| P50 | author | Jonathan Gershenzon | Q1506580 |
| | Annick Stintzi | Q58241512 |
| | Claus Wasternack | Q95951133 |
| | Louwrance P Wright | Q41810081 |
| | Andreas Schaller | Q42719616 |
| P2093 | author name string | Bettina Hause | |
| | Marko Bosch | |
| P2860 | cites work | Herbivory-induced volatiles function as defenses increasing fitness of the native plant Nicotiana attenuata in nature | Q21128798 |
| | Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves | Q24556763 |
| | Jasmonic acid levels are reduced in COMATOSE ATP-binding cassette transporter mutants. Implications for transport of jasmonate precursors into peroxisomes | Q46371050 |
| | Gibberellins, jasmonate and abscisic acid modulate the sucrose-induced expression of anthocyanin biosynthetic genes in Arabidopsis | Q46553004 |
| | Induction of the Arabidopsis PHO1;H10 gene by 12-oxo-phytodienoic acid but not jasmonic acid via a CORONATINE INSENSITIVE1-dependent pathway | Q46628436 |
| | Methyl jasmonate application induces increased densities of glandular trichomes on tomato, Lycopersicon esculentum | Q46678207 |
| | General detoxification and stress responses are mediated by oxidized lipids through TGA transcription factors in Arabidopsis | Q46707409 |
| | The role of JAR1 in Jasmonoyl-L: -isoleucine production during Arabidopsis wound response. | Q46774120 |
| | 12-oxo-phytodienoic acid triggers expression of a distinct set of genes and plays a role in wound-induced gene expression in Arabidopsis. | Q46781677 |
| | Identification of a peroxisomal acyl-activating enzyme involved in the biosynthesis of jasmonic acid in Arabidopsis | Q48084781 |
| | The rice hydroperoxide lyase OsHPL3 functions in defense responses by modulating the oxylipin pathway. | Q50498735 |
| | 12-oxo-phytodienoic acid accumulation during seed development represses seed germination in Arabidopsis. | Q51888292 |
| | Wound-Induced Proteinase Inhibitor in Plant Leaves: A Possible Defense Mechanism against Insects. | Q52683811 |
| | Systemic resistance induced by rhizosphere bacteria. | Q53901247 |
| | Jasmonate signaling mutants of Arabidopsis are susceptible to the soil fungus Pythium irregulare. | Q54117740 |
| | Reduced V-ATPase activity in the trans-Golgi network causes oxylipin-dependent hypocotyl growth Inhibition in Arabidopsis. | Q54535157 |
| | Jasmonic Acid Signaling Modulates Ozone-Induced Hypersensitive Cell Death | Q58055328 |
| | Ozone-Sensitive Arabidopsis rcd1 Mutant Reveals Opposite Roles for Ethylene and Jasmonate Signaling Pathways in Regulating Superoxide-Dependent Cell Death | Q58063708 |
| | JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling | Q58619723 |
| | Rapid effects of nitrogen form on leaf morphogenesis in tobacco | Q74155981 |
| | Quantitation of the octadecanoid 12-oxo-phytodienoic acid, a signalling compound in plant mechanotransduction | Q74168043 |
| | hpRNA-mediated targeting of the Arabidopsis FAD2 gene gives highly efficient and stable silencing | Q74607068 |
| | The Critical Requirement for Linolenic Acid Is Pollen Development, Not Photosynthesis, in an Arabidopsis Mutant | Q74806231 |
| | Differential induction of plant volatile biosynthesis in the lima bean by early and late intermediates of the octadecanoid-signaling pathway | Q78247078 |
| | A rapid method for isolating glandular trichomes | Q83272865 |
| | Distal transport of exogenously applied jasmonoyl-isoleucine with wounding stress | Q83296479 |
| | Transportation of de novo synthesized jasmonoyl isoleucine in tomato | Q84812058 |
| | Induction of wound response gene expression in tomato leaves by ionophores | Q43566635 |
| | Nuclear transport of plant potyviral proteins | Q43765680 |
| | Role of cis-12-oxo-phytodienoic acid in tomato embryo development | Q43782074 |
| | 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 | Q44052029 |
| | Jasmonate-dependent and COI1-independent defense responses against Sclerotinia sclerotiorum in Arabidopsis thaliana: auxin is part of COI1-independent defense signaling | Q44061566 |
| | Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors | Q44151621 |
| | Plant growth-promoting rhizobacteria systemically protect Arabidopsis thaliana against Cucumber mosaic virus by a salicylic acid and NPR1-independent and jasmonic acid-dependent signaling pathway | Q44362623 |
| | Reactive electrophile species activate defense gene expression in Arabidopsis | Q44402991 |
| | The role of octadecanoids and functional mimics in soybean defense responses. | Q44418087 |
| | Interspecific variation in terpenoid composition of defensive secretions of European Reticulitermes termites | Q44447781 |
| | The tomato suppressor of prosystemin-mediated responses2 gene encodes a fatty acid desaturase required for the biosynthesis of jasmonic acid and the production of a systemic wound signal for defense gene expression | Q44499538 |
| | The tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development | Q44701468 |
| | Peroxisomal Acyl-CoA synthetase activity is essential for seedling development in Arabidopsis thaliana | Q44741727 |
| | The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis | Q44982253 |
| | Jasmonic acid is a key regulator of spider mite-induced volatile terpenoid and methyl salicylate emission in tomato | Q45018140 |
| | Jasmonic acid control of GLABRA3 links inducible defense and trichome patterning in Arabidopsis | Q45350348 |
| | A rapid wound signal activates the systemic synthesis of bioactive jasmonates in Arabidopsis. | Q45994531 |
| | Jasmonate perception by inositol-phosphate-potentiated COI1-JAZ co-receptor | Q24569663 |
| | Crystal structure of 12-oxophytodienoate reductase 3 from tomato: self-inhibition by dimerization | Q24673341 |
| | Structural basis of substrate specificity of plant 12-oxophytodienoate reductases | Q27656910 |
| | Structural basis for prereceptor modulation of plant hormones by GH3 proteins | Q27679290 |
| | 12-Oxophytodienoate reductase 3 (OPR3) is the isoenzyme involved in jasmonate biosynthesis | Q28139398 |
| | The Arabidopsis male-sterile mutant, opr3, lacks the 12-oxophytodienoic acid reductase required for jasmonate synthesis | Q28145405 |
| | Characterization and cDNA-microarray expression analysis of 12-oxophytodienoate reductases reveals differential roles for octadecanoid biosynthesis in the local versus the systemic wound response | Q28215620 |
| | Insects betray themselves in nature to predators by rapid isomerization of green leaf volatiles | Q28291876 |
| | The DEFECTIVE IN ANTHER DEHISCIENCE gene encodes a novel phospholipase A1 catalyzing the initial step of jasmonic acid biosynthesis, which synchronizes pollen maturation, anther dehiscence, and flower opening in Arabidopsis | Q28361274 |
| | Plants attract parasitic wasps to defend themselves against insect pests by releasing hexenol | Q28469290 |
| | Distinct roles of jasmonates and aldehydes in plant-defense responses | Q28472455 |
| | Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany | Q30317845 |
| | An UPLC-MS/MS method for highly sensitive high-throughput analysis of phytohormones in plant tissues | Q30317951 |
| | Jasmonates: structural requirements for lipid-derived signals active in plant stress responses and development | Q30318828 |
| | Hydroxylated jasmonates are commonly occurring metabolites of jasmonic acid and contribute to a partial switch-off in jasmonate signaling. | Q30319727 |
| | Allene oxide cyclase dependence of the wound response and vascular bundle-specific generation of jasmonates in tomato - amplification in wound signalling. | Q30320705 |
| | Tissue-specific oxylipin signature of tomato flowers: allene oxide cyclase is highly expressed in distinct flower organs and vascular bundles | Q30321067 |
| | A special pair of phytohormones controls excitability, slow closure, and external stomach formation in the Venus flytrap | Q30504421 |
| | Jasmonate controls leaf growth by repressing cell proliferation and the onset of endoreduplication while maintaining a potential stand-by mode | Q33355374 |
| | Host recognition by the tobacco hornworm is mediated by a host plant compound. | Q33946271 |
| | Plant defense in the absence of jasmonic acid: the role of cyclopentenones. | Q33948155 |
| | Distinct roles for jasmonate synthesis and action in the systemic wound response of tomato | Q34029515 |
| | (+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate | Q34606303 |
| | 12-hydroxyjasmonic acid glucoside is a COI1-JAZ-independent activator of leaf-closing movement in Samanea saman | Q34626273 |
| | The JAZ family of repressors is the missing link in jasmonate signalling. | Q34652938 |
| | Tomato, pests, parasitoids, and predators: tritrophic interactions involving the genus Lycopersicon | Q34795883 |
| | Changing green leaf volatile biosynthesis in plants: an approach for improving plant resistance against both herbivores and pathogens. | Q35130656 |
| | Cytochromes P450 CYP94C1 and CYP94B3 catalyze two successive oxidation steps of plant hormone Jasmonoyl-isoleucine for catabolic turnover | Q35839023 |
| | Catabolism and deactivation of the lipid-derived hormone jasmonoyl-isoleucine | Q35970237 |
| | Airborne signals prime plants against insect herbivore attack | Q36162493 |
| | Green leaf volatiles: hydroperoxide lyase pathway of oxylipin metabolism | Q36440682 |
| | Improved herbivore resistance in cultivated tomato with the sesquiterpene biosynthetic pathway from a wild relative | Q36471313 |
| | Hydroperoxide lyase depletion in transgenic potato plants leads to an increase in aphid performance | Q36542596 |
| | Intrinsic acyl-CoA thioesterase activity of a peroxisomal ATP binding cassette transporter is required for transport and metabolism of fatty acids | Q36567914 |
| | Feeding-induced rearrangement of green leaf volatiles reduces moth oviposition | Q36845366 |
| | Cyclophilin 20-3 relays a 12-oxo-phytodienoic acid signal during stress responsive regulation of cellular redox homeostasis. | Q36915510 |
| | Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant | Q37123878 |
| | Jasmonate passes muster: a receptor and targets for the defense hormone | Q37331758 |
| | Oxylipins: structurally diverse metabolites from fatty acid oxidation. | Q37376645 |
| | The wound hormone jasmonate | Q37442532 |
| | Enzymes in jasmonate biosynthesis - structure, function, regulation. | Q37585789 |
| | The JAZ proteins: a crucial interface in the jasmonate signaling cascade | Q37941330 |
| | JAZ repressors and the orchestration of phytohormone crosstalk | Q37960211 |
| | Transcriptional machineries in jasmonate-elicited plant secondary metabolism. | Q37998268 |
| | ROS-mediated lipid peroxidation and RES-activated signaling | Q38085650 |
| | Plants on early alert: glandular trichomes as sensors for insect herbivores | Q38434328 |
| | Co(i)-ordinating defenses: NaCOI1 mediates herbivore- induced resistance in Nicotiana attenuata and reveals the role of herbivore movement in avoiding defenses | Q39340915 |
| | Systemin--a polypeptide defense signal in plants | Q40964855 |
| | The arabidopsis DELAYED DEHISCENCE1 gene encodes an enzyme in the jasmonic acid synthesis pathway | Q41748309 |
| | Tomato linalool synthase is induced in trichomes by jasmonic acid | Q41833820 |
| | Wound-induced endogenous jasmonates stunt plant growth by inhibiting mitosis | Q41847634 |
| | TGA transcription factors and jasmonate-independent COI1 signalling regulate specific plant responses to reactive oxylipins | Q41874350 |
| | Oxylipin Signaling: A Distinct Role for the Jasmonic Acid Precursor cis-(+)-12-Oxo-Phytodienoic Acid (cis-OPDA). | Q41955692 |
| | Role of trichomes in defense against herbivores: comparison of herbivore response to woolly and hairless trichome mutants in tomato (Solanum lycopersicum). | Q42013286 |
| | JA-Ile signalling in Solanum nigrum is not required for defence responses in nature | Q42016040 |
| | Intronic T-DNA insertion renders Arabidopsis opr3 a conditional jasmonic acid-producing mutant. | Q42017630 |
| | Systemin and jasmonic acid regulate constitutive and herbivore-induced systemic volatile emissions in tomato, Solanum lycopersicum | Q42019275 |
| | The tomato odorless-2 mutant is defective in trichome-based production of diverse specialized metabolites and broad-spectrum resistance to insect herbivores. | Q42020276 |
| | Jasmonate and ppHsystemin regulate key Malonylation steps in the biosynthesis of 17-Hydroxygeranyllinalool Diterpene Glycosides, an abundant and effective direct defense against herbivores in Nicotiana attenuata | Q42022299 |
| | Priming defense genes and metabolites in hybrid poplar by the green leaf volatile cis-3-hexenyl acetate. | Q42028191 |
| | Comparisons of LIPOXYGENASE3- and JASMONATE-RESISTANT4/6-silenced plants reveal that jasmonic acid and jasmonic acid-amino acid conjugates play different roles in herbivore resistance of Nicotiana attenuata | Q42031148 |
| | Silencing threonine deaminase and JAR4 in Nicotiana attenuata impairs jasmonic acid-isoleucine-mediated defenses against Manduca sexta | Q42035573 |
| | Reduced levels of volatile emissions in jasmonate-deficient spr2 tomato mutants favour oviposition by insect herbivores. | Q42035597 |
| | A feeding stimulant for Manduca sexta from Solanum surattenses | Q42035606 |
| | Role of beta-oxidation in jasmonate biosynthesis and systemic wound signaling in tomato | Q42042053 |
| | Silencing of hydroperoxide lyase and allene oxide synthase reveals substrate and defense signaling crosstalk in Nicotiana attenuata | Q42043729 |
| | Silencing the jasmonate cascade: induced plant defenses and insect populations | Q42044346 |
| | Defensive function of herbivore-induced plant volatile emissions in nature. | Q42054565 |
| | An octadecanoid pathway mutant (JL5) of tomato is compromised in signaling for defense against insect attack | Q42063416 |
| | The transcriptome of cis-jasmone-induced resistance in Arabidopsis thaliana and its role in indirect defence | Q42936811 |
| | The moss Physcomitrella patens contains cyclopentenones but no jasmonates: mutations in allene oxide cyclase lead to reduced fertility and altered sporophyte morphology. | Q42939544 |
| | The Arabidopsis CORONATINE INSENSITIVE1 protein is a jasmonate receptor. | Q43283579 |
| | Antagonism between herbivore-induced plant volatiles and trichomes affects tritrophic interactions | Q43438525 |
| | GLUTAMATE RECEPTOR-LIKE genes mediate leaf-to-leaf wound signalling | Q43491131 |
| | 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 | Q43564424 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | herbivore | Q59099 |
| | herbivory | Q45874067 |
| P1104 | number of pages | 15 | |
| P304 | page(s) | 396-410 | |
| P577 | publication date | 2014-07-29 | |
| P1433 | published in | Plant Physiology | Q3906288 |
| P1476 | title | Jasmonic acid and its precursor 12-oxophytodienoic acid control different aspects of constitutive and induced herbivore defenses in tomato | |
| P478 | volume | 166 | |