review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Gregg A Howe | Q88040843 |
P2093 | author name string | John Browse | |
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Mechanism of auxin perception by the TIR1 ubiquitin ligase | Q27644361 | ||
The systemin signaling pathway: differential activation of plant defensive genes | Q28138073 | ||
Systemic wound signaling in tomato leaves is cooperatively regulated by systemin and hydroxyproline-rich glycopeptide signals | Q28250927 | ||
The F-box protein TIR1 is an auxin receptor | Q28253006 | ||
Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens | Q29616814 | ||
Hydroxylated jasmonates are commonly occurring metabolites of jasmonic acid and contribute to a partial switch-off in jasmonate signaling. | Q30319727 | ||
Jasmonates: an update on biosynthesis, signal transduction and action in plant stress response, growth and development | Q30319824 | ||
The wound response in tomato--role of jasmonic acid | Q30320111 | ||
Different transcript patterns in response to specialist and generalist herbivores in the wild Arabidopsis relative Boechera divaricarpa | Q33303687 | ||
The tify family previously known as ZIM. | Q33344031 | ||
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 | ||
The Arabidopsis F-box protein TIR1 is an auxin receptor | Q34557948 | ||
Plant immunity to insect herbivores | Q34585236 | ||
Cross talk in defense signaling. | Q34589015 | ||
The JAZ family of repressors is the missing link in jasmonate signalling. | Q34652938 | ||
Plant responses to insect herbivory: the emerging molecular analysis. | Q34833724 | ||
Coordinated plant defense responses in Arabidopsis revealed by microarray analysis. | Q35336355 | ||
Systemic signaling in the wound response | Q36154065 | ||
Jasmonate-induced responses are costly but benefit plants under attack in native populations | Q36167823 | ||
Jasmonate: an oxylipin signal with many roles in plants | Q36402800 | ||
A role for jasmonate in pathogen defense of Arabidopsis. | Q36516374 | ||
Jasmonate is essential for insect defense in Arabidopsis | Q36773611 | ||
Jasmonate signalling network in Arabidopsis thaliana: crucial regulatory nodes and new physiological scenarios | Q37016296 | ||
Plant defense priming against herbivores: getting ready for a different battle | Q37100624 | ||
Recognition of herbivory-associated molecular patterns | Q37100629 | ||
Avoiding effective defenses: strategies employed by phloem-feeding insects | Q37100646 | ||
Interactions between arthropod-induced aboveground and belowground defenses in plants | Q37100650 | ||
Co(i)-ordinating defenses: NaCOI1 mediates herbivore- induced resistance in Nicotiana attenuata and reveals the role of herbivore movement in avoiding defenses | Q39340915 | ||
Facing the future of plant-insect interaction research: le retour à la "raison d'être". | Q40117368 | ||
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 | ||
Signaling pathways controlling induced resistance to insect herbivores in Arabidopsis. | Q42031455 | ||
Resistance management in a native plant: nicotine prevents herbivores from compensating for plant protease inhibitors | Q42033363 | ||
Stability of plant defense proteins in the gut of insect herbivores. | Q42033823 | ||
Herbivory rapidly activates MAPK signaling in attacked and unattacked leaf regions but not between leaves of Nicotiana attenuata | Q42033897 | ||
Functional diversification of acyl-coenzyme A oxidases in jasmonic acid biosynthesis and action. | Q42035120 | ||
Silencing threonine deaminase and JAR4 in Nicotiana attenuata impairs jasmonic acid-isoleucine-mediated defenses against Manduca sexta | Q42035573 | ||
Role of beta-oxidation in jasmonate biosynthesis and systemic wound signaling in tomato | Q42042053 | ||
A conserved transcript pattern in response to a specialist and a generalist herbivore | Q42043395 | ||
Polyphenol oxidase overexpression in transgenic Populus enhances resistance to herbivory by forest tent caterpillar (Malacosoma disstria). | Q42043911 | ||
Silencing the jasmonate cascade: induced plant defenses and insect populations | Q42044346 | ||
An octadecanoid pathway mutant (JL5) of tomato is compromised in signaling for defense against insect attack | Q42063416 | ||
Silverleaf whitefly induces salicylic acid defenses and suppresses effectual jasmonic acid defenses | Q42506071 | ||
COI1: an Arabidopsis gene required for jasmonate-regulated defense and fertility | Q42677452 | ||
Resistance of cultivated tomato to cell content-feeding herbivores is regulated by the octadecanoid-signaling pathway | Q44134005 | ||
Constitutive activation of jasmonate signaling in an Arabidopsis mutant correlates with enhanced resistance to Erysiphe cichoracearum, Pseudomonas syringae, and Myzus persicae | Q44220055 | ||
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 | ||
Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth-related transcriptional reorganization in Nicotiana attenuata | Q44693284 | ||
The tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development | Q44701468 | ||
JASMONATE-INSENSITIVE1 encodes a MYC transcription factor essential to discriminate between different jasmonate-regulated defense responses in Arabidopsis. | Q44945509 | ||
The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis | Q44982253 | ||
Major signaling pathways modulate Arabidopsis glucosinolate accumulation and response to both phloem-feeding and chewing insects | Q46516505 | ||
Expression profiling reveals COI1 to be a key regulator of genes involved in wound- and methyl jasmonate-induced secondary metabolism, defence, and hormone interactions | Q46602131 | ||
Signal signature and transcriptome changes of Arabidopsis during pathogen and insect attack. | Q46707236 | ||
Transcriptional regulators of stamen development in Arabidopsis identified by transcriptional profiling. | Q52013827 | ||
Differential gene expression in response to mechanical wounding and insect feeding in Arabidopsis. | Q52579034 | ||
Wound-Induced Proteinase Inhibitor in Plant Leaves: A Possible Defense Mechanism against Insects. | Q52683811 | ||
Jasmonate signaling mutants of Arabidopsis are susceptible to the soil fungus Pythium irregulare. | Q54117740 | ||
Arabidopsis Mutants Selected for Resistance to the Phytotoxin Coronatine Are Male Sterile, Insensitive to Methyl Jasmonate, and Resistant to a Bacterial Pathogen. | Q54205776 | ||
A downstream mediator in the growth repression limb of the jasmonate pathway | Q57232384 | ||
JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling | Q58619723 | ||
The Critical Requirement for Linolenic Acid Is Pollen Development, Not Photosynthesis, in an Arabidopsis Mutant | Q74806231 | ||
Arabidopsis ZIM, a plant-specific GATA factor, can function as a transcriptional activator | Q79331869 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | insect | Q1390 |
P1104 | number of pages | 7 | |
P304 | page(s) | 832-838 | |
P577 | publication date | 2008-03-01 | |
P1433 | published in | Plant Physiology | Q3906288 |
P1476 | title | New weapons and a rapid response against insect attack | |
P478 | volume | 146 |