated Karrikins Stimulated Tanshinones Biosynthesis in Salvia miltiorrhiza through Endogenous Nitric Oxide and Jasmonic Acid
inferred← citeshttps://doi.org/10.3390/molecules29051075openalex-snapshot
Comparative Analysis of Metabolome and Transcriptome in Different Tissue Sites of Aquilaria sinensis (Lour.) Gilg
inferred← citeshttps://doi.org/10.3390/plants11182404openalex-snapshot
Single and Associated Effects of Drought and Heat Stresses on Physiological, Biochemical and Antioxidant Machinery of Four Eggplant Cultivars
inferred← citeshttps://doi.org/10.3390/plants12142631openalex-snapshot
Signal Mediators in the Implementation of Jasmonic Acid’s Protective Effect on Plants under Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/plants12244080openalex-snapshot
Jasmonate: A Hormone of Primary Importance for Temperature Stress Response in Plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.21228858openalex-snapshot
Additional file 1 of Comparative transcriptome analysis reveals different defence responses during the early stage of wounding stress in Chi-Nan germplasm and ordinary Aquilaria sinensis
inferred← citeshttps://doi.org/10.70675/02a20883zee26z4f1dz84fcz2fac436faa25openalex-snapshot
Étude de la biosynthèse des terpènes et de leur régulation chez Pelargonium x hybridum
inferred← citeshttps://doi.org/10.70675/cc1abb70zae93z4689za9c5z63ae281ef3afopenalex-snapshot
Les effets du changement climatique sur les émissions volatiles des grandes cultures et forêts du Sud de la France
inferred← citeshttps://doi.org/10.7287/peerj.11586v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11586v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11586v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.11586v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.11586v0.2/reviews/4openalex-snapshot
Peer Review #4 of "Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.11586v0.3/reviews/3openalex-snapshot
Peer Review #3 of "Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis (v0.3)"
inferred← citeshttps://doi.org/10.7287/peerj.11586v0.3/reviews/4openalex-snapshot
Peer Review #4 of "Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis (v0.3)"
inferred← citeshttps://doi.org/10.7287/peerj.15818v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15818v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15818v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15818v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.15818v0.3/reviews/1openalex-snapshot
Peer Review #1 of "Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis (v0.3)"
inferred← citeshttps://doi.org/10.7287/peerj.15818v0.3/reviews/3openalex-snapshot
Peer Review #3 of "Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis (v0.3)"
inferred← citeshttps://doi.org/10.7287/peerj.15818v0.4/reviews/1openalex-snapshot
Peer Review #1 of "Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis (v0.4)"
inferred← citeshttps://doi.org/10.7717/peerj.11586openalex-snapshot
Comparative anatomical and transcriptomic analyses of the color variation of leaves in Aquilaria sinensis
inferred← citeshttps://doi.org/10.7717/peerj.15818openalex-snapshot
Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis
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