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Dynamics and origin of cytokinins involved in plant manipulation by a leaf‐mining insect
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118867716.ch7openalex-snapshot
Regulation of Abiotic and Biotic Stress Responses by Plant Hormones
inferredcites →https://doi.org/10.1002/ece3.1580openalex-snapshot
Correlation between the green‐island phenotype and Wolbachia infections during the evolutionary diversification of Gracillariidae leaf‐mining moths
inferredcites →https://doi.org/10.1007/bf02860866openalex-snapshot
Cytokinin production by microorganisms
inferredcites →https://doi.org/10.1007/s00344-010-9177-5openalex-snapshot
Feeding by Hessian Fly (Mayetiola destructor [Say]) Larvae on Wheat Increases Levels of Fatty Acids and Indole-3-Acetic Acid but not Hormones Involved in Plant-Defense Signaling
inferredcites →https://doi.org/10.1007/s10886-013-0307-yopenalex-snapshot
Leaf-Miners Co-opt Microorganisms to Enhance their Nutritional Environment
inferredcites →https://doi.org/10.1007/s10886-014-0457-6openalex-snapshot
Phytohormone Dynamics Associated with Gall Insects, and their Potential Role in the Evolution of the Gall-Inducing Habit
inferredcites →https://doi.org/10.1007/s10886-014-0466-5openalex-snapshot
Cytokinin-Induced Phenotypes in Plant-Insect Interactions: Learning from the Bacterial World
inferredcites →https://doi.org/10.1007/s11103-008-9435-0openalex-snapshot
Role of plant hormones in plant defence responses
inferredcites →https://doi.org/10.1007/s11627-000-0021-7openalex-snapshot
Cytokinins: Biosynthesis metabolism and perception
inferredcites →https://doi.org/10.1007/s11829-010-9120-5openalex-snapshot
Feeding by a gall-inducing caterpillar species alters levels of indole-3-acetic and abscisic acid in Solidago altissima (Asteraceae) stems
inferredcites →https://doi.org/10.1007/s11829-014-9309-0openalex-snapshot
Exogenous phytohormones and the induction of plant galls by insects
inferredcites →https://doi.org/10.1007/s11829-014-9349-5openalex-snapshot
Hypermetamorphosis in a leaf-miner allows insects to cope with a confined nutritional space
inferredcites →https://doi.org/10.1016/0006-291x(74)90292-7openalex-snapshot
Unique presence of 2-methylthio-ribosylzeatin in the transfer ribonucleic acid of the bacterium Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1016/bs.abr.2016.09.007openalex-snapshot
Influence of Microbial Symbionts on Plant–Insect Interactions
inferredcites →https://doi.org/10.1016/j.aca.2010.09.020openalex-snapshot
Analysis of 2-methylthio-derivatives of isoprenoid cytokinins by liquid chromatography–tandem mass spectrometry
inferredcites →https://doi.org/10.1016/j.jinsphys.2015.06.003openalex-snapshot
Leaf-mining by Phyllonorycter blancardella reprograms the host-leaf transcriptome to modulate phytohormones associated with nutrient mobilization and plant defense
inferredcites →https://doi.org/10.1016/j.jinsphys.2015.12.009openalex-snapshot
Insect-induced effects on plants and possible effectors used by galling and leaf-mining insects to manipulate their host-plant
inferredcites →https://doi.org/10.1016/j.tplants.2008.01.003openalex-snapshot
Cytokinin: secret agent of symbiosis
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.003openalex-snapshot
Cytokinins and plant immunity: old foes or new friends?
inferredcites →https://doi.org/10.1016/j.tplants.2012.01.003openalex-snapshot
Role of phytohormones in insect-specific plant reactions
inferredcites →https://doi.org/10.1016/j.tree.2012.08.013openalex-snapshot
Insect symbionts as hidden players in insect–plant interactions
inferredcites →https://doi.org/10.1016/j.virol.2010.03.023openalex-snapshot
The Interaction between geminivirus pathogenicity proteins and adenosine kinase leads to increased expression of primary cytokinin-responsive genes
inferredcites →https://doi.org/10.1016/s0015-3796(17)31102-2openalex-snapshot
Cytokinin Activity in Larval Infected Leaves
inferredcites →https://doi.org/10.1016/s0031-9422(00)91263-9openalex-snapshot
Synthesis of 2-methylthio-cis- and trans-ribosylzeatin and their isolation from Pisum tRNA
inferredcites →https://doi.org/10.1016/s0166-2481(08)70217-4openalex-snapshot
Production of Plant Growth Regulators by Non-Mycorrhizal Fungi Associated With The Roots of Forest Trees
inferredcites →https://doi.org/10.1023/a:1010733617543openalex-snapshot
Cytokinins and auxins in plant-pathogen interactions – An overview
inferredcites →https://doi.org/10.1038/223319a0openalex-snapshot
Leaf-miner Caterpillars and Cytokinins in the “Green Islands” of Autumn Leaves
inferredcites →https://doi.org/10.1038/nchembio.165openalex-snapshot
Plant hormones are versatile chemical regulators of plant growth
inferredcites →https://doi.org/10.1046/j.1469-8137.2001.00158.xopenalex-snapshot
Cytokinins in the ball gall ofSolidago altissimaand in the gall forming larvae ofEurosta solidaginis
inferredcites →https://doi.org/10.1046/j.1469-8137.2001.00161.xopenalex-snapshot
Indole‐3‐acetic acid and ball gall development on Solidago altissima
inferredcites →https://doi.org/10.1071/fp11276openalex-snapshot
Cytokinins – recent news and views of evolutionally old molecules
inferredcites →https://doi.org/10.1073/pnas.0500793102openalex-snapshot
Agrobacterium tumefaciens increases cytokinin production in plastids by modifying the biosynthetic pathway in the host plant
inferredcites →https://doi.org/10.1073/pnas.0811683106openalex-snapshot
Identification of Rhodococcus fascians cytokinins and their modus operandi to reshape the plant
inferredcites →https://doi.org/10.1073/pnas.70.12.3825openalex-snapshot
Isolation of cis -Zeatin from Corynebacterium fascians Cultures
inferredcites →https://doi.org/10.1080/17429145.2010.484552openalex-snapshot
Gall-inducingPachypsylla celtidis(Psyllidae) infiltrate hackberry trees with high concentrations of phytohormones
inferredcites →https://doi.org/10.1086/303388openalex-snapshot
Geometrical Games between a Host and a Parasitoid
inferredcites →https://doi.org/10.1086/417659openalex-snapshot
The Dilemma of Plants: To Grow or Defend
inferredcites →https://doi.org/10.1093/jxb/erq457openalex-snapshot
Distribution, biological activities, metabolism, and the conceivable function of cis-zeatin-type cytokinins in plants
inferredcites →https://doi.org/10.1093/jxb/eru435openalex-snapshot
Plant-insect interactions under bacterial influence: ecological implications and underlying mechanisms
inferredcites →https://doi.org/10.1093/jxb/erv214openalex-snapshot
The role of cis -zeatin-type cytokinins in plant growth regulation and mediating responses to environmental interactions
inferredcites →https://doi.org/10.1094/mpmi-02-13-0054-ropenalex-snapshot
Bioactive Cytokinins Are Selectively Secreted by Sinorhizobium meliloti Nodulating and Nonnodulating Strains
inferredcites →https://doi.org/10.1094/mpmi-03-13-0076-ropenalex-snapshot
Rhizobial Synthesized Cytokinins Contribute to But Are Not Essential for the Symbiotic Interaction Between Photosynthetic Bradyrhizobia and Aeschynomene Legumes
inferredcites →https://doi.org/10.1098/rsbl.2007.0051openalex-snapshot
Cytokinin-mediated leaf manipulation by a leafminer caterpillar
inferredcites →https://doi.org/10.1098/rspb.2010.0214openalex-snapshot
Plant green-island phenotype induced by leaf-miners is mediated by bacterial symbionts
inferredcites →https://doi.org/10.1104/pp.102.3.867openalex-snapshot
Partial Purification of a cis-trans-Isomerase of Zeatin from Immature Seed of Phaseolus vulgaris L
inferredcites →https://doi.org/10.1104/pp.103.037176openalex-snapshot
Molecular Characterization of Cytokinin-Responsive Histidine Kinases in Maize. Differential Ligand Preferences and Response to cis-Zeatin
inferredcites →https://doi.org/10.1104/pp.107.095596openalex-snapshot
Resistance to Botrytis cinerea Induced in Arabidopsis by Elicitors Is Independent of Salicylic Acid, Ethylene, or Jasmonate Signaling But Requires PHYTOALEXIN DEFICIENT3
inferredcites →https://doi.org/10.1104/pp.123.4.1593openalex-snapshot
The Forms and Sources of Cytokinins in Developing White Lupine Seeds and Fruits
inferredcites →https://doi.org/10.1104/pp.58.6.749openalex-snapshot
Cytokinins in Corynebacterium fascians Cultures
inferredcites →https://doi.org/10.1104/pp.92.3.565openalex-snapshot
Cytokinins and Flower Bud Formation in Vitro in Tobacco
inferredcites →https://doi.org/10.1105/tpc.114.133595openalex-snapshot
The Yin-Yang of Hormones: Cytokinin and Auxin Interactions in Plant Development
inferredcites →https://doi.org/10.1105/tpc.12.11.2175openalex-snapshot
Roles of Salicylic Acid, Jasmonic Acid, and Ethylene in cpr-Induced Resistance in Arabidopsis
inferredcites →https://doi.org/10.1111/1365-2435.12042openalex-snapshot
Cytokinins as key regulators in plant–microbe–insect interactions: connecting plant growth and defence
inferredcites →https://doi.org/10.1111/1365-2435.12100openalex-snapshot
Three‐way interactions between plants, microbes and insects
inferredcites →https://doi.org/10.1111/1574-6968.12119openalex-snapshot
The leafy gall syndrome induced byRhodococcus fascians
inferredcites →https://doi.org/10.1111/j.1365-3032.2009.00702.xopenalex-snapshot
Sexually dimorphic gall structures correspond to differential phytohormone contents in male and female wasp larvae
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04482.xopenalex-snapshot
Cytokinin promotes flowering of Arabidopsis via transcriptional activation of the FT paralogue TSF
inferredcites →https://doi.org/10.1111/j.1469-185x.2007.00033.xopenalex-snapshot
Are green islands red herrings? Significance of green islands in plant interactions with pathogens and pests
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04264.xopenalex-snapshot
Phytohormones and willow gall induction by a gall‐inducing sawfly
inferredcites →https://doi.org/10.1111/ppa.12629openalex-snapshot
Fungal derived cytokinins are necessary for normal Ustilago maydis infection of maize
inferredcites →https://doi.org/10.1111/tpj.13167openalex-snapshot
Transcriptome dynamics of Arabidopsis during sequential biotic and abiotic stresses
inferredcites →https://doi.org/10.1128/mmbr.52.1.103-113.1988openalex-snapshot
Thionucleosides in transfer ribonucleic acid: diversity, structure, biosynthesis, and function
inferredcites →https://doi.org/10.1139/b06-149openalex-snapshot
cis-Cytokinins that predominate inPisum sativumduring early embryogenesis will accelerate embryo growth in vitro
inferredcites →https://doi.org/10.1146/annurev-phyto-072910-095217openalex-snapshot
A Successful Bacterial Coup d'État: How Rhodococcus fascians Redirects Plant Development
inferredcites →https://doi.org/10.1146/annurev.arplant.52.1.89openalex-snapshot
C YTOKININ M ETABOLISM AND A CTION
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105231openalex-snapshot
CYTOKININS: Activity, Biosynthesis, and Translocation
inferredcites →https://doi.org/10.1186/1746-4811-8-1openalex-snapshot
Precursor uptake assays and metabolic analyses in isolated tomato fruit chromoplasts
inferredcites →https://doi.org/10.1186/1746-4811-8-42openalex-snapshot
Concurrent profiling of indole-3-acetic acid, abscisic acid, and cytokinins and structurally related purines by high-performance-liquid-chromatography tandem electrospray mass spectrometry
inferredcites →https://doi.org/10.1271/bbb.130406openalex-snapshot
Phytohormones in Japanese Mugwort Gall Induction by a Gall-Inducing Gall Midge
inferredcites →https://doi.org/10.1371/journal.pone.0062350openalex-snapshot
Phytohormones Related to Host Plant Manipulation by a Gall-Inducing Leafhopper
inferredcites →https://doi.org/10.21273/hortsci.9.5.458openalex-snapshot
Isolation of Zeatin from Larvae of Dryocosmus kuriphilus Yasumatsu1
inferredcites →https://doi.org/10.2307/3079148openalex-snapshot
Geometrical Games between a Host and a Parasitoid
inferredcites →https://doi.org/10.4039/entm10377fvopenalex-snapshot
THE BIOLOGY AND DYNAMICS OFLITHOCOLLETIS BLANCARDELLA(LEPIDOPTERA: GRACILLARIIDAE) ON APPLE IN QUEBEC
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.4760197openalex-extracted
Combination of Functional Plants Conserves Predators, Repels Pests, and Enhances Biological Control of Aphis Spiraecola In Apple Orchards
inferred← citeshttps://doi.org/10.1007/s00239-021-10035-zopenalex-snapshot
Evolution of the Cytokinin Dehydrogenase (CKX) Domain
inferred← citeshttps://doi.org/10.1007/s00344-026-12263-3openalex-snapshot
Targeted Profiling of Signaling Molecules in Papaver rhoeas L. Reveals that Onset and Control of Benzylisoquinoline Alkaloid Biosynthesis Corresponds with Cytokinins, Independent of Light
inferred← citeshttps://doi.org/10.1007/s00709-018-01339-xopenalex-snapshot
Correction to: How the activity of natural enemies changes the structure and metabolism of the nutritive tissue in galls? Evidence from the Palaeomystella oligophaga (Lepidoptera) -Macairea radula (Metastomataceae) system
inferred← citeshttps://doi.org/10.1007/s00709-018-1321-2openalex-snapshot
How the activity of natural enemies changes the structure and metabolism of the nutritive tissue in galls? Evidence from the Palaeomystella oligophaga (Lepidoptera) -Macairea radula (Metastomataceae) system
inferred← citeshttps://doi.org/10.1007/s10811-023-03068-yopenalex-snapshot
Phytohormonal impacts on fatty acid profiles in Chlorella vulgaris Beijerinck: endogenous identification and exogenous application of cytokinins and abscisic acid
inferred← citeshttps://doi.org/10.1007/s11829-021-09817-5openalex-snapshot
The localization of phytohormones within the gall-inducing insect Eurosta solidaginis (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1007/s11829-021-09858-wopenalex-snapshot
Effects of a saponin-based insect resistance and a systemic pathogen resistance on field performance of the wild crucifer Barbarea vulgaris
inferred← citeshttps://doi.org/10.1016/b978-0-323-91886-2.00003-3openalex-snapshot
Regulatory role of phytohormones in the interaction of plants with insect herbivores
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2024.105512openalex-snapshot
Combination of functional plants conserves predators, repels pests, and enhances biological control of Aphis spiraecola in apple orchards
inferred← citeshttps://doi.org/10.1016/j.cbd.2021.100867openalex-snapshot
Detoxification gene families in Phylloxera: Endogenous functions and roles in response to the environment
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111188openalex-snapshot
Review: Trait plasticity during plant-insect interactions: From molecular mechanisms to impact on community dynamics
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.166139openalex-snapshot
Floral resources and ground covers promote natural enemies but not pest insects in apple orchards: A global meta-analysis
inferred← citeshttps://doi.org/10.1038/s41598-022-07535-3openalex-snapshot
Symbiotic bacteria of the gall-inducing mite Fragariocoptes setiger (Eriophyoidea) and phylogenomic resolution of the eriophyoid position among Acari
inferred← citeshttps://doi.org/10.1094/mpmi-11-18-0301-ropenalex-snapshot
Heritable Phytohormone Profiles of Poplar Genotypes Vary in Resistance to a Galling Aphid
inferred← citeshttps://doi.org/10.1101/777334openalex-snapshot
Manipulation of plant primary metabolism by leaf-mining larvae in the race against leaf senescence
inferred← citeshttps://doi.org/10.1101/777367openalex-snapshot
Field application of the geometric framework reveals a multistep strategy of nutrient regulation in a leaf-miner
inferred← citeshttps://doi.org/10.1111/1744-7917.12536openalex-snapshot
The promises and challenges of research on plant–insect–microbe interactions
inferred← citeshttps://doi.org/10.1111/eea.12681openalex-snapshot
Modulation of plant cytokinin levels in the W olbachia‐free leaf‐mining species P hyllonorycter mespilella
inferred← citeshttps://doi.org/10.1111/mec.15745openalex-snapshot
Host plant diet affects growth and induces altered gene expression and microbiome composition in the wood white (Leptidea sinapis) butterfly
inferred← citeshttps://doi.org/10.1111/nph.20154openalex-snapshot
Leaf mining induced chemical defense of a Late Triassic ginkgophyte plant
inferred← citeshttps://doi.org/10.1139/cjb-2017-0178openalex-snapshot
Phytohormone profiling reveals fungal signatures and strong manipulation of infection cycle in the Gymnosporangium juniper-virginianae dual-host plant system
inferred← citeshttps://doi.org/10.1146/annurev-ento-020425-073850openalex-snapshot
Insect Production and Secretion of Phytohormones and Impacts on Host Plants
inferred← citeshttps://doi.org/10.1146/annurev-phyto-010820-012722openalex-snapshot
Gall-Inducing Parasites: Convergent and Conserved Strategies of Plant Manipulation by Insects and Nematodes
inferred← citeshttps://doi.org/10.20546/ijcmas.2019.808.321openalex-snapshot
Cytokinin Induction in Response to Tomato Pinworm, Tuta absoluta Meyrick (Gelechiidae: Lepidoptera) Damage on Tomato Leaves
inferred← citeshttps://doi.org/10.21203/rs.3.rs-821190/v1openalex-snapshot
Genome and Metagenome of The Phytophagous Gall-Inducing Mite Fragariocoptes Setiger (Eriophyoidea): Are Symbiotic Bacteria Responsible For Gall-Formation?
inferred← citeshttps://doi.org/10.21684/0132-8077-2024-32-1-43-57openalex-snapshot
ADVANCES IN THE STUDY OF MITE GALLOGENESIS AND ITS COMPARISON WITH THE DEVELOPMENT OF INSECT-INDUCED GALLS
inferred← citeshttps://doi.org/10.3389/fpls.2019.01777openalex-snapshot
Role of Cytokinins for Interactions of Plants With Microbial Pathogens and Pest Insects
inferred← citeshttps://doi.org/10.3390/ijms24119613openalex-snapshot
Genomic Assessment of the Contribution of the Wolbachia Endosymbiont of Eurosta solidaginis to Gall Induction
inferred← citeshttps://doi.org/10.3390/insects14060489openalex-snapshot
Abscisic Acid: A Potential Secreted Effector Synthesized by Phytophagous Insects for Host-Plant Manipulation
inferred← citeshttps://doi.org/10.3390/plants9020208openalex-snapshot
Cytokinins Are Abundant and Widespread among Insect Species
inferred← citeshttps://doi.org/10.70675/ba328d98z1a25z44d8z9c3ez6ac7e9eb6573openalex-snapshot
Evolutionary origin and molecular bases of the gall-inducing life-style in the Gracillariidae
inferred← citeshttps://doi.org/10.7554/elife.36268openalex-snapshot
Cytokinin transfer by a free-living mirid to Nicotiana attenuata recapitulates a strategy of endophytic insects
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