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CYP450 core involvement in multiple resistance strains of Aedes aegypti from French Guiana highlighted by proteomics, molecular and biochemical studies

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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/pmic.201500189openalex-snapshot
Calibration plot for proteomics: A graphical tool to visually check the assumptions underlying FDR control in quantitative experiments
inferredcites →https://doi.org/10.1002/ps.5287openalex-snapshot
Co‐occurrence of V1016I and F1534C mutations in the voltage‐gated sodium channel and resistance to pyrethroids in Aedes aegypti (L.) from the Colombian Caribbean region
inferredcites →https://doi.org/10.1007/0-387-29362-0_23openalex-snapshot
limma: Linear Models for Microarray Data
inferredcites →https://doi.org/10.1007/s00204-011-0726-xopenalex-snapshot
Molecular mechanisms of pyrethroid insecticide neurotoxicity: recent advances
inferredcites →https://doi.org/10.1016/j.actatropica.2010.09.005openalex-snapshot
Characterization of insecticide resistance in Trinidadian strains of Aedes aegypti mosquitoes
inferredcites →https://doi.org/10.1016/j.cbi.2014.09.024openalex-snapshot
The aldo-keto reductases (AKRs): Overview
inferredcites →https://doi.org/10.1016/j.ibmb.2004.03.018openalex-snapshot
The molecular basis of insecticide resistance in mosquitoes
inferredcites →https://doi.org/10.1016/j.ibmb.2007.09.007openalex-snapshot
Genomic analysis of detoxification genes in the mosquito Aedes aegypti
inferredcites →https://doi.org/10.1016/j.ibmb.2008.08.007openalex-snapshot
P450 reductase and cytochrome b5 interactions with cytochrome P450: Effects on house fly CYP6A1 catalysis
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.pt.2010.08.004openalex-snapshot
Pyrethroid resistance in African anopheline mosquitoes: what are the implications for malaria control?
inferredcites →https://doi.org/10.1017/s0007485314000091openalex-snapshot
Increased production of mitochondrial reactive oxygen species and reduced adult life span in an insecticide-resistant strain ofAnopheles gambiae
inferredcites →https://doi.org/10.1021/pr101065jopenalex-snapshot
Andromeda: A Peptide Search Engine Integrated into the MaxQuant Environment
inferredcites →https://doi.org/10.1021/pr7006208openalex-snapshot
Mapping the Larval Midgut Lumen Proteome of Helicoverpa armigera , a Generalist Herbivorous Insect
inferredcites →https://doi.org/10.1038/nbt.1511openalex-snapshot
MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
inferredcites →https://doi.org/10.1038/nbt.2839openalex-snapshot
ProteomeXchange provides globally coordinated proteomics data submission and dissemination
inferredcites →https://doi.org/10.1038/nprot.2016.136openalex-snapshot
The MaxQuant computational platform for mass spectrometry-based shotgun proteomics
inferredcites →https://doi.org/10.1038/srep46549openalex-snapshot
Detection of a new pyrethroid resistance mutation (V410L) in the sodium channel of Aedes aegypti: a potential challenge for mosquito control
inferredcites →https://doi.org/10.1042/bst0190755openalex-snapshot
Role of esterases in resistance of insects to insecticides
inferredcites →https://doi.org/10.1093/bioinformatics/btl328openalex-snapshot
Robust estimation of the false discovery rate
inferredcites →https://doi.org/10.1093/bioinformatics/btw580openalex-snapshot
DAPAR & ProStaR: software to perform statistical analyses in quantitative discovery proteomics
inferredcites →https://doi.org/10.1093/jee/100.2.545openalex-snapshot
Insecticide Susceptible/Resistance Status in Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus (Diptera: Culicidae) in Thailand During 2003-2005
inferredcites →https://doi.org/10.1093/nar/gkv007openalex-snapshot
limma powers differential expression analyses for RNA-sequencing and microarray studies
inferredcites →https://doi.org/10.1093/nar/gkv1145openalex-snapshot
2016 update of the PRIDE database and its related tools
inferredcites →https://doi.org/10.1093/nar/gkw419openalex-snapshot
Heatmapper: web-enabled heat mapping for all
inferredcites →https://doi.org/10.1093/nar/gkw880openalex-snapshot
2016 update of the PRIDE database and its related tools
inferredcites →https://doi.org/10.1093/toxsci/kft066openalex-snapshot
Aldehyde Oxidase Importance In Vivo in Xenobiotic Metabolism: Imidacloprid Nitroreduction in Mice
inferredcites →https://doi.org/10.1098/rstb.2012.0429openalex-snapshot
Role of cytochrome P450s in insecticide resistance: impact on the control of mosquito-borne diseases and use of insecticides on Earth
inferredcites →https://doi.org/10.1101/gr.189225.115openalex-snapshot
Identifying genomic changes associated with insecticide resistance in the dengue mosquito Aedes aegypti by deep targeted sequencing
inferredcites →https://doi.org/10.1111/eva.12867openalex-snapshot
Combining genetic crosses and pool targeted DNA‐seq for untangling genomic variations associated with resistance to multiple insecticides in the mosquito Aedes aegypti
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00774.xopenalex-snapshot
A mutation in the voltage‐gated sodium channel gene associated with pyrethroid resistance in Latin American Aedes aegypti
inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00967.xopenalex-snapshot
Transcription profiling of eleven cytochrome P450s potentially involved in xenobiotic metabolism in the mosquito Aedes aegypti
inferredcites →https://doi.org/10.1111/j.1365-3156.2010.02489.xopenalex-snapshot
Effectiveness of peridomestic space spraying with insecticide on dengue transmission; systematic review
inferredcites →https://doi.org/10.1111/j.1365-3156.2011.02725.xopenalex-snapshot
High‐throughput assays for detection of the F1534C mutation in the voltage‐gated sodium channel gene in permethrin‐resistant Aedes aegypti and the distribution of this mutation throughout Thailand
inferredcites →https://doi.org/10.1111/mve.12241openalex-snapshot
Insecticide resistance, associated mechanisms and fitness aspects in two B razilian S tegomyia aegypti (= A edes aegypti ) populations
inferredcites →https://doi.org/10.1146/annurev.ento.45.1.371openalex-snapshot
Insecticide Resistance in Insect Vectors of Human Disease
inferredcites →https://doi.org/10.1186/1471-2164-10-494openalex-snapshot
Exploring the molecular basis of insecticide resistance in the dengue vector Aedes aegypti: a case study in Martinique Island (French West Indies)
inferredcites →https://doi.org/10.1186/1471-2164-9-538openalex-snapshot
Expression of the cytochrome P450s, CYP6P3 and CYP6M2 are significantly elevated in multiple pyrethroid resistant populations of Anopheles gambiae s.s. from Southern Benin and Nigeria
inferredcites →https://doi.org/10.1186/1756-3305-4-5openalex-snapshot
Insecticide resistance in Aedes aegypti populations from Ceará, Brazil
inferredcites →https://doi.org/10.1186/1756-3305-7-25openalex-snapshot
Distribution and dissemination of the Val1016Ile and Phe1534Cys Kdr mutations in Aedes aegypti Brazilian natural populations
inferredcites →https://doi.org/10.1186/1756-3305-7-450openalex-snapshot
Mutations in the voltage-gated sodium channel gene of anophelines and their association with resistance to pyrethroids – a review
inferredcites →https://doi.org/10.1186/s13071-015-0797-2openalex-snapshot
Contrasting patterns of insecticide resistance and knockdown resistance (kdr) in the dengue vectors Aedes aegypti and Aedes albopictus from Malaysia
inferredcites →https://doi.org/10.1186/s13071-015-0833-2openalex-snapshot
Malaria vectors resistance to insecticides in Benin: current trends and mechanisms involved
inferredcites →https://doi.org/10.1186/s13071-015-0933-zopenalex-snapshot
Relationship between insecticide resistance and kdr mutations in the dengue vector Aedes aegypti in Southern China
inferredcites →https://doi.org/10.1186/s13071-016-1713-0openalex-snapshot
Additive effect of knockdown resistance mutations, S989P, V1016G and F1534C, in a heterozygous genotype conferring pyrethroid resistance in Aedes aegypti in Thailand
inferredcites →https://doi.org/10.1186/s13071-017-2215-4openalex-snapshot
Knockdown resistance (kdr) of the voltage-gated sodium channel gene of Aedes aegypti population in Denpasar, Bali, Indonesia
inferredcites →https://doi.org/10.1186/s13071-017-2581-yopenalex-snapshot
Evidence for multiple-insecticide resistance in urban Aedes albopictus populations in southern China
inferredcites →https://doi.org/10.1186/s13071-019-3309-yopenalex-snapshot
Presence of the point mutations Val1016Gly in the voltage-gated sodium channel detected in a single mosquito from Panama
inferredcites →https://doi.org/10.1186/s13071-019-3739-6openalex-snapshot
Susceptibility to insecticides and resistance mechanisms in three populations of Aedes aegypti from Peru
inferredcites →https://doi.org/10.1186/s40249-017-0254-xopenalex-snapshot
Levels of insecticide resistance to deltamethrin, malathion, and temephos, and associated mechanisms in Aedes aegypti mosquitoes from the Guadeloupe and Saint Martin islands (French West Indies)
inferredcites →https://doi.org/10.1303/aez.2010.275openalex-snapshot
Point mutations in domain II of the voltage-gated sodium channel gene in deltamethrin-resistant Aedes aegypti (Diptera: Culicidae)
inferredcites →https://doi.org/10.1371/journal.pgen.1004236openalex-snapshot
CYP6 P450 Enzymes and ACE-1 Duplication Produce Extreme and Multiple Insecticide Resistance in the Malaria Mosquito Anopheles gambiae
inferredcites →https://doi.org/10.1371/journal.pntd.0002743openalex-snapshot
Identification of Carboxylesterase Genes Implicated in Temephos Resistance in the Dengue Vector Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pntd.0002948openalex-snapshot
Mechanisms of Pyrethroid Resistance in the Dengue Mosquito Vector, Aedes aegypti: Target Site Insensitivity, Penetration, and Metabolism
inferredcites →https://doi.org/10.1371/journal.pntd.0004226openalex-snapshot
Deltamethrin Resistance Mechanisms in Aedes aegypti Populations from Three French Overseas Territories Worldwide
inferredcites →https://doi.org/10.1371/journal.pntd.0005526openalex-snapshot
In the hunt for genomic markers of metabolic resistance to pyrethroids in the mosquito Aedes aegypti: An integrated next-generation sequencing approach
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.pntd.0005799openalex-snapshot
Insecticide resistance is mediated by multiple mechanisms in recently introduced Aedes aegypti from Madeira Island (Portugal)
inferredcites →https://doi.org/10.1371/journal.pntd.0006390openalex-snapshot
Pyrethroid resistance persists after ten years without usage against Aedes aegypti in governmental campaigns: Lessons from São Paulo State, Brazil
inferredcites →https://doi.org/10.1371/journal.pntd.0007615openalex-snapshot
Management of insecticide resistance in the major Aedes vectors of arboviruses: Advances and challenges
inferredcites →https://doi.org/10.1371/journal.pone.0030989openalex-snapshot
Insecticide Resistance in the Dengue Vector Aedes aegypti from Martinique: Distribution, Mechanisms and Relations with Environmental Factors
inferredcites →https://doi.org/10.1590/0074-02760170398openalex-snapshot
Successes and failures of sixty years of vector control in French Guiana: what is the next step?
inferredcites →https://doi.org/10.1590/s0074-02762011000300015openalex-snapshot
Multiple insecticide resistance in Aedes aegypti (Diptera: Culicidae) populations compromises the effectiveness of dengue vector control in French Guiana
inferredcites →https://doi.org/10.1603/0022-2585-39.6.882openalex-snapshot
Cross-Resistance to Pyrethroid and Organophosphorus Insecticides Induced by Selection with Temephos inAedes aegypti(Diptera: Culicidae) from Cuba
inferredcites →https://doi.org/10.1603/ec12284openalex-snapshot
Wide Spread Cross Resistance to Pyrethroids in Aedes aegypti (Diptera: Culicidae) From Veracruz State Mexico
inferredcites →https://doi.org/10.2174/138920006774832596openalex-snapshot
Inhibition of Sulfotransferases by Xenobiotics
inferredcites →https://doi.org/10.2987/11-6203.1openalex-snapshot
Discriminating Lethal Concentrations and Efficacy of Six Pyrethroids for Control of Aedes aegypti in Thailand
inferredcites →https://doi.org/10.2987/8756-971x(2006)22[672:moirif]2.0.co;2openalex-snapshot
MECHANISMS OF INSECTICIDE RESISTANCE IN FIELD POPULATIONS OF AEDES AEGYPTI (L.) FROM QUINTANA ROO, SOUTHERN MEXICO
inferredcites →https://doi.org/10.3201/eid0404.980410openalex-snapshot
Insecticide Resistance and Vector Control
inferredcites →https://doi.org/10.32614/cran.package.imp4popenalex-snapshot
imp4p: Imputation for Proteomics
inferredcites →https://doi.org/10.3390/ijms20112829openalex-snapshot
Insect ATP-Binding Cassette (ABC) Transporters: Roles in Xenobiotic Detoxification and Bt Insecticidal Activity
inferredcites →https://doi.org/10.3390/insects7040060openalex-snapshot
Sodium Channel Mutations and Pyrethroid Resistance in Aedes aegypti
inferredcites →https://doi.org/10.4269/ajtmh.1987.37.37openalex-snapshot
A Ribosomal RNA Gene Probe Differentiates Member Species of the Anopheles gambiae Complex
inferredcites →https://doi.org/10.5897/jpvb.9000020openalex-snapshot
Response of Culex quinquefasciatus to deltamethrin in Lahore district
inferredcites →https://doi.org/10.7554/elife.08347openalex-snapshot
The global distribution of the arbovirus vectors Aedes aegypti and Ae. albopictus

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1590/1806-9665-rbent-2025-0072zenodo-depositor-declared
Current susceptibility status and resistance mechanisms to pyrethroids and organophosphates in Aedes aegypti (Diptera, Culicidae) from Atlantico, Colombia
inferred← citeshttps://doi.org/10.1007/s10340-024-01747-4openalex-snapshot
Efficacy and selectivity of Sextonia rubra wood extracts and formulation in the control of Aedes aegypti strains
inferred← citeshttps://doi.org/10.1016/j.toxrep.2021.11.013openalex-snapshot
Gradual reduction of susceptibility and enhanced detoxifying enzyme activities of laboratory-reared Aedes aegypti under exposure of temephos for 28 generations
inferred← citeshttps://doi.org/10.1016/j.xgen.2025.100924openalex-snapshot
Single-cell transcriptional landscapes of Aedes aegypti midgut and fat body after a bloodmeal
inferred← citeshttps://doi.org/10.1038/s41598-023-43676-9openalex-snapshot
Time-series analysis of transcriptomic changes due to permethrin exposure reveals that Aedes aegypti undergoes detoxification metabolism over 24 h
inferred← citeshttps://doi.org/10.1093/etojnl/vgaf040openalex-snapshot
Application of omics technology in ecotoxicology of arthropod in farmland
inferred← citeshttps://doi.org/10.1093/jme/tjac138openalex-snapshot
First Report of Mutations Associated With Pyrethroid (L1014F) and Organophosphate (G119S) Resistance in Belgian Culex (Diptera: Culicidae) Mosquitoes
inferred← citeshttps://doi.org/10.1101/2023.03.13.532092openalex-snapshot
Molecular signature of domestication in the arboviral vector Aedes aegypti
inferred← citeshttps://doi.org/10.1101/2024.11.08.622039openalex-snapshot
Single-cell transcriptional landscapes of Aedes aegypti midgut and fat body after a bloodmeal
inferred← citeshttps://doi.org/10.1111/mve.12593openalex-snapshot
Interactions between vector competence to chikungunya virus and resistance to deltamethrin in Aedes aegypti laboratory lines?
inferred← citeshttps://doi.org/10.1186/s13071-021-05146-xopenalex-snapshot
BioRssay: an R package for analyses of bioassays and probit graphs
inferred← citeshttps://doi.org/10.1186/s13071-023-05696-2openalex-snapshot
Enrichment of phenotype among biological forms of Anopheles stephensi Liston through establishment of isofemale lines
inferred← citeshttps://doi.org/10.1186/s13071-025-06675-5openalex-snapshot
Characterization of the transcriptional cellular response in midgut tissue of temephos-resistant Aedes aegypti larvae
inferred← citeshttps://doi.org/10.1210/jendso/bvac145openalex-snapshot
Deletion of Constitutive Androstane Receptor Led to Intestinal Alterations and Increased Imidacloprid in Murine Liver
inferred← citeshttps://doi.org/10.1371/journal.pntd.0011604openalex-snapshot
Quantitative proteomics analysis of permethrin and temephos-resistant Ae. aegypti revealed diverse differentially expressed proteins associated with insecticide resistance from Penang Island, Malaysia
inferred← citeshttps://doi.org/10.1371/journal.pone.0293124openalex-snapshot
Larvicidal properties of terpenoid-based nanoemulsions against the dengue vector Aedes aegypti L. and their potential toxicity against non-target organism
inferred← citeshttps://doi.org/10.1371/journal.pone.0303027openalex-snapshot
Potential of MALDI-TOF MS biotyping to detect deltamethrin resistance in the dengue vector Aedes aegypti
inferred← citeshttps://doi.org/10.1371/journal.pone.0309201openalex-snapshot
Assessing pyrethroid resistance in Aedes aegypti from Cordoba Colombia: Implications of kdr mutations
inferred← citeshttps://doi.org/10.21149/13910openalex-snapshot
Current enzyme-mediated insecticide resistance status of Aedes aegypti populations from a dengue-endemic city in southern Mexico
inferred← citeshttps://doi.org/10.24072/pcjournal.497openalex-snapshot
A genomic duplication spanning multiple P450s contributes to insecticide resistance in the dengue mosquito Aedes aegypti
inferred← citeshttps://doi.org/10.3390/genes14081626openalex-snapshot
Comparative Transcriptomic Analysis of Insecticide-Resistant Aedes aegypti from Puerto Rico Reveals Insecticide-Specific Patterns of Gene Expression
inferred← citeshttps://doi.org/10.3390/insects12080752openalex-snapshot
Evaluation of Total Female and Male Aedes aegypti Proteomes Reveals Significant Predictive Protein–Protein Interactions, Functional Ontologies, and Differentially Abundant Proteins
inferred← citeshttps://doi.org/10.3390/insects14100797openalex-snapshot
Viral Prevalence and Genomic Xenology in the Coevolution of HzNV-2 (Nudiviridae) with Host Helicoverpa zea (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.3390/insects16020106openalex-snapshot
Long-Term Exposure to Lambda-Cyhalothrin Reveals Novel Genes Potentially Involved in Aedes aegypti Insecticide Resistance
inferred← citeshttps://doi.org/10.3390/proteomes10040038openalex-snapshot
Impact of CHIKV Replication on the Global Proteome of Aedes albopictus Cells
inferred← citeshttps://doi.org/10.3390/tropicalmed10060171openalex-snapshot
Deltamethrin Selection Drives Transcriptomic Changes in Detoxification, Immune, and Cuticle Genes in Aedes aegypti
inferred← citeshttps://doi.org/10.55446/ije.2025.2979openalex-snapshot
Detoxification Enzymes in the Carmine Spider Mite Tetranychus cinnabarinus Boisduval
inferred← citeshttps://doi.org/10.55446/ije.2025.3137openalex-snapshot
Resistance Mechanisms in Aedes spp. and Dengue Vector Control in Indonesia - A Review
inferred← citeshttps://doi.org/10.70675/7d6a2145z05d7z4746zb3ffza3e40f94dc6bopenalex-snapshot
MALDI-TOF MS profiling for multiple life traits in Mosquitoes of Public Health Importance
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