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Detection of a new pyrethroid resistance mutation (V410L) in the sodium channel of Aedes aegypti: a potential challenge for mosquito control

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.1909.02550020033007openalex-snapshot

A JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

inferredcites →https://doi.org/10.1007/s00204-011-0726-xopenalex-snapshot

Molecular mechanisms of pyrethroid insecticide neurotoxicity: recent advances

inferredcites →https://doi.org/10.1016/0092-8674(95)90279-1openalex-snapshot

Cloning and functional analysis of tipE, a novel membrane protein that enhances drosophila para sodium channel function

inferredcites →https://doi.org/10.1016/b0-44-451924-6/00049-1openalex-snapshot

Insect Cytochrome P450

inferredcites →https://doi.org/10.1016/b0-44-451924-6/00074-0openalex-snapshot

Glutathione Transferases

inferredcites →https://doi.org/10.1016/b978-0-12-417010-0.00005-7openalex-snapshot

Voltage-Gated Sodium Channels as Insecticide Targets

inferredcites →https://doi.org/10.1016/c2021-1-02770-5openalex-snapshot

Comprehensive Molecular Insect Science

inferredcites →https://doi.org/10.1016/j.actatropica.2016.02.021openalex-snapshot

Deltamethrin-mediated survival, behavior, and oenocyte morphology of insecticide-susceptible and resistant yellow fever mosquitos (Aedes aegypti)

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.2010.09.005openalex-snapshot

A sodium channel mutation identified in Aedes aegypti selectively reduces cockroach sodium channel sensitivity to type I, but not type II pyrethroids

inferredcites →https://doi.org/10.1016/j.ibmb.2014.03.012openalex-snapshot

Molecular biology of insect sodium channels and pyrethroid resistance

inferredcites →https://doi.org/10.1016/j.neuro.2013.06.001openalex-snapshot

A residue in the transmembrane segment 6 of domain I in insect and mammalian sodium channels regulate differential sensitivities to pyrethroid insecticides

inferredcites →https://doi.org/10.1016/j.neuro.2016.08.013openalex-snapshot

Elucidation of pyrethroid and DDT receptor sites in the voltage-gated sodium channel

inferredcites →https://doi.org/10.1016/j.pestbp.2009.06.010openalex-snapshot

State-dependent modification of voltage-gated sodium channels by pyrethroids

inferredcites →https://doi.org/10.1016/j.pestbp.2013.02.007openalex-snapshot

Diversity and convergence of sodium channel mutations involved in resistance to pyrethroids

inferredcites →https://doi.org/10.1016/j.pestbp.2016.03.005openalex-snapshot

Pyrethroid resistance in Aedes aegypti and Aedes albopictus: Important mosquito vectors of human diseases

inferredcites →https://doi.org/10.1016/j.pt.2015.11.010openalex-snapshot

Insecticide Resistance in African Anopheles Mosquitoes: A Worsening Situation that Needs Urgent Action to Maintain Malaria Control

inferredcites →https://doi.org/10.1016/j.taap.2010.05.016openalex-snapshot

A negative charge in transmembrane segment 1 of domain II of the cockroach sodium channel is critical for channel gating and action of pyrethroid insecticides

inferredcites →https://doi.org/10.1016/s0022-3565(25)22418-1openalex-snapshot

Differential mechanism of action of the pyrethroid tetramethrin on tetrodotoxin-sensitive and tetrodotoxin-resistant sodium channels.

inferredcites →https://doi.org/10.1016/s0965-1748(99)00038-7openalex-snapshot

Cytochromes P450 and insecticide resistance

inferredcites →https://doi.org/10.1021/bk-1990-0421.ch002openalex-snapshot

Overview of Insecticide Resistance

inferredcites →https://doi.org/10.1042/bj20051925openalex-snapshot

Modelling insecticide-binding sites in the voltage-gated sodium channel

inferredcites →https://doi.org/10.1073/pnas.0901369106openalex-snapshot

Using adult mosquitoes to transfer insecticides to Aedes aegypti larval habitats

inferredcites →https://doi.org/10.1073/pnas.1201475109openalex-snapshot

Footprints of positive selection associated with a mutation ( N1575Y ) in the voltage-gated sodium channel of Anopheles gambiae

inferredcites →https://doi.org/10.1073/pnas.1305118110openalex-snapshot

Molecular evidence for dual pyrethroid-receptor sites on a mosquito sodium channel

inferredcites →https://doi.org/10.1085/jgp.110.2.119openalex-snapshot

Functional Expression ofDrosophila paraSodium Channels

inferredcites →https://doi.org/10.1085/jgp.115.3.305openalex-snapshot

Activation ofDrosophilaSodium Channels Promotes Modification by Deltamethrin

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/10.1124/mol.104.006205openalex-snapshot

Identification of Amino Acid Residues in the Insect Sodium Channel Critical for Pyrethroid Binding

inferredcites →https://doi.org/10.1124/mol.115.098707openalex-snapshot

Rotational Symmetry of Two Pyrethroid Receptor Sites in the Mosquito Sodium Channel

inferredcites →https://doi.org/10.1126/science.1078052openalex-snapshot

An Overview of Insecticide Resistance

inferredcites →https://doi.org/10.1146/annurev-ento-010814-020828openalex-snapshot

Insecticide Resistance in Mosquitoes: Impact, Mechanisms, and Research Directions

inferredcites →https://doi.org/10.1155/2016/8603263openalex-snapshot

Resistance Status to the Insecticides Temephos, Deltamethrin, and Diflubenzuron in BrazilianAedes aegyptiPopulations

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/10.1201/9781315373775openalex-snapshot

Bioassays with Arthropods

inferredcites →https://doi.org/10.1371/journal.pntd.0003085openalex-snapshot

A Single Crossing-Over Event in Voltage-Sensitive Na+ Channel Genes May Cause Critical Failure of Dengue Mosquito Control by Insecticides

inferredcites →https://doi.org/10.1371/journal.pntd.0004769openalex-snapshot

Control of Urban Zika Vectors: Should We Return to the Successful PAHO/WHO Strategy?

inferredcites →https://doi.org/10.1371/journal.pone.0023403openalex-snapshot

Multiple Cytochrome P450 Genes: Their Constitutive Overexpression and Permethrin Induction in Insecticide Resistant Mosquitoes, Culex quinquefasciatus

inferredcites →https://doi.org/10.1371/journal.pone.0060878openalex-snapshot

Assessing the Effects of Aedes aegypti kdr Mutations on Pyrethroid Resistance and Its Fitness Cost

inferredcites →https://doi.org/10.1590/0037-8682-0046-2015openalex-snapshot

Phenotypic and genotypic profile of pyrethroid resistance in populations of the mosquito Aedes aegypti from Goiânia, Central West Brazil

inferredcites →https://doi.org/10.1590/0074-02760150409openalex-snapshot

Spatial and temporal country-wide survey of temephos resistance in Brazilian populations of Aedes aegypti

What points at this work

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

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Current susceptibility status and resistance mechanisms to pyrethroids and organophosphates in Aedes aegypti (Diptera, Culicidae) from Atlantico, Colombia

inferred← citeshttps://doi.org/10.1002/arch.21686openalex-snapshot

Chronology of sodium channel mutations associated with pyrethroid resistance in Aedes aegypti

inferred← citeshttps://doi.org/10.1002/ps.4801openalex-snapshot

Alternative control of Aedes aegypti resistant to pyrethroids: lethal and sublethal effects of monoterpene bioinsecticides

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1002/ps.5763openalex-snapshot

The F1534C voltage‐sensitive sodium channel mutation confers 7‐ to 16‐fold resistance to pyrethroid insecticides in Aedes aegypti

inferred← citeshttps://doi.org/10.1002/ps.6324openalex-snapshot

A first, naturally occurring substitution at the second pyrethroid receptor of voltage‐gated sodium channel of Aedes aegypti

inferred← citeshttps://doi.org/10.1002/ps.6597openalex-snapshot

Effects of piperonyl butoxide synergism and cuticular thickening on the contact irritancy response of field Aedes aegypti (Diptera: Culicidae) to deltamethrin

inferred← citeshttps://doi.org/10.1002/ps.6602openalex-snapshot

Impact of selection regime and introgression on deltamethrin resistance in the arbovirus vector Aedes aegypti – a comparative study between contrasted situations in New Caledonia and French Guiana

inferred← citeshttps://doi.org/10.1002/ps.6682openalex-snapshot

Bioallethrin activates specific olfactory sensory neurons and elicits spatial repellency in Aedes aegypti

inferred← citeshttps://doi.org/10.1002/ps.6731openalex-snapshot

In vivo functional validation of the V402L voltage gated sodium channel mutation in the malaria vector An. gambiae

inferred← citeshttps://doi.org/10.1002/ps.7999openalex-snapshot

Insecticide resistance status of Aedes aegypti in border areas of Yunnan Province

inferred← citeshttps://doi.org/10.1002/ps.8495openalex-snapshot

The V410L kdr allele in the VGSC confers higher levels of field resistance to permethrin in urban mosquito populations of Aedes aegypti (L.)

inferred← citeshttps://doi.org/10.1002/ps.8625openalex-snapshot

Alanine to glycine substitution in the PyR2 confers sodium channel resistance to Type I pyrethroids

inferred← citeshttps://doi.org/10.1007/978-981-97-4163-2_15openalex-snapshot

Insecticidal Resistance and Counter Mechanism in Mosquitoes: A Coevolutionary Trade-off

inferred← citeshttps://doi.org/10.1007/s10164-020-00651-5openalex-snapshot

Behavioural changes in Tityus stigmurus (Thorell, 1876) (SCORPIONES: BUTHIDAE) exposed to a pyrethroid insecticide

inferred← citeshttps://doi.org/10.1007/s10340-021-01389-wopenalex-snapshot

A potential lignan botanical insecticide from Phryma leptostachya against Aedes aegypti: laboratory selection, metabolic mechanism, and resistance risk assessment

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Bti-based insecticide enhances the predatory abilities of the backswimmer Buenoa tarsalis (Hemiptera: Notonectidae)

inferred← citeshttps://doi.org/10.1007/s10646-022-02562-2openalex-snapshot

Sublethal exposure to pyriproxyfen does not impair the abilities of the backswimmer Buenoa amnigenus to prey upon Aedes aegypti larvae

inferred← citeshttps://doi.org/10.1007/s11033-026-12410-9openalex-snapshot

Insecticide resistance in mosquitoes: Current status, mechanism, monitoring and innovative strategies for sustainable vector control

inferred← citeshttps://doi.org/10.1007/s11356-024-33440-5openalex-snapshot

Essential oil and fenchone extracted from Tetradenia riparia (Hochstetter.) Codd (Lamiaceae) induce oxidative stress in Culex quinquefasciatus larvae (Diptera: Culicidae) without causing lethal effects on non-target animals

inferred← citeshttps://doi.org/10.1007/s13205-021-02716-9openalex-snapshot

Rhamnolipids on Aedes aegypti larvae: a potential weapon against resistance selection

inferred← citeshttps://doi.org/10.1007/s13744-019-00710-8openalex-snapshot

Life History Traits and Predatory Performance of Belostoma anurum (Hemiptera: Belostomatidae), a Biological Control Agent of Disease Vector Mosquitoes

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Nanoemulsion Loaded with Volatile Oil from Piper alatipetiolatum as an Alternative Agent in the Control of Aedes aegypti

inferred← citeshttps://doi.org/10.1016/bs.aiip.2026.05.002openalex-snapshot

Insecticide resistance in mosquitoes: Molecular mechanisms and evolutionary dynamics

inferred← citeshttps://doi.org/10.1016/j.actatropica.2017.12.024openalex-snapshot

Mating behavior of the West Nile virus vector Culex pipiens – role of behavioral asymmetries

inferred← citeshttps://doi.org/10.1016/j.actatropica.2023.106919openalex-snapshot

Insecticide susceptibility and detection of kdr-gene mutations in Aedes aegypti of Peshawar, Pakistan

inferred← citeshttps://doi.org/10.1016/j.actatropica.2023.106937openalex-snapshot

Co-occurrence of multiple kdr mutations (F1534C, V1016I, V410L) in Aedes aegypti from coastal areas in Ghana and assessment of the role of mosquito coil in causing pyrethroid resistance

inferred← citeshttps://doi.org/10.1016/j.actatropica.2025.107736openalex-snapshot

Insecticide susceptibility and knockdown resistance mutations in Aedes aegypti and Culex species in Bangladesh

inferred← citeshttps://doi.org/10.1016/j.actatropica.2025.107847openalex-snapshot

Spatial distribution of insecticide resistance in Aedes aegypti (Diptera: Culicidae) across Burkina Faso highlights strengthened resistance management strategies

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In silico and in vivo study of adulticidal activity from Ayapana triplinervis essential oils nano-emulsion against Aedes aegypti

inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111719openalex-snapshot

Larvicidal mechanism of the rare sesquiterpene ishwarol B from Piper alatipetiolatum (Piperaceae) against Aedes aegypti, Anopheles darlingi, and Culex quinquefasciatus (Culicidae): oxidative damage, defense enzyme modulation, and acetylcholinesterase inhibition

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.10.061openalex-snapshot

Sublethal exposure to deltamethrin reduces the abilities of giant water bugs to prey upon Aedes aegypti larvae

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.01.068openalex-snapshot

Aedes aegypti larvae treated with spinosad produce adults with damaged midgut and reduced fecundity

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.142240openalex-snapshot

Exposure to low-concentration fipronil impairs survival, behavior, midgut morphology and physiology of Aedes aegypti larvae

inferred← citeshttps://doi.org/10.1016/j.cois.2024.101178openalex-snapshot

Recent advances in the study of knockdown resistance mutations in Aedes mosquitoes with a focus on several remarkable mutations

inferred← citeshttps://doi.org/10.1016/j.envpol.2020.116307openalex-snapshot

Biological, histological and immunohistochemical studies on the toxicity of spent coffee grounds and caffeine on the larvae of Aedes aegypti (Diptera: Culicidae)

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Detrimental effects of pyriproxyfen on the detoxification and abilities of Belostoma anurum to prey upon Aedes aegypti larvae

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A Unique Mechanism of Transfluthrin Action Revealed by Mapping its Binding Sites in the Mosquito Sodium Channel

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Amino acid and acylcarnitine profile of Aedes aegypti (L) post-blood feeding, after permethrin exposure, and during the life cycle

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Larvicidal effect of essential oils from Brazilian cultivars of guava on Aedes aegypti L.

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Mosquiticidal and repellent potential of formulations containing wood residue extracts of a Neotropical plant, Tabebuia heptaphylla

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Secondary metabolites produced by solid-state fermentation of a neotropical Aspergillus flavus strain confer anti-mosquito activity with long shelf-life

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Control failure and insecticides resistance in populations of Rhyzopertha dominica (Coleoptera: Bostrichidae) from Colombia

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Does use of domestic insecticides undermine public health control strategies?

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“Armed to the teeth”: The multiple ways to survive insecticidal and predatory challenges in Aedes aegypti larvae

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Efficacy of five commercial household insecticide aerosol sprays against pyrethroid resistant Aedes aegypti and Culex quinquefasciatus mosquitoes in Thailand

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Sodium channel-directed alkaloids synergize the mosquitocidal and neurophysiological effects of natural pyrethrins

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Rapid detection of kdr mutation F1534C in Aedes aegypti using recombinase polymerase amplification and lateral flow dipsticks

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Toxicity of the essential oil from Tetradenia riparia (Hochstetter.) Codd (Lamiaceae) and its principal constituent against malaria and dengue vectors and non-target animals

inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105490openalex-snapshot

Leucine to tryptophane substitution in the pore helix IIP1 confer sodium channel resistance to pyrethroids and DDT

inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105710openalex-snapshot

Correlation between pyrethroid knockdown resistance and mutation frequency of voltage-gated sodium channel and its application in Aedes aegypti management

inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106825openalex-snapshot

Arginine kinase 2 knockdown enhances deltamethrin sensitivity in Aedes aegypti

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Nationwide integrative analysis of pyrethroid resistance in Aedes aegypti from Mexico

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Target-site resistance genotype impacts temperature-dependent pyrethroid toxicity in Aedes aegypti

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Comparative study of three herbal formulations against dengue vectors Aedes aegypti

inferred← citeshttps://doi.org/10.1017/s0007485319000439openalex-snapshot

Occurrence of pyrethroid resistance mutation in Cydia pomonella (Lepidoptera: Tortricidae) throughout Argentina

inferred← citeshttps://doi.org/10.1038/s41598-018-25222-0openalex-snapshot

Parallel evolution of vgsc mutations at domains IS6, IIS6 and IIIS6 in pyrethroid resistant Aedes aegypti from Mexico

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Kdr genotyping in Aedes aegypti from Brazil on a nation-wide scale from 2017 to 2018

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Insecticide resistance and underlying targets-site and metabolic mechanisms in Aedes aegypti and Aedes albopictus from Lahore, Pakistan

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Repellency and insecticidal activity of seven Mugwort (Artemisia argyi) essential oils against the malaria vector Anopheles sinensis

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Genetic structure and kdr mutations in Aedes aegypti populations along a road crossing the Amazon Forest in Amapá State, Brazil

inferred← citeshttps://doi.org/10.1038/s41598-023-44457-0openalex-snapshot

Detection of insecticide resistance markers in Anopheles funestus from the Democratic Republic of the Congo using a targeted amplicon sequencing panel

inferred← citeshttps://doi.org/10.1038/s41598-025-03709-xopenalex-snapshot

Profiling insecticide resistance phenotypes and genotypes in Aedes aegypti populations across four regions in Puerto Rico

inferred← citeshttps://doi.org/10.1038/s41598-025-94738-zopenalex-snapshot

Impact of Aedes aegypti V1016I and F1534C knockdown resistance genotypes on operational interventions

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Select Plant Essential Oils Enhance the Toxicity of Permethrin Against a Pyrethroid-susceptible and Pyrethroid-resistant Strain of Aedes aegypti

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Lack of fitness cost in field-collected populations of Musca domestica with different susceptibilities to pyrethroids, neonicotinoids, and their combination

inferred← citeshttps://doi.org/10.1080/21505594.2026.2723655openalex-snapshot

Advances in mosquito gut microbiota: Mechanisms of regulating pathogen transmission and applications in vector control

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Toxicity of Silybum marianum and Nerium oleander extracts against Mosquito Larvae of Culex quinquefasciatus (Say)

inferred← citeshttps://doi.org/10.1093/gbe/evaf066openalex-snapshot

Demographic History, Genetic Load, and the Efficacy of Selection in the Globally Invasive Mosquito Aedes aegypti

inferred← citeshttps://doi.org/10.1093/jisesa/ieaa060openalex-snapshot

Low Levels of Pyrethroid Resistance in Hybrid Offspring of a Highly Resistant and a More Susceptible Mosquito Strain

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Screening Aedes aegypti (Diptera: Culicidae) Populations From Pernambuco, Brazil for Resistance to Temephos, Diflubenzuron, and Cypermethrin and Characterization of Potential Resistance Mechanisms

inferred← citeshttps://doi.org/10.1093/jme/tjab045openalex-snapshot

Insecticide Resistance Patterns and Mechanisms in Aedes aegypti (Diptera: Culicidae) Populations Across Abidjan, Côte d’Ivoire Reveal Emergent Pyrethroid Resistance

inferred← citeshttps://doi.org/10.1093/jme/tjac120openalex-snapshot

Evidence of High Frequencies of Insecticide Resistance Mutations in Aedes aegypti (Culicidae) Mosquitoes in Urban Accra, Ghana: Implications for Insecticide-based Vector Control of Aedes-borne Arboviral Diseases

inferred← citeshttps://doi.org/10.1093/jme/tjad015openalex-snapshot

A Globally Distributed Insecticide Resistance Allele Confers a Fitness Cost in the Absence of Insecticide in Aedes aegypti (Diptera: Culicidae), the Yellow Fever Mosquito

inferred← citeshttps://doi.org/10.1093/jme/tjy016openalex-snapshot

Mosquitocidal Activity of a Naturally Occurring Isochroman and Synthetic Analogs from the Plant Pathogenic Fungus, Diaporthe eres Against Aedes aegypti (Diptera: Culicidae)

inferred← citeshttps://doi.org/10.1093/jme/tjz148openalex-snapshot

Distribution and Frequency of the kdr Mutation V410L in Natural Populations of Aedes aegypti (L.) (Diptera: Culicidae) From Eastern and Southern Mexico

inferred← citeshttps://doi.org/10.1093/jme/tjz241openalex-snapshot

Co-occurrence of kdr Mutations V1016I and F1534C and Its Association With Phenotypic Resistance to Pyrethroids in Aedes aegypti (Diptera: Culicidae) Populations From Costa Rica

inferred← citeshttps://doi.org/10.1093/molbev/msad072openalex-snapshot

Strong Positive Selection in Aedes aegypti and the Rapid Evolution of Insecticide Resistance

inferred← citeshttps://doi.org/10.1093/procel/pwad021openalex-snapshot

Impact of the microbiome on mosquito-borne diseases

inferred← citeshttps://doi.org/10.1101/2020.02.25.964270openalex-snapshot

The need to harmonize insecticide resistance testing: methodology, intensity concentrations and molecular mechanisms evaluated in Aedes aegypti populations in Central America and Hispaniola

inferred← citeshttps://doi.org/10.1101/2021.11.08.467678openalex-snapshot

Insecticide susceptibility of Aedes (Stegomyia) aegypti (Linnaeus, 1762) and Aedes (Stegomyia) albopictus (Skuse, 1894) in Kinshasa, Democratic Republic of the Congo

inferred← citeshttps://doi.org/10.1101/2023.05.11.540334openalex-snapshot

Pyrethroid susceptibility reversal in Aedes aegypti: a longitudinal study in Tapachula, Mexico

inferred← citeshttps://doi.org/10.1101/2024.03.07.584008openalex-snapshot

Demographic history and the efficacy of selection in the globally invasive mosquito Aedes aegypti

inferred← citeshttps://doi.org/10.1101/2025.10.31.685655openalex-snapshot

The contribution of transposable element insertions to genetic diversity in Aedes aegypti populations

inferred← citeshttps://doi.org/10.1101/740829openalex-snapshot

A new knockdown resistance ( kdr ) mutation, F1534L, in the voltage-gated sodium channel of Aedes aegypti , co-occurring with F1534C, S989P and V1016G

inferred← citeshttps://doi.org/10.1111/1744-7917.12498openalex-snapshot

High throughput sequencing reveals Drosophila suzukii responses to insecticides

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1111/eva.13269openalex-snapshot

Rapid evolution of knockdown resistance haplotypes in response to pyrethroid selection in Aedes aegypti

inferred← citeshttps://doi.org/10.1111/eva.70305openalex-snapshot

The Evolution of Knockdown Resistance: Genotypic and Phenotypic Insights Into Aedes aegypti Insecticide Resistance

inferred← citeshttps://doi.org/10.1111/imb.12575openalex-snapshot

Exome‐wide association of deltamethrin resistance in Aedes aegypti from Mexico

inferred← citeshttps://doi.org/10.1111/imb.12605openalex-snapshot

Conservation of the voltage‐sensitive sodium channel protein within the Insecta

inferred← citeshttps://doi.org/10.1111/jvec.12298openalex-snapshot

Two novel mutations in the voltage-gated sodium channel associated with knockdown resistance (kdr) in the dengue vectorAedes aegyptiin Vietnam

inferred← citeshttps://doi.org/10.1111/mec.15430openalex-snapshot

Heterogeneous genetic invasions of three insecticide resistance mutations in Indo‐Pacific populations of Aedes aegypti (L.)

inferred← citeshttps://doi.org/10.1111/mve.12580openalex-snapshot

Detection of pyrethroid resistance mutations and intron variants in the voltage‐gated sodium channel of Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus mosquitoes from Lao People's Democratic Republic

inferred← citeshttps://doi.org/10.1111/mve.12602openalex-snapshot

Multiple insecticide resistance and first evidence of V410L kdr mutation in Aedes (Stegomyia) aegypti (Linnaeus) from Burkina Faso

inferred← citeshttps://doi.org/10.1126/sciadv.abq7345openalex-snapshot

Discovery of super–insecticide-resistant dengue mosquitoes in Asia: Threats of concomitant knockdown resistance mutations

inferred← citeshttps://doi.org/10.1127/entomologia/2023/1880openalex-snapshot

Pyrethroid resistance mechanisms in the major malaria vector species complex

inferred← citeshttps://doi.org/10.1146/annurev-ento-011118-112420openalex-snapshot

Life and Death at the Voltage-Sensitive Sodium Channel: Evolution in Response to Insecticide Use

inferred← citeshttps://doi.org/10.1186/s12985-026-03127-zopenalex-snapshot

Furin as target for suppression of mosquito-borne viruses

inferred← citeshttps://doi.org/10.1186/s13071-018-3113-0openalex-snapshot

First report of V1016G and S989P knockdown resistant (kdr) mutations in pyrethroid-resistant Sri Lankan Aedes aegypti mosquitoes

inferred← citeshttps://doi.org/10.1186/s13071-020-04093-3openalex-snapshot

Impact of deltamethrin selection on kdr mutations and insecticide detoxifying enzymes in Aedes aegypti from Mexico

inferred← citeshttps://doi.org/10.1186/s13071-020-04127-wopenalex-snapshot

Evaluation of resistance to pyrethroid and organophosphate adulticides and kdr genotyping in Aedes aegypti populations from Roraima, the northernmost Brazilian State

inferred← citeshttps://doi.org/10.1186/s13071-020-04201-3openalex-snapshot

A new knockdown resistance (kdr) mutation, F1534L, in the voltage-gated sodium channel of Aedes aegypti, co-occurring with F1534C, S989P and V1016G

inferred← citeshttps://doi.org/10.1186/s13071-020-04238-4openalex-snapshot

Identifying the fitness costs of a pyrethroid-resistant genotype in the major arboviral vector Aedes aegypti

inferred← citeshttps://doi.org/10.1186/s13071-020-04284-yopenalex-snapshot

Resistance to commonly used insecticides and underlying mechanisms of resistance in Aedes aegypti (L.) from Sri Lanka

inferred← citeshttps://doi.org/10.1186/s13071-020-04304-xopenalex-snapshot

Frequency of kdr mutations in the voltage-sensitive sodium channel (VSSC) gene in Aedes aegypti from Yogyakarta and implications for Wolbachia-infected mosquito trials

inferred← citeshttps://doi.org/10.1186/s13071-020-04356-zopenalex-snapshot

Surveillance of Aedes aegypti populations in the city of Praia, Cape Verde: Zika virus infection, insecticide resistance and genetic diversity

inferred← citeshttps://doi.org/10.1186/s13071-020-04503-6openalex-snapshot

Insecticide resistance status of Aedes aegypti in Bangladesh

inferred← citeshttps://doi.org/10.1186/s13071-021-04627-3openalex-snapshot

Frequency of sodium channel genotypes and association with pyrethrum knockdown time in populations of Californian Aedes aegypti

inferred← citeshttps://doi.org/10.1186/s13071-021-04785-4openalex-snapshot

Dengue fever and insecticide resistance in Aedes mosquitoes in Southeast Asia: a review

inferred← citeshttps://doi.org/10.1186/s13071-021-04867-3openalex-snapshot

Voltage-sensitive sodium channel (Vssc) mutations associated with pyrethroid insecticide resistance in Aedes aegypti (L.) from two districts of Jeddah, Kingdom of Saudi Arabia: baseline information for a Wolbachia release program

inferred← citeshttps://doi.org/10.1186/s13071-022-05192-zopenalex-snapshot

Knockdown resistance (kdr) gene of Aedes aegypti in Malaysia with the discovery of a novel regional specific point mutation A1007G

inferred← citeshttps://doi.org/10.1186/s13071-023-05743-yopenalex-snapshot

Association of 410L, 1016I and 1534C kdr mutations with pyrethroid resistance in Aedes aegypti from Ouagadougou, Burkina Faso, and development of a one-step multiplex PCR method for the simultaneous detection of 1534C and 1016I kdr mutations

inferred← citeshttps://doi.org/10.1186/s13071-023-05752-xopenalex-snapshot

Insecticide resistance status of Aedes aegypti in southern and northern Ghana

inferred← citeshttps://doi.org/10.1186/s13071-023-06066-8openalex-snapshot

First report of kdr mutations in the voltage-gated sodium channel gene in the arbovirus vector, Aedes aegypti, from Nouakchott, Mauritania

inferred← citeshttps://doi.org/10.1186/s13071-024-06123-wopenalex-snapshot

Kdr genotyping and the first report of V410L and V1016I kdr mutations in voltage-gated sodium channel gene in Aedes aegypti (Diptera: Culicidae) from Iran

inferred← citeshttps://doi.org/10.1186/s13071-024-06405-3openalex-snapshot

First detection of V410L kdr mutation in Aedes aegypti populations of Argentina supported by toxicological evidence

inferred← citeshttps://doi.org/10.1186/s13071-025-06943-4openalex-snapshot

Association of knockdown resistance mutations with pyrethroid resistance in Aedes aegypti, a major arbovirus vector in Cameroon

inferred← citeshttps://doi.org/10.1186/s13071-025-07010-8openalex-snapshot

Pyrethroid resistance in Aedes aegypti: genetic mechanisms worldwide, and recommendations for effective vector control

inferred← citeshttps://doi.org/10.1186/s13071-025-07083-5openalex-snapshot

Molecular characterization of invasive Aedes albopictus (Diptera: Culicidae) populations in northwest Iran: Insights into origin, insecticide resistance, and Wolbachia infection

inferred← citeshttps://doi.org/10.1186/s40249-020-00769-1openalex-snapshot

First detection of F1534C knockdown resistance mutation in Aedes aegypti (Diptera: Culicidae) from Cameroon

inferred← citeshttps://doi.org/10.1186/s40249-020-0637-2openalex-snapshot

Contrasting resistance patterns to type I and II pyrethroids in two major arbovirus vectors Aedes aegypti and Aedes albopictus in the Republic of the Congo, Central Africa

inferred← citeshttps://doi.org/10.1186/s40249-022-01013-8openalex-snapshot

Spatial distribution of insecticide resistant populations of Aedes aegypti and Ae. albopictus and first detection of V410L mutation in Ae. aegypti from Cameroon

inferred← citeshttps://doi.org/10.1186/s41182-025-00806-5openalex-snapshot

First report of the pyrethroid-resistance-associated V1016I mutation in Aedes aegypti at the seaport of Cotonou, Benin, West Africa

inferred← citeshttps://doi.org/10.1371/journal.pgen.1009606openalex-snapshot

Permethrin resistance in Aedes aegypti: Genomic variants that confer knockdown resistance, recovery, and death

inferred← citeshttps://doi.org/10.1371/journal.pntd.0006544openalex-snapshot

Quantification of permethrin resistance and kdr alleles in Florida strains of Aedes aegypti (L.) and Aedes albopictus (Skuse)

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007432openalex-snapshot

Molecular evidence of sequential evolution of DDT- and pyrethroid-resistant sodium channel in Aedes aegypti

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007439openalex-snapshot

Insecticide resistance levels and mechanisms in Aedes aegypti populations in and around Ouagadougou, Burkina Faso

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007624openalex-snapshot

Prolonged mosquitocidal activity of Siparuna guianensis essential oil encapsulated in chitosan nanoparticles

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007753openalex-snapshot

Loss of pyrethroid resistance in newly established laboratory colonies of Aedes aegypti

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007818openalex-snapshot

High-throughput genotyping of a full voltage-gated sodium channel gene via genomic DNA using target capture sequencing and analytical pipeline MoNaS to discover novel insecticide resistance mutations

inferred← citeshttps://doi.org/10.1371/journal.pntd.0007852openalex-snapshot

Distribution of insecticide resistance and mechanisms involved in the arbovirus vector Aedes aegypti in Laos and implication for vector control

inferred← citeshttps://doi.org/10.1371/journal.pntd.0008154openalex-snapshot

Evidence for both sequential mutations and recombination in the evolution of kdr alleles in Aedes aegypti

inferred← citeshttps://doi.org/10.1371/journal.pntd.0008216openalex-snapshot

The V410L knockdown resistance mutation occurs in island and continental populations of Aedes aegypti in West and Central Africa

inferred← citeshttps://doi.org/10.1371/journal.pntd.0008350openalex-snapshot

Tracing temporal and geographic distribution of resistance to pyrethroids in the arboviral vector Aedes albopictus

inferred← citeshttps://doi.org/10.1371/journal.pntd.0008492openalex-snapshot

Insecticide resistance and genetic structure of Aedes aegypti populations from Rio de Janeiro State, Brazil

inferred← citeshttps://doi.org/10.1371/journal.pntd.0009036openalex-snapshot

The entomological impact of passive metofluthrin emanators against indoor Aedes aegypti: A randomized field trial

inferred← citeshttps://doi.org/10.1371/journal.pntd.0009549openalex-snapshot

Levels of cross-resistance to pyrethroids conferred by the Vssc knockdown resistance allele 410L+1016I+1534C in Aedes aegypti

inferred← citeshttps://doi.org/10.1371/journal.pntd.0009746openalex-snapshot

Insecticide resistance in Aedes aegypti from Tapachula, Mexico: Spatial variation and response to historical insecticide use

inferred← citeshttps://doi.org/10.1371/journal.pntd.0009833openalex-snapshot

Kdr genotyping (V1016I, F1534C) of the Nav channel of Aedes aegypti (L.) mosquito populations in Harris County (Houston), Texas, USA, after Permanone 31–66 field tests and its influence on probability of survival

inferred← citeshttps://doi.org/10.1371/journal.pntd.0009871openalex-snapshot

Transcriptomic and proteomic analysis of pyrethroid resistance in the CKR strain of Aedes aegypti

inferred← citeshttps://doi.org/10.1371/journal.pntd.0010001openalex-snapshot

Molecular surveillance of resistance to pyrethroids insecticides in Colombian Aedes aegypti populations

inferred← citeshttps://doi.org/10.1371/journal.pntd.0010935openalex-snapshot

A next generation targeted amplicon sequencing method to screen for insecticide resistance mutations in Aedes aegypti populations reveals a rdl mutation in mosquitoes from Cabo Verde

inferred← citeshttps://doi.org/10.1371/journal.pntd.0011033openalex-snapshot

Impact of the V410L kdr mutation and co-occurring genotypes at kdr sites 1016 and 1534 in the VGSC on the probability of survival of the mosquito Aedes aegypti (L.) to Permanone in Harris County, TX, USA

inferred← citeshttps://doi.org/10.1371/journal.pntd.0011369openalex-snapshot

Pyrethroid susceptibility reversal in Aedes aegypti: A longitudinal study in Tapachula, Mexico

inferred← citeshttps://doi.org/10.1371/journal.pntd.0011397openalex-snapshot

Entomological surveillance on Aedes aegypti during covid 19 period in Cape Coast, Ghana: Risk of arboviral outbreaks, multiple insecticide resistance and distribution of F1534C, V410L and V1016I kdr mutations

inferred← citeshttps://doi.org/10.1371/journal.pntd.0011741openalex-snapshot

Fitness costs in the presence and absence of insecticide use explains abundance of two common Aedes aegypti kdr resistance alleles found in the Americas

inferred← citeshttps://doi.org/10.1371/journal.pntd.0012138openalex-snapshot

Three years of insecticide resistance evolution and associated mechanisms in Aedes aegypti populations of Ouagadougou, Burkina Faso

inferred← citeshttps://doi.org/10.1371/journal.pntd.0012768openalex-snapshot

First detection of the S989P+V1016G+D1763Y haplotype and expansion of voltage-gated sodium channel mutations in Aedes aegypti in Taiwan in 2016–2023

inferred← citeshttps://doi.org/10.1371/journal.pntd.0014393openalex-snapshot

Discovery of two novel mutations, R52H and N868D, in the voltage-gated sodium channel of Aedes aegypti associated with pyrethroid resistance

inferred← citeshttps://doi.org/10.1371/journal.pone.0196410openalex-snapshot

Pyrethroid insecticides maintain repellent effect on knock-down resistant populations of Aedes aegypti mosquitoes

inferred← citeshttps://doi.org/10.1371/journal.pone.0212693openalex-snapshot

Widespread insecticide resistance in Aedes aegypti L. from New Mexico, U.S.A.

inferred← citeshttps://doi.org/10.1371/journal.pone.0228695openalex-snapshot

Mechanisms associated with pyrethroid resistance in populations of Aedes aegypti (Diptera: Culicidae) from the Caribbean coast of Colombia

inferred← citeshttps://doi.org/10.1371/journal.pone.0243992openalex-snapshot

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

inferred← citeshttps://doi.org/10.1371/journal.pone.0278779openalex-snapshot

Spatial distribution and insecticide resistance profile of Aedes aegypti and Aedes albopictus in Douala, the most important city of Cameroon

inferred← citeshttps://doi.org/10.1371/journal.pone.0304550openalex-snapshot

First report of V1016I, F1534C and V410L kdr mutations associated with pyrethroid resistance in Aedes aegypti populations from Niamey, Niger

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/10.1590/0074-02760220210openalex-snapshot

Insecticide resistance levels and associated mechanisms in three Aedes aegypti populations from Venezuela

inferred← citeshttps://doi.org/10.1590/1806-9665-rbent-2023-0047openalex-snapshot

Genetic diversity and Kdr mutations of natural Aedes (Stegomyia) aegypti (Diptera: Culicidae) populations of Brazil

inferred← citeshttps://doi.org/10.21203/rs.3.rs-102568/v1openalex-snapshot

Molecular Insight into the Knockdown Resistance (kdr) in the Voltage Gated Sodium Channel (vgsc) Gene of the Main Dengue Vector, Aedes aegypti (Diptera: Culicidae) and the Discovery of Novel Regional Specific Point Mutation A1007G in Malaysia.

inferred← citeshttps://doi.org/10.21203/rs.3.rs-102568/v2openalex-snapshot

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1979481/v1openalex-snapshot

inferred← citeshttps://doi.org/10.21203/rs.3.rs-855427/v1openalex-snapshot

Predatory Abilities of The Backswimmer Buenoa Amnigenus Are Not Impaired After Sublethal Exposures To Pyriproxyfen

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/10.24252/diversity.v2i2.26283openalex-snapshot

Larvicidal Efficacy of Citrus amblycarpa Peel Extract Against the Larvae of Aedes albopictus

inferred← citeshttps://doi.org/10.3233/web-200437openalex-snapshot

Intelligent detection method for abnormal big data in heterogeneous networks based on Bayesian classification

inferred← citeshttps://doi.org/10.32473/jfmca.71.1.135292openalex-snapshot

NEW MULTIPLEX SNP GENOTYPING ASSAY TO SIMUTANEOUSLY SCREEN FOR EIGHT VOLTAGE-GATED SODIUM CHANNEL MUTATIONS IN AEDES AEGYPTI

inferred← citeshttps://doi.org/10.32473/jfmca.v69i1.130622openalex-snapshot

TWO NOVEL SINGLE NUCLEOTIDE POLYMORPHISMS IN THE VOLTAGE-GATED SODIUM CHANNEL GENE IDENTIFIED IN AEDES AEGYPTI MOSQUITOES FROM FLORIDA

inferred← citeshttps://doi.org/10.3389/fpls.2021.685864openalex-snapshot

Larvicidal Activity of Essential Oils From Piper Species Against Strains of Aedes aegypti (Diptera: Culicidae) Resistant to Pyrethroids

inferred← citeshttps://doi.org/10.3389/fpubh.2026.1754455openalex-snapshot

Rising of pyrethroid resistance mutations (kdr) in the dengue vector Aedes aegypti from northeastern Argentina

inferred← citeshttps://doi.org/10.3390/bioengineering8070092openalex-snapshot

Bioremediation of Agricultural Soils Polluted with Pesticides: A Review

inferred← citeshttps://doi.org/10.3390/genes12060828openalex-snapshot

Analyses of Insecticide Resistance Genes in Aedes aegypti and Aedes albopictus Mosquito Populations from Cameroon

inferred← citeshttps://doi.org/10.3390/genes17080854openalex-snapshot

RNAi-Mediated Knockdown of the Sodium Channel Auxiliary Subunit TipE Increases Pyrethroid-Associated Mortality and Reveals Metabolic Transcriptional Responses in Megalurothrips usitatus

inferred← citeshttps://doi.org/10.3390/ijms26051854openalex-snapshot

Omics Approaches in Understanding Insecticide Resistance in Mosquito Vectors

inferred← citeshttps://doi.org/10.3390/insects12010071openalex-snapshot

Permethrin Resistance in Aedes aegypti Affects Aspects of Vectorial Capacity

inferred← citeshttps://doi.org/10.3390/insects12100917openalex-snapshot

Implications of Sublethal Insecticide Exposure and the Development of Resistance on Mosquito Physiology, Behavior, and Pathogen Transmission

inferred← citeshttps://doi.org/10.3390/insects13020187openalex-snapshot

Temporal Evaluation of Insecticide Resistance in Populations of the Major Arboviral Vector Aedes Aegypti from Northern Nigeria

inferred← citeshttps://doi.org/10.3390/insects14010031openalex-snapshot

Spatial Distribution of Pyrethroid Resistance and kdr Mutations in Aedes aegypti from La Guajira, Colombia

inferred← citeshttps://doi.org/10.3390/insects15120998openalex-snapshot

Preparation of β-Myrcene-Chitosan Nanoparticles and Their Uptake and Toxicity in Aedes aegypti Larvae

inferred← citeshttps://doi.org/10.3390/insects16030254openalex-snapshot

Assessing Temperature-Dependent Deltamethrin Toxicity in Various kdr Genotypes of Aedes aegypti Mosquitoes

inferred← citeshttps://doi.org/10.3390/insects16040435openalex-snapshot

Diflubenzuron Did Not Affect the Abilities of the Backswimmer Buenoa tarsalis to Survive and Prey Upon Larvae of Aedes aegypti

inferred← citeshttps://doi.org/10.3390/insects16060551openalex-snapshot

Detection of Di- and Tri-Locus kdr Mutations in Aedes aegypti and Aedes albopictus from Texas, USA, and the Implications for Insecticide Resistance

inferred← citeshttps://doi.org/10.3390/insects17050510openalex-snapshot

Pepper Constituents Enhance the Toxicity and Neurophysiological Effects of Natural Pyrethrins in Insects

inferred← citeshttps://doi.org/10.3390/insects17060573openalex-snapshot

Susceptibility to Beta-Cypermethrin, the F1534C Mutation, and MFO Amount in Aedes aegypti from Dengue-Endemic Areas of Yunnan Province, China, in 2015–2016

inferred← citeshttps://doi.org/10.3390/insects17101029openalex-snapshot

Characterization of a Stably Maintained, Highly Beta-Cypermethrin-Resistant Strain of the Bird Cherry-Oat Aphid Rhopalosiphum padi (Hemiptera: Aphididae)

inferred← citeshttps://doi.org/10.3390/insects9010023openalex-snapshot

A Point Mutation V419L in the Sodium Channel Gene from Natural Populations of Aedes aegypti Is Involved in Resistance to λ-Cyhalothrin in Colombia

inferred← citeshttps://doi.org/10.3390/insects9030109openalex-snapshot

Evaluation of Eosin-Methylene Blue as a Photosensitizer for Larval Control of Aedes aegypti by a Photodynamic Process

inferred← citeshttps://doi.org/10.3390/molecules31122098openalex-snapshot

Developmental Consequences of Early-Life Exposure and Adulticidal Effects of Siparuna Species Essential Oils in Aedes aegypti

inferred← citeshttps://doi.org/10.3390/plants11233298openalex-snapshot

Methanolic Extracts of Chiococca alba in Aedes aegypti Biorational Management: Larvicidal and Repellent Potential, and Selectivity against Non-Target Organisms

inferred← citeshttps://doi.org/10.3390/plants14091322openalex-snapshot

Siparuna gesnerioides and Siparuna guianensis Essential Oils in Aedes aegypti Control: Phytoanalysis, Molecular Insights for Larvicidal Activity and Selectivity to Non-Target Organisms

inferred← citeshttps://doi.org/10.3390/toxics13080681openalex-snapshot

Mechanisms and Genetic Drivers of Resistance of Insect Pests to Insecticides and Approaches to Its Control

inferred← citeshttps://doi.org/10.3390/toxins17080402openalex-snapshot

Phytochemistry, Mode of Action Predictions, and Synergistic Potential of Hypenia irregularis Essential Oil Mixtures for Controlling Aedes aegypti

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/10.5772/intechopen.81439openalex-snapshot

Ecology of Aedes Mosquitoes, the Major Vectors of Arboviruses in Human Population

inferred← citeshttps://doi.org/10.6084/m9.figshare.12344981openalex-snapshot

Additional file 1 of Evaluation of resistance to pyrethroid and organophosphate adulticides and kdr genotyping in Aedes aegypti populations from Roraima, the northernmost Brazilian State

inferred← citeshttps://doi.org/10.6084/m9.figshare.12986737openalex-snapshot

Additional file 1 of Surveillance of Aedes aegypti populations in the city of Praia, Cape Verde: Zika virus infection, insecticide resistance and genetic diversity

inferred← citeshttps://doi.org/10.6084/m9.figshare.12986740openalex-snapshot

Additional file 2 of Surveillance of Aedes aegypti populations in the city of Praia, Cape Verde: Zika virus infection, insecticide resistance and genetic diversity

inferred← citeshttps://doi.org/10.6084/m9.figshare.12986743openalex-snapshot

Additional file 3 of Surveillance of Aedes aegypti populations in the city of Praia, Cape Verde: Zika virus infection, insecticide resistance and genetic diversity

inferred← citeshttps://doi.org/10.6084/m9.figshare.12986746openalex-snapshot

Additional file 4 of Surveillance of Aedes aegypti populations in the city of Praia, Cape Verde: Zika virus infection, insecticide resistance and genetic diversity

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