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Myzus persicae resistance to neonicotinoids—unravelling the contribution of different mechanisms to phenotype
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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/ps.1409openalex-snapshot
Insecticide resistance status of Myzus persicae (Hemiptera: Aphididae) populations from peach and tobacco in mainland Greece
inferredcites →https://doi.org/10.1002/ps.1888openalex-snapshot
Metabolic enzyme(s) confer imidacloprid resistance in a clone of Myzus persicae (Sulzer) (Hemiptera: Aphididae) from Greece
inferredcites →https://doi.org/10.1002/ps.1929openalex-snapshot
Monitoring for imidacloprid resistance in the tobacco‐adapted form of the green peach aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae), in the eastern United States
inferredcites →https://doi.org/10.1002/ps.2224openalex-snapshot
Uncommon associations in target resistance among French populations of Myzus persicae from oilseed rape crops
inferredcites →https://doi.org/10.1002/ps.2307openalex-snapshot
Identifying the presence of neonicotinoidresistant peach‐potato aphid ( Myzus persicae ) in the peach‐growing regions of southern France and northern Spain
inferredcites →https://doi.org/10.1002/ps.3630openalex-snapshot
Detecting the presence of target‐site resistance to neonicotinoids and pyrethroids in Italian populations of Myzus persicae
inferredcites →https://doi.org/10.1002/ps.3895openalex-snapshot
Insect P450 inhibitors and insecticides: challenges and opportunities
inferredcites →https://doi.org/10.1002/ps.4495openalex-snapshot
Discovery of metabolic resistance to neonicotinoids in green peach aphids (Myzus persicae) in Australia
inferredcites →https://doi.org/10.1002/ps.4833openalex-snapshot
Occurrence of target‐site resistance to neonicotinoids in the aphid Myzus persicae in Tunisia, and its status on different host plants
inferredcites →https://doi.org/10.1002/ps.570openalex-snapshot
Variation in response to neonicotinoid insecticides in peach‐potato aphids, Myzus persicae (Hemiptera: Aphididae)
inferredcites →https://doi.org/10.1002/ps.6558openalex-snapshot
Molecular innovations underlying resistance to nicotine and neonicotinoids in the aphid Myzus persicae
inferredcites →https://doi.org/10.1002/ps.6768openalex-snapshot
V101I and R81T mutations in the nicotinic acetylcholine receptor β1 subunit are associated with neonicotinoid resistance in Myzus persicae
inferredcites →https://doi.org/10.1002/ps.6778openalex-snapshot
Target site mutations underlying insecticide resistance in Tunisian populations of Myzus persicae (Sulzer) on peach orchards and potato crops
inferredcites →https://doi.org/10.1002/ps.7362openalex-snapshot
P450 ‐mediated resistance in Myzus persicae (Sulzer) (Hemiptera: Aphididae) reduces the efficacy of neonicotinoid seed treatments in Brassica napus
inferredcites →https://doi.org/10.1006/pest.1998.2373openalex-snapshot
Association between Biochemical Markers and Insecticide Resistance in the Cotton Aphid,Aphis gossypiiGlover
inferredcites →https://doi.org/10.1007/s10340-020-01210-0openalex-snapshot
Insecticide resistance and its management in Bemisia tabaci species
inferredcites →https://doi.org/10.1016/0048-3575(82)90110-9openalex-snapshot
A carboxylesterase with broad substrate specificity causes organophosphorus, carbamate and pyrethroid resistance in peach-potato aphids (Myzus persicae)
inferredcites →https://doi.org/10.1016/0742-8413(91)90003-copenalex-snapshot
Insect resistance to insecticides: Mechanisms and diagnosis
inferredcites →https://doi.org/10.1016/j.aspen.2015.01.010openalex-snapshot
Two mutations in nAChR beta subunit is associated with imidacloprid resistance in the Aphis gossypii
inferredcites →https://doi.org/10.1016/j.ibmb.2008.07.007openalex-snapshot
Organophosphates' resistance in the B-biotype of Bemisia tabaci (Hemiptera: Aleyrodidae) is associated with a point mutation in an ace1-type acetylcholinesterase and overexpression of carboxylesterase
inferredcites →https://doi.org/10.1016/j.ibmb.2014.05.003openalex-snapshot
The evolution of insecticide resistance in the peach potato aphid, Myzus persicae
inferredcites →https://doi.org/10.1016/j.ibmb.2016.06.002openalex-snapshot
Reduced abundance of the CYP6CY3-targeting let-7 and miR-100 miRNAs accounts for host adaptation of Myzus persicae nicotianae
inferredcites →https://doi.org/10.1016/j.ibmb.2019.04.016openalex-snapshot
An integrated protocol for targeted mutagenesis with CRISPR-Cas9 system in the pea aphid
inferredcites →https://doi.org/10.1016/j.mcp.2019.07.001openalex-snapshot
SATQPCR: Website for statistical analysis of real-time quantitative PCR data
inferredcites →https://doi.org/10.1016/j.pestbp.2009.07.010openalex-snapshot
A review of the interactions between multiple insecticide resistance loci
inferredcites →https://doi.org/10.1016/j.pestbp.2013.08.005openalex-snapshot
Investigating nicotinic acetylcholine receptor expression in neonicotinoid resistant Myzus persicae FRC
inferredcites →https://doi.org/10.1016/j.pestbp.2015.04.004openalex-snapshot
The global status of insect resistance to neonicotinoid insecticides
inferredcites →https://doi.org/10.1016/j.pestbp.2015.11.008openalex-snapshot
Insecticide resistance monitoring and metabolic mechanism study of the green peach aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae), in Chongqing, China
inferredcites →https://doi.org/10.1016/j.pestbp.2016.11.004openalex-snapshot
Both point mutations and low expression levels of the nicotinic acetylcholine receptor β1 subunit are associated with imidacloprid resistance in an Aphis gossypii (Glover) population from a Bt cotton field in China
inferredcites →https://doi.org/10.1016/j.pestbp.2019.06.002openalex-snapshot
UDP-glucosyltransferases potentially contribute to imidacloprid resistance in Aphis gossypii glover based on transcriptomic and proteomic analyses
inferredcites →https://doi.org/10.1016/j.pestbp.2019.07.011openalex-snapshot
CYP-mediated resistance and cross-resistance to pyrethroids and organophosphates in Aedes aegypti in the presence and absence of kdr
inferredcites →https://doi.org/10.1016/j.pestbp.2020.104595openalex-snapshot
Using CRISPR/Cas9 genome modification to understand the genetic basis of insecticide resistance: Drosophila and beyond
inferredcites →https://doi.org/10.1016/j.tplants.2016.06.006openalex-snapshot
Trends and Challenges in Pesticide Resistance Detection
inferredcites →https://doi.org/10.1017/chol9780521077910openalex-snapshot
The Cambridge Ancient History
inferredcites →https://doi.org/10.1017/s0007485300047830openalex-snapshot
Life-cycle variation of Myzus persicae (Sulz.) (Hom., Aphididae) in different parts of the world, in relation to genotype and environment
inferredcites →https://doi.org/10.1017/s0007485307005524openalex-snapshot
Characterization of the M918T sodium channel gene mutation associated with strong resistance to pyrethroid insecticides in the peach-potato aphid,Myzus persicae(Sulzer)
inferredcites →https://doi.org/10.1038/s42003-021-02373-xopenalex-snapshot
Global patterns in genomic diversity underpinning the evolution of insecticide resistance in the aphid crop pest Myzus persicae
inferredcites →https://doi.org/10.1046/j.1365-2583.1999.83121.xopenalex-snapshot
A sodium channel point mutation is associated with resistance to DDT and pyrethroid insecticides in the peach‐potato aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae)
inferredcites →https://doi.org/10.1073/pnas.1314122110openalex-snapshot
Gene amplification and microsatellite polymorphism underlie a recent insect host shift
inferredcites →https://doi.org/10.1073/pnas.2100559118openalex-snapshot
Transposon-mediated insertional mutagenesis unmasks recessive insecticide resistance in the aphid Myzus persicae
inferredcites →https://doi.org/10.1079/9781845933531.0000openalex-snapshot
Global pesticide resistance in arthropods
inferredcites →https://doi.org/10.1080/096708798228275openalex-snapshot
A revolving dose strategy to delay the evolution of both quantitative vs major monogene resistances to pesticides and drugs
inferredcites →https://doi.org/10.1093/jee/tow148openalex-snapshot
Assessment of the Dominance Level of the R81T Target Resistance to Two Neonicotinoid Insecticides inMyzus persicae(Hemiptera: Aphididae)
inferredcites →https://doi.org/10.1098/rspb.2020.0838openalex-snapshot
‘What I cannot create, I do not understand’: functionally validated synergism of metabolic and target site insecticide resistance
inferredcites →https://doi.org/10.1111/1744-7917.12310openalex-snapshot
Evaluation of the reference genes for expression analysis using quantitative real‐time polymerase chain reaction in the green peach aphid, Myzus persicae
inferredcites →https://doi.org/10.1111/brv.12440openalex-snapshot
The evolutionary origins of pesticide resistance
inferredcites →https://doi.org/10.1111/eva.13417openalex-snapshot
Host plants and insecticides shape the evolution of genetic and clonal diversity in a major aphid crop pest
inferredcites →https://doi.org/10.1111/j.0962-1075.2004.00513.xopenalex-snapshot
Two amino acid substitutions in acetylcholinesterase associated with pirimicarb and organophosphorous insecticide resistance in the cotton aphid, Aphis gossypii Glover (Homoptera: Aphididae)
inferredcites →https://doi.org/10.1111/j.1420-9101.2008.01661.xopenalex-snapshot
Multiplicative interaction between the two major mechanisms of permethrin resistance, kdr and cytochrome P450‐monooxygenase detoxification, in mosquitoes
inferredcites →https://doi.org/10.1111/j.1570-7458.1993.tb01663.xopenalex-snapshot
Protein toxicity to aphids: an in vitro test on Acyrthosiphon pisum
inferredcites →https://doi.org/10.1111/j.1744-7917.2010.01387.xopenalex-snapshot
Insecticide resistance in Bemisia tabaci from Cyprus
inferredcites →https://doi.org/10.1111/mec.12170openalex-snapshot
The impact of transposable elements in environmental adaptation
inferredcites →https://doi.org/10.1111/mec.15503openalex-snapshot
Evolutionary trade‐offs of insecticide resistance — The fitness costs associated with target‐site mutations in the nAChR of Drosophila melanogaster
inferredcites →https://doi.org/10.1126/sciadv.aba1070openalex-snapshot
The genetic architecture of a host shift: An adaptive walk protected an aphid and its endosymbiont from plant chemical defenses
inferredcites →https://doi.org/10.1126/science.aaa2721openalex-snapshot
What I cannot create, I do not understand
inferredcites →https://doi.org/10.1146/annurev-ento-070621-061328openalex-snapshot
The Role of Cytochrome P450s in Insect Toxicology and Resistance
inferredcites →https://doi.org/10.1146/annurev-ento-070720-074650openalex-snapshot
Transposable Elements and the Evolution of Insects
inferredcites →https://doi.org/10.1186/1471-2202-12-51openalex-snapshot
Mutation of a nicotinic acetylcholine receptor β subunit is associated with resistance to neonicotinoid insecticides in the aphid Myzus persicae
inferredcites →https://doi.org/10.1371/journal.pgen.1000999openalex-snapshot
Amplification of a Cytochrome P450 Gene Is Associated with Resistance to Neonicotinoid Insecticides in the Aphid Myzus persicae
inferredcites →https://doi.org/10.1371/journal.pgen.1009556openalex-snapshot
CRISPR/Cas9 modified An. gambiae carrying kdr mutation L1014F functionally validate its contribution in insecticide resistance and combined effect with metabolic enzymes
inferredcites →https://doi.org/10.1371/journal.pgen.1009680openalex-snapshot
Genome mapping coupled with CRISPR gene editing reveals a P450 gene confers avermectin resistance in the beet armyworm
inferredcites →https://doi.org/10.1371/journal.pntd.0005625openalex-snapshot
Contemporary status of insecticide resistance in the major Aedes vectors of arboviruses infecting humans
inferredcites →https://doi.org/10.1371/journal.pone.0036810openalex-snapshot
Insecticide Resistance Mechanisms in the Green Peach Aphid Myzus persicae (Hemiptera: Aphididae) II: Costs and Benefits
inferredcites →https://doi.org/10.1371/journal.pone.0146021openalex-snapshot
Dose-Response Analysis Using R
inferredcites →https://doi.org/10.1371/journal.pone.0154633openalex-snapshot
Molecular Cloning, Expression Pattern and Polymorphisms of NADPH-Cytochrome P450 Reductase in the Bird Cherry-Oat Aphid Rhopalosiphum padi (L.)
inferredcites →https://doi.org/10.1584/jpestics.d14-031openalex-snapshot
The cross-resistance patterns and biochemical characteristics of an imidacloprid-resistant strain of the cotton aphid
inferredcites →https://doi.org/10.1584/jpestics.d19-017openalex-snapshot
Differential metabolism of neonicotinoids by Myzus persicae CYP6CY3 stably expressed in Drosophila S2 cells
inferredcites →https://doi.org/10.1603/0022-0493-93.6.1588openalex-snapshot
Insecticide Resistance and Dominance Levels
inferredcites →https://doi.org/10.1673/031.006.3801openalex-snapshot
RNAi Knockdown of a Salivary Transcript Leading to Lethality in the Pea Aphid, Acyrthosiphon pisum
inferredcites →https://doi.org/10.17605/osf.io/byv62openalex-snapshot
Resistance cases to PPPs in France / Cas de résistance aux PPP en France
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ps.70888openalex-snapshot
Nanoparticle‐enhanced multi‐target RNAi in Myzus persicae : Molecular mechanisms, cross‐kingdom sRNA transfer, and efficacy for sustainable pest management
inferred← citeshttps://doi.org/10.1002/ps.71361openalex-snapshot
Comparative genomic analysis of P450 genes reveals CYP6CX4 is associated with differential clothianidin resistance between Bemisia tabaci B/ MEAM1 and Q/ MED
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2026.108990openalex-snapshot
Incorporation of powerful RNA interference targets within nano-enabled co-delivery platforms for broad-spectrum resistance management
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.113183openalex-snapshot
Carbene–catalyzed mesoionization via formal [3+2] cycloaddition for mesoionic insecticide discovery
inferred← citeshttps://doi.org/10.1016/j.cpb.2026.100652openalex-snapshot
Integrated phenotypic, physio-biochemical, and metabolomic dissection reveals defense mechanisms of Brassica napus against aphid infestation
inferred← citeshttps://doi.org/10.1016/j.cropro.2025.107434openalex-snapshot
Peppermint interplanting and nitrogen fertilisation for green peach aphid management in peach orchards: Field evidence of VOC-mediated effects
inferred← citeshttps://doi.org/10.1016/j.cropro.2026.107871openalex-snapshot
Pest management in potato: crop physiology, thresholds, and decision support for sustainable crop protection
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.126190openalex-snapshot
Emission of CO2 enhanced by thiamethoxam and cadmium in agricultural soil
inferred← citeshttps://doi.org/10.1016/j.ibmb.2026.104487openalex-snapshot
The cytochrome P450s CYP6CY3 and CYP6CY4 confer resistance to flupyradifurone in the green peach aphid Myzus persicae
inferred← citeshttps://doi.org/10.1016/j.pestbp.2024.106205openalex-snapshot
Field-evolved resistance to neonicotinoids in the mosquito, Anopheles gambiae, is associated with mutations of nicotinic acetylcholine receptor subunits combined with cytochrome P450-mediated detoxification
inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106816openalex-snapshot
An in silico pipeline for enzyme-substrate modelling using arthropod P450s
inferred← citeshttps://doi.org/10.1016/j.pestbp.2026.107049openalex-snapshot
Biochemical and genetic mechanisms of resistance in Myzus persicae: A major challenge for global crop protection
inferred← citeshttps://doi.org/10.1016/j.pestbp.2026.107338openalex-snapshot
Mechanisms of first- to fourth-generation neonicotinoid resistance in Myzus persicae from Beijing peach orchards: Roles of target-site mutations and detoxification metabolism
inferred← citeshttps://doi.org/10.1021/acsomega.5c02740openalex-snapshot
New Mesoionic Pyrido[1,2-a] Pyrimidines Containing Oxime Esters against Megoura japonica with Better Safety to Pollinating Insects
inferred← citeshttps://doi.org/10.1111/eea.70178openalex-snapshot
Cuticular Protein CP19a is Essential for the Response of Peach Aphid Myzus persicae (Sulzer) to UV ‐B Stress
inferred← citeshttps://doi.org/10.1186/s12951-026-04172-0openalex-snapshot
Coupled mesoporous silica nanoparticles and limonene–chitosan Pickering emulsions: enhanced insecticidal delivery and selectivity
inferred← citeshttps://doi.org/10.16970/entoted.1572732openalex-snapshot
Effect of Trichoderma harzianum Rifai and Trichoderma viride Pers. (Ascomycota: Hypocreales) on demographic parameters of Myzus persicae (Sulzer, 1776) (Hemiptera: Aphididae) feeding on bell pepper plant
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7480243/v1openalex-snapshot
Nanoparticle-enhanced multi-target RNAi in Myzus persicae: molecular mechanisms, cross-kingdom sRNA transfer, and efficacy for sustainable pest management
inferred← citeshttps://doi.org/10.2139/ssrn.5354412openalex-snapshot
The P450s Cyp6cy3 and Cyp6cy4 Confer Resistance to Flupyradifurone in the Green Peach Aphid Myzus Persicae
inferred← citeshttps://doi.org/10.3389/finsc.2026.1853500openalex-snapshot
Soil nutrition and foliar intervention in Brassica napus (L.) to impair biological fitness of green peach aphid (Myzus persicae Sulzer)
inferred← citeshttps://doi.org/10.3390/agronomy15020280openalex-snapshot
Evaluation of Insecticide Toxicity and Field Performance Against Myzus persicae (Hemiptera: Aphididae) in Laboratory and Greenhouse Conditions
inferred← citeshttps://doi.org/10.3390/toxics13080681openalex-snapshot
Mechanisms and Genetic Drivers of Resistance of Insect Pests to Insecticides and Approaches to Its Control
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