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

https://doi.org/10.1371/journal.pntd.0008154
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ps.3846openalex-snapshot
Frequency of V1016I and F1534C mutations in the voltage‐gated sodium channel gene in Aedes aegypti in Venezuela
inferredcites →https://doi.org/10.1002/ps.4771openalex-snapshot
Voltage‐sensitive sodium channel mutations S989P + V1016G in Aedes aegypti confer variable resistance to pyrethroids, DDT and oxadiazines
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/s12686-011-9548-7openalex-snapshot
STRUCTURE HARVESTER: a website and program for visualizing STRUCTURE output and implementing the Evanno method
inferredcites →https://doi.org/10.1016/j.actatropica.2008.08.004openalex-snapshot
Development and application of a simple colorimetric assay reveals widespread distribution of sodium channel mutations in Thai populations of Aedes aegypti
inferredcites →https://doi.org/10.1016/j.actatropica.2015.04.026openalex-snapshot
Involvement of metabolic resistance and F1534C kdr mutation in the pyrethroid resistance mechanisms of Aedes aegypti in India
inferredcites →https://doi.org/10.1016/j.actatropica.2018.12.021openalex-snapshot
Mechanisms of pyrethroid resistance in Aedes (Stegomyia) aegypti from Colombia
inferredcites →https://doi.org/10.1016/j.ibmb.2004.12.004openalex-snapshot
Evidence for multiple origins of identical insecticide resistance mutations in the aphid Myzus persicae
inferredcites →https://doi.org/10.1016/j.ibmb.2005.10.007openalex-snapshot
Multiple origins of pyrethroid resistance in sympatric biotypes of Bemisia tabaci (Hemiptera: Aleyrodidae)
inferredcites →https://doi.org/10.1016/j.ibmb.2009.01.001openalex-snapshot
A novel amino acid substitution in a voltage-gated sodium channel is associated with knockdown resistance to permethrin in Aedes aegypti
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.pestbp.2009.10.005openalex-snapshot
A novel F1552/C1552 point mutation in the Aedes aegypti voltage-gated sodium channel gene associated with permethrin resistance
inferredcites →https://doi.org/10.1016/j.pestbp.2012.08.001openalex-snapshot
Multiple evolutionary origins of knockdown resistance (kdr) in pyrethroid-resistant Colorado potato beetle, Leptinotarsa decemlineata
inferredcites →https://doi.org/10.1016/j.pestbp.2013.07.005openalex-snapshot
The pyrethroid resistance status and mechanisms in Aedes aegypti from the Guerrero state, Mexico
inferredcites →https://doi.org/10.1016/j.pestbp.2013.10.006openalex-snapshot
Insecticide resistance in house flies from the United States: Resistance levels and frequency of pyrethroid resistance alleles
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.pestbp.2017.08.013openalex-snapshot
Two novel house fly Vssc mutations, D600N and T929I, give rise to new insecticide resistance alleles
inferredcites →https://doi.org/10.1016/j.pestbp.2019.04.006openalex-snapshot
Insecticide resistance monitoring of house fly populations from the United States
inferredcites →https://doi.org/10.1016/s1473-3099(16)00146-8openalex-snapshot
The global economic burden of dengue: a systematic analysis
inferredcites →https://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
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/10.1046/j.1365-2915.2003.00412.xopenalex-snapshot
Pyrethroid and DDT cross‐resistance in Aedes aegypti is correlated with novel mutations in the voltage‐gated sodium channel gene
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.01020.xopenalex-snapshot
TCS: a computer program to estimate gene genealogies
inferredcites →https://doi.org/10.1046/j.1471-8286.2003.00566.xopenalex-snapshot
distruct : a program for the graphical display of population structure
inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
inferredcites →https://doi.org/10.1093/bioinformatics/btm233openalex-snapshot
CLUMPP: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure
inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
inferredcites →https://doi.org/10.1093/biosci/biy119openalex-snapshot
Recent History of Aedes aegypti : Vector Genomics and Epidemiology Records
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/jme/tjx143openalex-snapshot
Resistance Status and Resistance Mechanisms in a Strain of Aedes aegypti (Diptera: Culicidae) From Puerto Rico
inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot
jModelTest: Phylogenetic Model Averaging
inferredcites →https://doi.org/10.1111/2041-210x.12410openalex-snapshot
popart : full‐feature software for haplotype network construction
inferredcites →https://doi.org/10.1111/evo.12281openalex-snapshot
HUMAN IMPACTS HAVE SHAPED HISTORICAL AND RECENT EVOLUTION IN AEDES AEGYPTI , THE DENGUE AND YELLOW FEVER MOSQUITO
inferredcites →https://doi.org/10.1111/imb.12605openalex-snapshot
Conservation of the voltage‐sensitive sodium channel protein within the Insecta
inferredcites →https://doi.org/10.1111/j.1365-2583.2006.00620.xopenalex-snapshot
Frequencies of the pyrethroid resistance alleles of Vssc1 and CYP6D1 in house flies from the eastern United States
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.1365-2915.2012.01048.xopenalex-snapshot
Proof of concept for a novel insecticide bioassay based on sugar feeding by adult Aedes aegypti ( Stegomyia aegypti )
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02553.xopenalex-snapshot
Detecting the number of clusters of individuals using the software structure : a simulation study
inferredcites →https://doi.org/10.1111/j.1365-3156.2009.02378.xopenalex-snapshot
Frequency of Val1016Ile mutation in the voltage‐gated sodium channel gene of Aedes aegypti Brazilian populations
inferredcites →https://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
inferredcites →https://doi.org/10.1111/mec.13866openalex-snapshot
Global genetic diversity of Aedes aegypti
inferredcites →https://doi.org/10.1146/annurev-ento-011118-112420openalex-snapshot
Life and Death at the Voltage-Sensitive Sodium Channel: Evolution in Response to Insecticide Use
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/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/s13071-015-0933-zopenalex-snapshot
Relationship between insecticide resistance and kdr mutations in the dengue vector Aedes aegypti in Southern China
inferredcites →https://doi.org/10.1186/s13071-017-2096-6openalex-snapshot
Combined target site (kdr) mutations play a primary role in highly pyrethroid resistant phenotypes of Aedes aegypti from Saudi Arabia
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/s13071-018-3113-0openalex-snapshot
First report of V1016G and S989P knockdown resistant (kdr) mutations in pyrethroid-resistant Sri Lankan Aedes aegypti mosquitoes
inferredcites →https://doi.org/10.1186/s13071-018-3275-9openalex-snapshot
Fine-scale spatial and temporal dynamics of kdr haplotypes in Aedes aegypti from Mexico
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/s13071-019-3472-1openalex-snapshot
Enzymatic and molecular characterization of insecticide resistance mechanisms in field populations of Aedes aegypti from Selangor, Malaysia
inferredcites →https://doi.org/10.1186/s41182-018-0134-5openalex-snapshot
High frequencies of F1534C and V1016I kdr mutations and association with pyrethroid resistance in Aedes aegypti from Somgandé (Ouagadougou), Burkina Faso
inferredcites →https://doi.org/10.12688/f1000research.8107.1openalex-snapshot
Surveillance, insecticide resistance and control of an invasive Aedes aegypti (Diptera: Culicidae) population in California
inferredcites →https://doi.org/10.12688/f1000research.8107.3openalex-snapshot
Surveillance, insecticide resistance and control of an invasive Aedes aegypti (Diptera: Culicidae) population in California
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.pntd.0000391openalex-snapshot
Nationwide Investigation of the Pyrethroid Susceptibility of Mosquito Larvae Collected from Used Tires in Vietnam
inferredcites →https://doi.org/10.1371/journal.pntd.0000531openalex-snapshot
Recent Rapid Rise of a Permethrin Knock Down Resistance Allele in Aedes aegypti in México
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.0003032openalex-snapshot
Co-occurrence of Point Mutations in the Voltage-Gated Sodium Channel of Pyrethroid-Resistant Aedes aegypti Populations in Myanmar
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.0003332openalex-snapshot
Pyrethroid-Resistance and Presence of Two Knockdown Resistance (kdr) Mutations, F1534C and a Novel Mutation T1520I, in Indian Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pntd.0004263openalex-snapshot
Coevolution of the Ile1,016 and Cys1,534 Mutations in the Voltage Gated Sodium Channel Gene of Aedes aegypti in Mexico
inferredcites →https://doi.org/10.1371/journal.pntd.0004780openalex-snapshot
Discovery of Point Mutations in the Voltage-Gated Sodium Channel from African Aedes aegypti Populations: Potential Phylogenetic Reasons for Gene Introgression
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.0006544openalex-snapshot
Quantification of permethrin resistance and kdr alleles in Florida strains of Aedes aegypti (L.) and Aedes albopictus (Skuse)
inferredcites →https://doi.org/10.1371/journal.pntd.0006734openalex-snapshot
Laboratory selection of Aedes aegypti field populations with the organophosphate malathion: Negative impacts on resistance to deltamethrin and to the organophosphate temephos
inferredcites →https://doi.org/10.1371/journal.pntd.0007291openalex-snapshot
Voltage-gated sodium channel intron polymorphism and four mutations comprise six haplotypes in an Aedes aegypti population in Taiwan
inferredcites →https://doi.org/10.1371/journal.pntd.0007439openalex-snapshot
Insecticide resistance levels and mechanisms in Aedes aegypti populations in and around Ouagadougou, Burkina Faso
inferredcites →https://doi.org/10.1371/journal.pone.0052761openalex-snapshot
Multiple Origins of kdr-type Resistance in the House Fly, Musca domestica
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/10.1371/journal.pone.0179673openalex-snapshot
Insecticide resistance to permethrin and malathion and associated mechanisms in Aedes aegypti mosquitoes from St. Andrew Jamaica
inferredcites →https://doi.org/10.1371/journal.pone.0212693openalex-snapshot
Widespread insecticide resistance in Aedes aegypti L. from New Mexico, U.S.A.
inferredcites →https://doi.org/10.1371/journal.pone.0215541openalex-snapshot
Prevalence of kdr mutations and insecticide susceptibility among natural population of Aedes aegypti in West Bengal
inferredcites →https://doi.org/10.1590/s1984-46702015000100003openalex-snapshot
Insecticide resistance and genetic variability in natural populations of Aedes (Stegomyia) aegypti (Diptera: Culicidae) from Colombia
inferredcites →https://doi.org/10.1603/me10152openalex-snapshot
Early History of Laboratory Breeding of Aedes aegypti (Diptera: Culicidae) Focusing on the Origins and Use of Selected Strains
inferredcites →https://doi.org/10.18585/inabj.v10i3.425openalex-snapshot
Detection of Polymorphism on Voltage-gated Sodium Channel Gene of Indonesian Aedes aegypti Associated with Resistance to Pyrethroids
inferredcites →https://doi.org/10.3390/insects6030608openalex-snapshot
Repellency of Plant Extracts against the Legume Flower Thrips Megalurothrips sjostedti (Thysanoptera: Thripidae)
inferredcites →https://doi.org/10.3390/insects6030658openalex-snapshot
Association between Three Mutations, F1565C, V1023G and S996P, in the Voltage-Sensitive Sodium Channel Gene and Knockdown Resistance in Aedes aegypti from Yogyakarta, Indonesia
inferredcites →https://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
inferredcites →https://doi.org/10.3390/insects9020043openalex-snapshot
Susceptibility Status and Resistance Mechanisms in Permethrin-Selected, Laboratory Susceptible and Field-Collected Aedes aegypti from Malaysia
inferredcites →https://doi.org/10.4269/ajtmh.2010.09-0623openalex-snapshot
Pyrethroid Resistance in Aedes aegypti from Grand Cayman

What points at this work

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

inferred← citeshttps://doi.org/10.6620/zs.2025.64-31zenodo-depositor-declared
Understanding the Global Dynamics of Pyrethroid Resistance-related kdr mutations in Aedes (Stegomyia) aegypti (Linnaeus, 1762) (Diptera: Culicidae).
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.6306openalex-snapshot
Fitness studies of insecticide resistant strains: lessons learned and future directions
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.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/10.1007/s00436-025-08538-5openalex-snapshot
Pyrethroid and organochlorine susceptibility in Aedes aegypti populations from eastern black sea region, Türkiye: traces in the kdr gene region of the species origin
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.cois.2023.101134openalex-snapshot
The loci of insect phenotypic evolution
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.pestbp.2023.105577openalex-snapshot
Insecticide resistance: Status and potential mechanisms in Aedes aegypti
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.2025.106832openalex-snapshot
Challenges in insecticide resistance management: Implications of alternating selection in the yellow fever mosquito, Aedes aegypti
inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106843openalex-snapshot
Nationwide integrative analysis of pyrethroid resistance in Aedes aegypti from Mexico
inferred← citeshttps://doi.org/10.1021/acsomega.5c11595openalex-snapshot
Molecular and Biochemical Characterization of Insecticide Resistance in Field-Caught Aedes aegypti from Al-Madinah Al-Munawarah, Saudi Arabia
inferred← citeshttps://doi.org/10.1038/s41467-024-49792-yopenalex-snapshot
Global, asynchronous partial sweeps at multiple insecticide resistance genes in Aedes mosquitoes
inferred← citeshttps://doi.org/10.1038/s41598-020-70029-7openalex-snapshot
Kdr genotyping in Aedes aegypti from Brazil on a nation-wide scale from 2017 to 2018
inferred← citeshttps://doi.org/10.1038/s41598-021-83465-wopenalex-snapshot
Insecticide resistance and underlying targets-site and metabolic mechanisms in Aedes aegypti and Aedes albopictus from Lahore, Pakistan
inferred← citeshttps://doi.org/10.1038/s41598-024-60555-zopenalex-snapshot
A mathematical model for mapping the insecticide resistance trend in the Anopheles gambiae mosquito population under climate variability in Africa
inferred← citeshttps://doi.org/10.1038/s41598-024-64007-6openalex-snapshot
Uncovering the genetic diversity in Aedes aegypti insecticide resistance genes through global comparative genomics
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/10.1093/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/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/tjae115openalex-snapshot
Widespread geographic distribution of Aedes aegypti (Diptera: Culicidae) kdr variants in Panama
inferred← citeshttps://doi.org/10.1093/jme/tjaf195openalex-snapshot
Molecular detection of insecticide resistance markers in Aedes aegypti (Diptera: Culicidae) populations from Haiti
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/10.1101/2024.03.07.584008openalex-snapshot
Demographic history and the efficacy of selection in the globally invasive mosquito Aedes aegypti
inferred← citeshttps://doi.org/10.1101/2024.04.09.588653openalex-snapshot
Global, asynchronous partial sweeps at multiple insecticide resistance genes in Aedes mosquitoes
inferred← citeshttps://doi.org/10.1101/2024.12.11.627862openalex-snapshot
Knockdown-resistance ( kdr ) mutations in Indian Aedes aegypti populations: lack of recombination among haplotypes bearing V1016G, F1534C, and F1534L kdr alleles
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/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/10.1126/sciadv.abq7345openalex-snapshot
Discovery of super–insecticide-resistant dengue mosquitoes in Asia: Threats of concomitant knockdown resistance mutations
inferred← citeshttps://doi.org/10.1186/s12915-023-01693-0openalex-snapshot
The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.1186/s12920-025-02165-wopenalex-snapshot
Influence of genetic factors of humans, mosquitoes and parasites, on the evolution of Plasmodium falciparum infections, malaria transmission and genetic control methods: a review of the literature
inferred← citeshttps://doi.org/10.1186/s12936-024-05069-9openalex-snapshot
Longitudinal survey of insecticide resistance in a village of central region of Burkina Faso reveals co-occurrence of 1014F, 1014S and 402L mutations in Anopheles coluzzii and Anopheles arabiensis
inferred← citeshttps://doi.org/10.1186/s13071-018-3275-9openalex-snapshot
Fine-scale spatial and temporal dynamics of kdr haplotypes in Aedes aegypti from Mexico
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/s13071-022-05192-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/s13071-023-06066-8openalex-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/s13071-024-06124-9openalex-snapshot
Pyrethroid resistance status and co-occurrence of V1016G, F1534C and S989P mutations in the Aedes aegypti population from two dengue outbreak counties along the China-Myanmar border
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/s13071-024-06547-4openalex-snapshot
Monitoring of pyrethroid resistance in Aedes aegypti: first report of double and triple kdr mutations in Buenos Aires Province
inferred← citeshttps://doi.org/10.1186/s13071-025-06817-9openalex-snapshot
Global distribution and impact of knockdown resistance mutations in Aedes aegypti on pyrethroid resistance
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/s13071-026-07619-3openalex-snapshot
Insecticide susceptibility and knockdown resistance (Kdr) mutations (F1534C and V1016I) in Aedes aegypti populations from Dar es Salaam, Tanzania
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.15974.2openalex-snapshot
Insecticide resistance selection and reversal in two strains of Aedes aegypti
inferred← citeshttps://doi.org/10.1371/journal.pntd.0009271openalex-snapshot
Fitness costs of individual and combined pyrethroid resistance mechanisms, kdr and CYP-mediated detoxification, in Aedes aegypti
inferred← citeshttps://doi.org/10.1371/journal.pntd.0009546openalex-snapshot
Sodium channel activation underlies transfluthrin repellency in Aedes aegypti
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.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.0010355openalex-snapshot
High DDT resistance without apparent association to kdr and Glutathione-S-transferase (GST) gene mutations in Aedes aegypti population at hotel compounds in Zanzibar
inferred← citeshttps://doi.org/10.1371/journal.pntd.0010780openalex-snapshot
The role of voltage-gated sodium channel genotypes in pyrethroid resistance in Aedes aegypti in Taiwan
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.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.0013126openalex-snapshot
Knockdown-resistance (kdr) mutations in Indian Aedes aegypti populations: Lack of recombination among haplotypes bearing V1016G, F1534C, and F1534L kdr alleles
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
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-4681871/v1openalex-snapshot
Monitoring of pyrethroid resistance in Aedes aegypti: first report of double and triple kdr mutations in Buenos Aires Province
inferred← citeshttps://doi.org/10.21203/rs.3.rs-9025253/v1openalex-snapshot
Resistance profiles and mechanisms in pyrethroid-resistant Aedes aegypti populations: first detection of the V1016G kdr mutation in Abidjan, Côte d’Ivoire
inferred← citeshttps://doi.org/10.21203/rs.3.rs-9690015/v1openalex-snapshot
Mosquito-borne pathogens and entomological outcomes in a high-risk setting: evidence from BG-Sentinel FTA surveillance in Djibouti
inferred← citeshttps://doi.org/10.2987/23-7160openalex-snapshot
Aedes aegypti Knockdown Resistance Mutations and Dengue Virus Infection in Haiti
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/fcimb.2023.1265873openalex-snapshot
Evolution of knockdown resistance (kdr) mutations of Aedes aegypti and Aedes albopictus in Hainan Island and Leizhou Peninsula, China
inferred← citeshttps://doi.org/10.3389/fgene.2022.867231openalex-snapshot
Genome-wide Association Study Reveals New Loci Associated With Pyrethroid Resistance in Aedes aegypti
inferred← citeshttps://doi.org/10.3390/insects12010071openalex-snapshot
Permethrin Resistance in Aedes aegypti Affects Aspects of Vectorial Capacity
inferred← citeshttps://doi.org/10.3390/insects15110863openalex-snapshot
Detection of the 1016Gly and 989Pro Knockdown Resistance Mutations in Florida, USA Aedes aegypti
inferred← citeshttps://doi.org/10.3390/insects16030288openalex-snapshot
Insecticide Resistance Status of Aedes aegypti Adults and Larvae in Nouakchott, Mauritania
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/10.55446/ije.2025.3408openalex-snapshot
Pyrethroid Resistance in Aedes aegypti L. across Southeast Asia: Mechanisms and Implications for Vector Control
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617204openalex-snapshot
Additional file 1 of The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617207openalex-snapshot
Additional file 2 of The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617210openalex-snapshot
Additional file 3 of The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.6084/m9.figshare.26685894openalex-snapshot
Additional file 1 of Pyrethroid resistance status and co-occurrence of V1016G, F1534C and S989P mutations in the Aedes aegypti population from two dengue outbreak counties along the China-Myanmar border
inferred← citeshttps://doi.org/10.6084/m9.figshare.26685897openalex-snapshot
Additional file 2 of Pyrethroid resistance status and co-occurrence of V1016G, F1534C and S989P mutations in the Aedes aegypti population from two dengue outbreak counties along the China-Myanmar border
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