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Insecticide resistance traits differ among and within host races in Aphis gossypii
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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/(sici)1096-9063(199701)49:1<90::aid-ps489>3.0.co;2-sopenalex-snapshot
Communication to the Editor Insecticide Resistance in a Strain ofAphis gossypiifrom Southern France
inferredcites →https://doi.org/10.1002/arch.20049openalex-snapshot
Glutathione S-transferases in the adaptation to plant secondary metabolites in theMyzus persicae aphid
inferredcites →https://doi.org/10.1002/ps.1807openalex-snapshot
Esterase‐mediated resistance to pyrethroids in field populations of Helicoverpa armigera (Lepidoptera: Noctuidae) from Central Africa
inferredcites →https://doi.org/10.1002/ps.2780350202openalex-snapshot
Insecticide resistance in cotton aphid Aphis gossypii (Glov.) in the Sudan Gezira
inferredcites →https://doi.org/10.1002/ps.2780430104openalex-snapshot
A biochemical mechanism of resistance to pirimicarb in two glasshouse clones of Aphis gossypii
inferredcites →https://doi.org/10.1002/ps.971openalex-snapshot
Biochemical evidence that an S431F mutation in acetylcholinesterase‐1 of Aphis gossypii mediates resistance to pirimicarb and omethoate
inferredcites →https://doi.org/10.1006/pest.1996.0004openalex-snapshot
Esterases and Esfenvalerate Resistance in AustralianHelicoverpa armigera(Hübner) Lepidoptera:Noctuidae
inferredcites →https://doi.org/10.1006/pest.1996.0064openalex-snapshot
Characterisation of Insensitive Acetylcholinesterase in Insecticide-Resistant Cotton Aphids,Aphis gossypiiGlover (Homoptera: Aphididae)
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/10.1016/0261-2194(85)90044-4openalex-snapshot
Aphids on the World's crops: An identification and information guide
inferredcites →https://doi.org/10.1016/j.cropro.2007.08.006openalex-snapshot
Susceptibility of Pakistani populations of cotton aphid Aphis gossypii (Homoptera: Aphididae) to endosulfan, organophosphorus and carbamate insecticides
inferredcites →https://doi.org/10.1016/j.pestbp.2006.07.009openalex-snapshot
Resistance mechanisms and associated mutations in acetylcholinesterase genes in Sitobion avenae (Fabricius)
inferredcites →https://doi.org/10.1016/j.pestbp.2007.11.004openalex-snapshot
Overexpression of carboxylesterase gene associated with organophosphorous insecticide resistance in cotton aphids, Aphis gossypii (Glover)
inferredcites →https://doi.org/10.1017/s0007485307005585openalex-snapshot
Genotypic diversity of the cotton-melon aphidAphis gossypii(Glover) in Tunisia is structured by host plants
inferredcites →https://doi.org/10.1017/s0021859600078692openalex-snapshot
Some properties of l-chloro-2,4-dinitrochlorobenzene linked glutathione S-transferase in dichlorvos resistant and susceptible strains of cotton aphid (Homoptera: Aphididae)
inferredcites →https://doi.org/10.1023/a:1026481524896openalex-snapshot
Effect of Two Wheat Cultivars Differing in Hydroxamic Acid Concentration on Detoxification Metabolism in the AphidSitobion avenae
inferredcites →https://doi.org/10.1046/j.1365-2311.1999.00223.xopenalex-snapshot
Inter‐strain competition and dispersal in aphids: evidence from a greenhouse study
inferredcites →https://doi.org/10.1046/j.1365-294x.1997.00179.xopenalex-snapshot
Genetic variation in an introduced aphid pest (Metopolophium dirhodum) in New Zealand and relation to individuals from europe
inferredcites →https://doi.org/10.1046/j.1365-294x.1998.00421.xopenalex-snapshot
Host‐based genetic differentiation in the aphid Aphis gossypii Glover, evidenced from RAPD fingerprints
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00782.xopenalex-snapshot
Variation in clonal diversity in glasshouse infestations of the aphid, Aphis gossypii Glover in southern France
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01998.xopenalex-snapshot
Environmentally related patterns of reproductive modes in the aphid Myzus persicae and the predominance of two ‘superclones’ in Victoria, Australia
inferredcites →https://doi.org/10.1046/j.1440-6055.2000.00134.xopenalex-snapshot
Baseline studies and preliminary resistance survey of Australian populations of cotton aphid Aphis gossypii Glover (Hemiptera: Aphididae)
inferredcites →https://doi.org/10.1046/j.1440-6055.2001.00200.xopenalex-snapshot
Insecticide resistance in Aphis gossypii Glover (Hemiptera: Aphididae), a serious threat to Australian cotton
inferredcites →https://doi.org/10.1080/15216540701352042openalex-snapshot
DDT, pyrethrins, pyrethroids and insect sodium channels
inferredcites →https://doi.org/10.1093/jee/21.5.715openalex-snapshot
Studies on the Resistance of Certain Insects to Hydrocyanic Acid
inferredcites →https://doi.org/10.1093/jee/85.3.651openalex-snapshot
Relationship of Insecticide Resistance to Carboxylesterases In Aphis gossypii (Homoptera: Aphididae) from Midsouth Cotton
inferredcites →https://doi.org/10.1093/jee/87.2.293openalex-snapshot
Resistance of Aphis gossypii (Homoptera: Aphididae) to Insecticides in Hawaii: Spatial Patterns and Relation to Insecticide Use
inferredcites →https://doi.org/10.1093/jee/89.2.302openalex-snapshot
Polyacrylamide Gel Electrophoretic Assessments of Esterases in Cotton Aphid (Homoptera: Aphididae) Resistance to Dichlorvos
inferredcites →https://doi.org/10.1093/jee/96.3.875openalex-snapshot
High Resistance of Field Populations of the Cotton Aphid Aphis gossypii Glover (Homoptera: Aphididae) to Pyrethroid Insecticides in Pakistan
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.0962-1075.2004.00517.xopenalex-snapshot
Identification of mutations conferring insecticide‐insensitive AChE in the cotton‐melon aphid, Aphis gossypii Glover
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00733.xopenalex-snapshot
A comparative study of voltage‐gated sodium channels in the Insecta: implications for pyrethroid resistance in Anopheline and other Neopteran species
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04190.xopenalex-snapshot
Ecological specialization of the aphid Aphis gossypii Glover on cultivated host plants
inferredcites →https://doi.org/10.1111/j.1365-3059.1980.tb01211.xopenalex-snapshot
Pirimicarb resistance in the melon and cotton aphid, Aphis gossypii Glover
inferredcites →https://doi.org/10.1111/j.1439-0418.1992.tb00636.xopenalex-snapshot
Resistance of cereals to aphids: The interaction between hydroxamic acids and glutathione S‐transferases in the grain aphid Sitobion avenae (F.) (Hom., Aphididae)
inferredcites →https://doi.org/10.1111/j.1461-9563.2008.00377.xopenalex-snapshot
Genetic diversity of the cotton aphid Aphis gossypii in the unstable environment of a cotton growing area
inferredcites →https://doi.org/10.1111/j.1744-7348.1993.tb04066.xopenalex-snapshot
Aspects of insecticide resistance in the melon and cotton aphid, Aphis gossypii (Hemiptera: Aphididae)
inferredcites →https://doi.org/10.1111/j.1744-7917.1994.tb00250.xopenalex-snapshot
INSECTICIDE RESISTANCE OF COTTON APHID IN NORTH CHINA
inferredcites →https://doi.org/10.1146/annurev.ento.51.110104.151104openalex-snapshot
Molecular Mechanisms of Metabolic Resistance to Synthetic and Natural Xenobiotics
inferredcites →https://doi.org/10.1303/aez.28.263openalex-snapshot
Insecticide Resistance of the Cotton Aphid, Aphis gossypii GLOVER(Homoptera:Aphididae) : VI. Qualitative Variations of Aliesterase Activity
inferredcites →https://doi.org/10.1303/aez.28.439openalex-snapshot
Carboxylesterase of the Cotton Aphid, Aphis gossypii GLOVER(Homoptera:Aphididae), Responsible for Fenitrothion Resistance as a Sequestering Protein
inferredcites →https://doi.org/10.1303/aez.29.300openalex-snapshot
Acetylcholinesterase of the Cotton Aphid, Aphis gossypii GLOVER (Homoptera: Aphididae) : I. Three Clone-Types Possessing Acetyl-cholinesterases of Low and High Sensitivity to Pirimicarb, and the Mixture
inferredcites →https://doi.org/10.1303/jjaez.33.204openalex-snapshot
Insecticide resistance of the cotton aphid, Aphis gossypii Glover (Homoptera: Aphididae). I. Susceptibility to several insecticides and esterase activity of field populations collected in Shizuoka Prefecture.
inferredcites →https://doi.org/10.1303/jjaez.36.101openalex-snapshot
Insecticide Resistance in Cotton Aphid, Aphis gossypii GLOVER(Homoptera: Aphididae) I. Aliesterase Activity and Organophosphorus-Susceptibility of Populations on Eggplants and Cucumbers.
inferredcites →https://doi.org/10.1303/jjaez.39.151openalex-snapshot
Insecticide Resistance in Clones of Cotton Aphid, Aphis gossypii GLOVER (Homoptera: Aphidiae), and Synergistic Effect of Esterase and Mixed-Function Oxidase Inhibitors.
inferredcites →https://doi.org/10.1584/jpestics.g06-51openalex-snapshot
Resistance of Aphis gossypii (Homoptera: Aphididae) to selected insecticides on cotton from five cotton production regions in Shandong, China
inferredcites →https://doi.org/10.1603/0013-8746(2008)101[565:dihplc]2.0.co;2openalex-snapshot
Differences in Host Preference, Life Cycle Pattern, and Insecticide Susceptibility Among Aphis gossypii Clones and Genetic Relationships Inferred from Internal Transcribed Spacer 2 Sequences of rDNA
inferredcites →https://doi.org/10.1603/0022-0493-98.4.1325openalex-snapshot
Polymorphisms in a Carboxylesterase Gene Between Organophosphate-Resistant and -Susceptible Aphis gossypii (Homoptera: Aphididae)
inferredcites →https://doi.org/10.18474/0749-8004-29.3.289openalex-snapshot
Susceptibility of Aphis gossypii (Glover) to Insecticides as Affected by Host Plant Using a Rapid Bioassay
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.4655308openalex-extracted
Life Parameters and Physiological Responses to Sublethal Concentrations of Afidopyropen in Cotton Aphid, Aphis Gossypii Glover
inferred← citeshttps://doi.org/10.1002/arch.70210openalex-snapshot
Delivery, Persistence, and Functional Response of dsRNA in Acyrthosiphon pisum : Progress and Remaining Barriers
inferred← citeshttps://doi.org/10.1002/ece3.4181openalex-snapshot
Genetic diversity of melon aphids Aphis gossypii associated with landscape features
inferred← citeshttps://doi.org/10.1002/mbo3.652openalex-snapshot
Bacterial communities in natural versus pesticide‐treated Aphis gossypii populations in North China
inferred← citeshttps://doi.org/10.1002/ps.2224openalex-snapshot
Uncommon associations in target resistance among French populations of Myzus persicae from oilseed rape crops
inferred← citeshttps://doi.org/10.1002/ps.3455openalex-snapshot
Evidence of superclones in Australian cotton aphid Aphis gossypii Glover (Aphididae: Hemiptera)
inferred← citeshttps://doi.org/10.1002/ps.4622openalex-snapshot
Pyrethroid resistance associated with M918 L mutation and detoxifying metabolism in Aphis gossypii from Bt cotton growing regions of China
inferred← citeshttps://doi.org/10.1002/ps.5039openalex-snapshot
Plant training for induced defense against insect pests: a promising tool for integrated pest management in cotton
inferred← citeshttps://doi.org/10.1002/ps.5081openalex-snapshot
The regulation of three new members of the cytochrome P450 CYP6 family and their promoters in the cotton aphid Aphis gossypii by plant allelochemicals
inferred← citeshttps://doi.org/10.1002/ps.5829openalex-snapshot
Super‐ kdr mutation M918L and multiple cytochrome P450s associated with the resistance of Rhopalosiphum padi to pyrethroid
inferred← citeshttps://doi.org/10.1002/ps.6385openalex-snapshot
Evaluation of sublethal and transgenerational effects of sulfoxaflor on Aphis gossypii via life table parameters and 16S rRNA sequencing
inferred← citeshttps://doi.org/10.1002/ps.6820openalex-snapshot
Evidence of enhanced reproductive performance and lack‐of‐fitness costs among soybean aphids, Aphis glycines, with varying levels of pyrethroid resistance
inferred← citeshttps://doi.org/10.1002/ps.70182openalex-snapshot
Adaptive divergence of three Aphis gossypii haplotypes on leguminous hosts
inferred← citeshttps://doi.org/10.1002/ps.70851openalex-snapshot
HvarAKR1B1 ‐mediated tolerance in Hippodamia variegata : Deciphering the metabolic adaptation and fitness costs under prolonged starvation
inferred← citeshttps://doi.org/10.1002/ps.71006openalex-snapshot
Mutations M918T , M918L , and L1014F impair pyrethroid binding and alter gating of the Megalurothrips usitatus sodium channel
inferred← citeshttps://doi.org/10.1002/ps.71178openalex-snapshot
The first report of M918L ( super‐kdr ) and L932F voltage‐gated sodium channel mutations in the English grain aphid ( Sitobion avenae )
inferred← citeshttps://doi.org/10.1002/ps.7220openalex-snapshot
Effects of transgenic cotton lines expressing dsAgCYP6CY3‐P1 on the growth and detoxification ability of Aphis gossypii glover
inferred← citeshttps://doi.org/10.1002/ps.7625openalex-snapshot
Effects of fungicides on fitness and Buchnera endosymbiont density in Aphis gossypii
inferred← citeshttps://doi.org/10.1002/ps.8142openalex-snapshot
Survey of target site mutations linked with insecticide resistance in Italian populations of Aphis gossypii
inferred← citeshttps://doi.org/10.1002/ps.8647openalex-snapshot
Response of Amblyseius swirskii to deltamethrin
inferred← citeshttps://doi.org/10.1002/ps.8771openalex-snapshot
Bacterial volatiles from aphid honeydew mediate ladybird beetles oviposition site choice
inferred← citeshttps://doi.org/10.1002/ps.8845openalex-snapshot
Genetic mutations and insecticide resistance in Diaphorina citri: a comparative study across Chinese citrus regions
inferred← citeshttps://doi.org/10.1007/698_2019_432openalex-snapshot
The Ecological and Evolutionary Implications of Pyrethroid Exposure: A New Perspective on Aquatic Ecotoxicity
inferred← citeshttps://doi.org/10.1007/978-3-030-38881-2_1openalex-snapshot
Crop Protection for Agricultural Intensification Systems in Sub-Saharan Africa
inferred← citeshttps://doi.org/10.1007/978-981-19-0343-4_14openalex-snapshot
Insecticide Resistance and Its Management in the Insect Pests of Horticultural Crops
inferred← citeshttps://doi.org/10.1007/s10340-015-0651-5openalex-snapshot
A TaqMan qPCR method for detecting kdr resistance in Aphis gossypii demonstrates improved sensitivity compared to conventional PCR–RFLP
inferred← citeshttps://doi.org/10.1007/s10340-018-1050-5openalex-snapshot
Multiple acaricide resistance and underlying mechanisms in Tetranychus urticae on hops
inferred← citeshttps://doi.org/10.1007/s10340-020-01321-8openalex-snapshot
Mutations associated with pyrethroid resistance in the honey bee parasite Varroa destructor evolved as a series of parallel and sequential events
inferred← citeshttps://doi.org/10.1007/s10493-020-00559-2openalex-snapshot
Physiological responses of plants and mites to salicylic acid improve the efficacy of spirodiclofen for controlling Tetranychus urticae (Acari: Tetranychidae) on greenhouse tomatoes
inferred← citeshttps://doi.org/10.1007/s10493-023-00879-zopenalex-snapshot
Geographical distribution of pyrethroid resistance mutations in Varroa destructor across Türkiye and a European overview
inferred← citeshttps://doi.org/10.1007/s10646-016-1732-9openalex-snapshot
Sublethal and transgenerational effects of sulfoxaflor on the biological traits of the cotton aphid, Aphis gossypii Glover (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1007/s10709-023-00181-1openalex-snapshot
Genome wide identification and evolutionary analysis of vat like NBS-LRR genes potentially associated with resistance to aphids in cotton
inferred← citeshttps://doi.org/10.1007/s11298-024-4031-4openalex-snapshot
Skabies: Eine ansteckende und belastende Hauterkrankung
inferred← citeshttps://doi.org/10.1007/s11356-021-15090-zopenalex-snapshot
Dimethoate induces genotoxicity as a result of oxidative stress: in vivo and in vitro studies
inferred← citeshttps://doi.org/10.1007/s11829-022-09944-7openalex-snapshot
Cotton topping reduces the performance of aphids on topped and neighbor plants under greenhouse conditions
inferred← citeshttps://doi.org/10.1007/s12600-019-00765-8openalex-snapshot
Biochemical resistance to insecticide in Bemisia tabaci field population from Burkina Faso, West Africa
inferred← citeshttps://doi.org/10.1007/s12600-026-01373-zopenalex-snapshot
Effect of Feeding Experience on the Host Adaptation of Three Aphis gossypii Haplotypes
inferred← citeshttps://doi.org/10.1007/s13355-025-00916-wopenalex-snapshot
Sodium channel mutations (M918L and L925V/M) in phytoseiid mite species and their distribution in apple orchards
inferred← citeshttps://doi.org/10.1007/s13593-014-0216-7openalex-snapshot
Pesticide risks from fruit and vegetable pest management by small farmers in sub-Saharan Africa. A review
inferred← citeshttps://doi.org/10.1007/s13593-017-0460-8openalex-snapshot
Protected cultivation of vegetable crops in sub-Saharan Africa: limits and prospects for smallholders. A review
inferred← citeshttps://doi.org/10.1007/s42452-019-1485-1openalex-snapshot
Worldwide pesticide usage and its impacts on ecosystem
inferred← citeshttps://doi.org/10.1016/b978-0-12-824315-2.00416-4openalex-snapshot
Pesticides and its toxicity
inferred← citeshttps://doi.org/10.1016/j.actatropica.2013.06.004openalex-snapshot
Insecticide resistance in Bemisia tabaci Gennadius (Homoptera: Aleyrodidae) and Anopheles gambiae Giles (Diptera: Culicidae) could compromise the sustainability of malaria vector control strategies in West Africa
inferred← citeshttps://doi.org/10.1016/j.actatropica.2026.108270openalex-snapshot
Primer design for the voltage-gated sodium channel, the pyrethroids’ target site, in the triatomine vector Triatoma infestans (Hemiptera: Reduviidae)
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Implications of cyantraniliprole sublethal doses on the population dynamics and gene expression of Aphis gossypii Glover (Hemiptera: Aphididae)
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Binary collaboration of carboxyl‐functionalized mesoporous silica microspheres and sliver nanoparticle improved imidacloprid bioactivity towards insecticide-resistance insect pests
inferred← citeshttps://doi.org/10.1016/j.cropro.2015.09.003openalex-snapshot
Cost:Benefit analysis of insect net use in cabbage in real farming conditions among smallholder farmers in Benin
inferred← citeshttps://doi.org/10.1016/j.cropro.2022.106153openalex-snapshot
First report of the kdr pyrethroid resistance mutation in a French population of the English grain aphid, Sitobion avenae
inferred← citeshttps://doi.org/10.1016/j.cropro.2025.107426openalex-snapshot
Contamination by systemic insecticide harms the dispersal ability of the lady beetle Hippodamia variegata
inferred← citeshttps://doi.org/10.1016/j.crvi.2010.12.008openalex-snapshot
Biological invasions in agricultural settings: Insights from evolutionary biology and population genetics
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115203openalex-snapshot
Sublethal effects of acetamiprid and afidopyropen on Harmonia axyridis: insights from transcriptomics analysis
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.119210openalex-snapshot
Overexpression of multiple odorant binding and chemosensory protein genes contributed to multi-insecticide resistance in Aphis gossypii Glover
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120068openalex-snapshot
Sublethal imidacloprid exposure disrupts olfactory-mediated host location in Hippodamia variegata through transcriptional and functional impairment of olfactory genes
inferred← citeshttps://doi.org/10.1016/j.ibmb.2019.103285openalex-snapshot
Transcriptional responses of soybean aphids to sublethal insecticide exposure
inferred← citeshttps://doi.org/10.1016/j.ibmb.2023.103937openalex-snapshot
The molecular mechanisms of insecticide resistance in aphid crop pests
inferred← citeshttps://doi.org/10.1016/j.ibmb.2024.104214openalex-snapshot
A Unique Mechanism of Transfluthrin Action Revealed by Mapping its Binding Sites in the Mosquito Sodium Channel
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.128995openalex-snapshot
Identification and characterization of both cis- and trans-regulators mediating fenvalerate-induced expression of CYP6B7 in Helicoverpa armigera
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.139455openalex-snapshot
Role of mutation G255A in modulating pyrethroid sensitivity in insect sodium channels
inferred← citeshttps://doi.org/10.1016/j.indcrop.2017.08.034openalex-snapshot
Pesticidal plants in Africa: A global vision of new biological control products from local uses
inferred← citeshttps://doi.org/10.1016/j.jfca.2025.107975openalex-snapshot
Ozone treatment as a green technology for removing acetamiprid residues from some vegetables and its impact on the quality of vegetables
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133575openalex-snapshot
Uridine diphosphate glucosyltransferases are involved in spinosad resistance in western flower thrips Frankliniella occidentalis (Pergande)
inferred← citeshttps://doi.org/10.1016/j.pestbp.2013.02.007openalex-snapshot
Diversity and convergence of sodium channel mutations involved in resistance to pyrethroids
inferred← citeshttps://doi.org/10.1016/j.pestbp.2016.02.005openalex-snapshot
Cycloxaprid: A novel cis-nitromethylene neonicotinoid insecticide to control imidacloprid-resistant cotton aphid (Aphis gossypii)
inferred← citeshttps://doi.org/10.1016/j.pestbp.2019.04.012openalex-snapshot
T929I and K1774N mutation pair and M918L single mutation identified in the voltage-gated sodium channel gene of pyrethroid-resistant Thrips tabaci (Thysanoptera: Thripidae) in Japan
inferred← citeshttps://doi.org/10.1016/j.pestbp.2022.105060openalex-snapshot
Identification of cis-acting elements in response to fenvalerate in the CYP6B7 promoter of Helicoverpa armigera
inferred← citeshttps://doi.org/10.1016/j.pestbp.2022.105078openalex-snapshot
Toxicological assessment of sublethal dose of acetamiprid in male mice and the efficacy of quercetin
inferred← citeshttps://doi.org/10.1016/j.pestbp.2026.107303openalex-snapshot
Development of an RPA-CRISPR/Cas12a-based rapid visual detection method for two insecticide resistance-associated mutations in Aphis gossypii: A302S in the ace1 gene and M918L in the para gene
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.171984openalex-snapshot
Mesoporous silica nanospheres-mediated insecticide and antibiotics co-delivery system for synergizing insecticidal toxicity and reducing environmental risk of insecticide
inferred← citeshttps://doi.org/10.1016/j.vprsr.2024.101121openalex-snapshot
Detection of mutations in the voltage-gated sodium channel gene of Varroa destructor (Acari: Varroidae) populations
inferred← citeshttps://doi.org/10.1017/s0007485310000635openalex-snapshot
Insecticide use and competition shape the genetic diversity of the aphid Aphis gossypii in a cotton-growing landscape
inferred← citeshttps://doi.org/10.1017/s0007485326101175openalex-snapshot
Molecular monitoring of insecticide resistance in Aphis gossypii Glover (Hemiptera: Aphididae) from different crops in Greece, using novel ddPCR diagnostics
inferred← citeshttps://doi.org/10.1017/s0014479720000186openalex-snapshot
Mitigation of climatic conditions and pest protection provided by insect-proof nets for cabbage cultivation in East Africa
inferred← citeshttps://doi.org/10.1038/s41598-024-54443-9openalex-snapshot
Evolutionary origin and distribution of amino acid mutations associated with resistance to sodium channel modulators in onion thrips, Thrips tabaci
inferred← citeshttps://doi.org/10.1038/srep30166openalex-snapshot
Expression patterns, mutation detection and RNA interference of Rhopalosiphum padi voltage-gated sodium channel genes
inferred← citeshttps://doi.org/10.1073/pnas.1302023110openalex-snapshot
Multiple origins of pyrethroid insecticide resistance across the species complex of a nontarget aquatic crustacean, Hyalella azteca
inferred← citeshttps://doi.org/10.1080/09583157.2015.1099148openalex-snapshot
Interactions among vegetable-infesting aphids, the fungal pathogenMetarhizium anisopliae(Ascomycota: Hypocreales) and the predatory coccinellidCheilomenes lunata(Coleoptera: Coccinellidae)
inferred← citeshttps://doi.org/10.1080/09670874.2015.1095372openalex-snapshot
Relationship of phenotypic structures and allelochemical compounds of okra (Abelmoschusspp.) to resistance againstAphis gossypiiGlover
inferred← citeshttps://doi.org/10.1080/14620316.2019.1665481openalex-snapshot
Small mesh nets protect tomato plants from insect pests and increase yields in eastern Africa
inferred← citeshttps://doi.org/10.1093/jee/toaa202openalex-snapshot
Micronutrient Fertilization of Greenhouse Cucumbers Mitigates Pirimicarb Resistance in Aphis gossypii (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1093/jee/toab117openalex-snapshot
Pyrethroid Resistance and Fitness Cost Conferred by the super-kdr Mutation M918L in Rhopalosiphum padi (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1093/jee/toaf067openalex-snapshot
Molecular insights on the function of CYP380C12 in Aphis gossypii Glover (Hemiptera: Aphididae): in silico and RNAi analyses
inferred← citeshttps://doi.org/10.1093/jee/tov403openalex-snapshot
Multiple Mutations on the Second Acetylcholinesterase Gene Associated With Dimethoate Resistance in the Melon Aphid, Aphis gossypii (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1093/jee/tow322openalex-snapshot
Transcriptional responses of detoxification genes to four plant allelochemicals in Aphis gossypii
inferred← citeshttps://doi.org/10.1093/jee/tox311openalex-snapshot
Cry1 Bt Susceptibilities of Fall Armyworm (Lepidoptera: Noctuidae) Host Strains
inferred← citeshttps://doi.org/10.1093/jee/toy381openalex-snapshot
Toxicity and Sublethal Effects of Flupyradifurone, a Novel Butenolide Insecticide, on the Development and Fecundity ofAphis gossypii(Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1093/jee/toz021openalex-snapshot
Characterization of the Cytochrome P450 Gene CYP305A1 of the Cotton Aphid (Hemiptera: Aphididae) and Its Responsive Cis-Elements to Plant Allelochemicals
inferred← citeshttps://doi.org/10.1101/2021.09.03.458899openalex-snapshot
Experimental evolution of insect resistance to two pesticide classes reveals mechanistic diversity and context-dependent fitness costs
inferred← citeshttps://doi.org/10.1111/1744-7917.12288openalex-snapshot
Characterization of the voltage‐gated sodium channel of the Asian citrus psyllid, Diaphorina citri
inferred← citeshttps://doi.org/10.1111/eea.13093openalex-snapshot
Host‐associated differentiation of target pests should be assessed before using gene drive as a pest control tool − an opinion
inferred← citeshttps://doi.org/10.1111/eva.12382openalex-snapshot
Insight into the durability of plant resistance to aphids from a demo‐genetic study of Aphis gossypii in melon crops
inferred← citeshttps://doi.org/10.1111/imb.12642openalex-snapshot
Mutations in the voltage‐gated sodium channel gene associated with deltamethrin resistance in commercially sourced Phytoseiulus persimilis
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05242.xopenalex-snapshot
Climate effects on life cycle variation and population genetic architecture of the black bean aphid, Aphis fabae
inferred← citeshttps://doi.org/10.1111/jdv.19288openalex-snapshot
Detection of a knockdown mutation in the voltage‐sensitive sodium channel associated with permethrin tolerance in Sarcoptes scabiei var. hominis mites
inferred← citeshttps://doi.org/10.1111/jen.12848openalex-snapshot
First report of voltage‐gated sodium channel M918V and molecular diagnostics of nicotinic acetylcholine receptor R81T in the cotton aphid
inferred← citeshttps://doi.org/10.1186/1471-2148-12-47openalex-snapshot
What do spring migrants reveal about sex and host selection in the melon aphid?
inferred← citeshttps://doi.org/10.1186/s12951-024-02819-4openalex-snapshot
Nanoparticle LDH enhances RNAi efficiency of dsRNA in piercing-sucking pests by promoting dsRNA stability and transport in plants
inferred← citeshttps://doi.org/10.1371/journal.pone.0021263openalex-snapshot
Weak Spatial and Temporal Population Genetic Structure in the Rosy Apple Aphid, Dysaphis plantaginea, in French Apple Orchards
inferred← citeshttps://doi.org/10.1371/journal.pone.0261545openalex-snapshot
Virtual screening, molecular dynamics and binding energy-MM-PBSA studies of natural compounds to identify potential EcR inhibitors against Bemisia tabaci Gennadius
inferred← citeshttps://doi.org/10.14411/eje.2022.001openalex-snapshot
Inoculation of cucumber plants with Beauveria bassiana enhances resistance to Aphis gossypii (Hemiptera: Aphididae) and increases aphid susceptibility to pirimicarb
inferred← citeshttps://doi.org/10.1584/jpestics.d11-017openalex-snapshot
Detection of kdr pyrethroid resistance in the cotton aphid, Aphis gossypii (Hemiptera: Aphididae), using a PCR-RFLP assay
inferred← citeshttps://doi.org/10.1584/jpestics.d25-077openalex-snapshot
Distribution of sodium channel mutations associated with pyrethroid resistance in phytoseiid mite species in vineyards
inferred← citeshttps://doi.org/10.1584/jpestics.r10-10openalex-snapshot
Insecticide resistance through mutations in cholinesterases or carboxylesterases: data mining in the ESTHER database
inferred← citeshttps://doi.org/10.16970/entoted.1344982openalex-snapshot
Insecticide resistance of Aphis gossypii Glover, 1877 (Hemiptera: Aphididae) in cotton fields in Çukurova Region of Türkiye
inferred← citeshttps://doi.org/10.17660/actahortic.2015.1105.31openalex-snapshot
Eco-friendly nets to improve vegetable production and quality in sub-Saharan Africa
inferred← citeshttps://doi.org/10.17660/actahortic.2018.1225.5openalex-snapshot
Insect net: a novel technology to promote integrated pest management on horticultural crops in Africa
inferred← citeshttps://doi.org/10.17660/actahortic.2020.1294.24openalex-snapshot
Epidemiology of zucchini viruses in Flanders in support of a sustainable management strategy
inferred← citeshttps://doi.org/10.17816/ecogen677341openalex-snapshot
Molecular genetic patterns of pyrethroid resistance in diamondback moth (Plutella xylostella; Linnaeus, 1758)
inferred← citeshttps://doi.org/10.18475/cjos.v54i1.a1openalex-snapshot
An Assessment of Host Preference of Aphis gossypii Glover, 1877 (Hemiptera) in Jamaica
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1739929/v1openalex-snapshot
Comparative study on growth, physiological and biotic stress resistance of cucumber (Cucumis sativus L.) by exogenous application of jasmonic acid and methyl jasmonate under greenhouse conditions
inferred← citeshttps://doi.org/10.2139/ssrn.6920423openalex-snapshot
Development of a RPA-CRISPR/Cas12a-Based Visual Rapid Detection technique for Ala-302-Ser Mutation in ace2 confers Organophosphate Resistance and Met-918-Leu Mutation in para confers Pyrethroid Resisitance in Aphis gossypii
inferred← citeshttps://doi.org/10.3390/agriculture13122251openalex-snapshot
Development of Ethyl Formate Disinfestation Treatment Methods for the Prevention of the Introduction and Establishment of Exotic Insect Pests in Greenhouse Cultivation
inferred← citeshttps://doi.org/10.3390/agriculture16010083openalex-snapshot
Association of VGSC Mutations and P450 Overexpression with Beta-Cypermethrin Resistance in Aphis gossypii Glover from a Chinese Wolfberry (Lycium barbarum L.) Field
inferred← citeshttps://doi.org/10.3390/agronomy10091313openalex-snapshot
Effects of Sublethal Doses of Methyl Benzoate on the Life History Traits and Acetylcholinesterase (AChE) Activity of Aphis gossypii
inferred← citeshttps://doi.org/10.3390/agronomy13051245openalex-snapshot
Host-Plant Switching Impacts Susceptibility and Biochemical Responses of Cnaphalocrocis medinalis to Abamectin and Chlorpyrifos
inferred← citeshttps://doi.org/10.3390/agronomy14020258openalex-snapshot
Life Parameters and Physiological Reactions of Cotton Aphids Aphis gossypii (Hemiptera: Aphididae) to Sublethal Concentrations of Afidopyropen
inferred← citeshttps://doi.org/10.3390/genes15091124openalex-snapshot
Antioxidant Enzyme, Transcriptomic, and Metabolomic Changes in Lily (Lilium spp.) Leaves Induced by Aphis gossypii Glover
inferred← citeshttps://doi.org/10.3390/ijms24076750openalex-snapshot
Insights into the Effects of Insecticides on Aphids (Hemiptera: Aphididae): Resistance Mechanisms and Molecular Basis
inferred← citeshttps://doi.org/10.3390/insects12010032openalex-snapshot
Potential of Cucurbitacin B and Epigallocatechin Gallate as Biopesticides against Aphis gossypii
inferred← citeshttps://doi.org/10.3390/insects12080681openalex-snapshot
Transgenerational Effects of a Neonicotinoid and a Novel Sulfoximine Insecticide on the Harlequin Ladybird
inferred← citeshttps://doi.org/10.3390/insects13080745openalex-snapshot
Pyrethroids in an AlphaFold2 Model of the Insect Sodium Channel
inferred← citeshttps://doi.org/10.3390/insects15030173openalex-snapshot
Intergenerational Effects of Sublethal Lambda-Cyhalothrin Exposure on Aphis gossypii Glover (Hemiptera: Aphididae) Reproduction and Development
inferred← citeshttps://doi.org/10.3390/insects15040247openalex-snapshot
Sublethal Effects of Spirotetramat, Cyantraniliprole, and Pymetrozine on Aphis gossypii (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.3390/insects16010062openalex-snapshot
Effects of Temperature and Extraguild Prey Density on Intraguild Predation of Coccinella septempunctata and Harmonia axyridis
inferred← citeshttps://doi.org/10.3390/microorganisms10112242openalex-snapshot
Effects of Below-Ground Microbial Biostimulant Trichoderma harzianum on Diseases, Insect Community, and Plant Performance in Cucurbita pepo L. under Open Field Conditions
inferred← citeshttps://doi.org/10.3390/plants11243426openalex-snapshot
Rootstocks with Different Tolerance Grade to Citrus Tristeza Virus Induce Dissimilar Volatile Profile in Citrus sinensis and Avoidance Response in the Vector Aphis gossypii Glover
inferred← citeshttps://doi.org/10.3390/toxins14110750openalex-snapshot
Status of the Resistance of Aphis gossypii Glover, 1877 (Hemiptera: Aphididae) to Afidopyropen Originating from Microbial Secondary Metabolites in China
inferred← citeshttps://doi.org/10.4000/books.pur.149817openalex-snapshot
Filets imprégnés d’insecticides utilisés dans l’activité de maraîchage au Bénin : une innovation de santé par dérivation et par procuration
inferred← citeshttps://doi.org/10.4236/ae.2016.43018openalex-snapshot
Biochemical Characterization of Detoxifying Enzymes in Dimethoate-Resistant Strains of Melon Aphid, Aphis gossypii(Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.4314/acsj.v26i3.5openalex-snapshot
Galls of Guiera senegalensis J.F. GMEL (Combretaceae) as potential source of insecticides against the main cowpea pest Callosobruchus maculatus (Fab.) (Coleoptera: Bruchidae) detoxification enzymes
inferred← citeshttps://doi.org/10.55446/ije.2024.2465openalex-snapshot
Efficacy of Ethanolic Extract of Schanginia aegyptiaca and Artemisia herba-alba Against Aphid Aphis gossypii glover on Okra
inferred← citeshttps://doi.org/10.55446/ije.2025.3176openalex-snapshot
Status of Control of Hemipteran and Coleopteran Pests and Perspectives of Using Cuadb-Based Oligonucleotide Insecticides and RNA Biocontrols
inferred← citeshttps://doi.org/10.55507/gopzfd.1144369openalex-snapshot
Acetamiprid Resistance in the Green Peach Aphid Myzus persicae (Sulzer) (Hemiptera: Aphididae): Selection, Cross-Resistance, Biochemical and Molecular Resistance Mechanisms
inferred← citeshttps://doi.org/10.55730/1300-011x.3114openalex-snapshot
Neonicotinoid resistance in populations of the cotton aphid, Aphis gossypii Glover (Hemiptera: Aphididae) in Cotton Plantation Areas of Turkey
inferred← citeshttps://doi.org/10.70675/b3c6f456z9a3fz4d2bz8ce2zc49adc2fed34openalex-snapshot
Pressions de sélection exercées par les résistances génétiques du melon sur les populations d’Aphis gossypii
inferred← citeshttps://doi.org/10.70675/eba7b3ccz517dz48d6z9035zabcd081c1f6bopenalex-snapshot
Acquisition d’une tolérance aux insecticides en vergers de pommiers et ses conséquences chez une espèce auxiliaire, le forficule Forficula auricularia L
inferred← citeshttps://doi.org/10.7585/kjps.2022.26.2.140openalex-snapshot
Analysis of Point Mutations Associated with Fenvalerate-and Imidacloprid-resistant Cotton Aphids, Aphis gossypii (Hemiptera: Aphididae) and Selection of Insecticides for Effective Control
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