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Resistencia a insecticidas en Aedes aegypti y Aedes albopictus (Diptera: Culicidae) de Tapachula, Chiapas, México
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/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.yrtph.2012.12.010openalex-snapshot
Absorption and excretion of organophosphorous insecticide biomarkers of malathion in the rat: Implications for overestimation bias and exposure misclassification from environmental biomonitoring
inferredcites →https://doi.org/10.1016/s0965-1748(04)00069-4openalex-snapshot
The molecular basis of insecticide resistance in mosquitoes
inferredcites →https://doi.org/10.1093/jmedent/42.5.821openalex-snapshot
Insecticide Susceptibility ofAedes aegyptiandAedes albopictusacross Thailand
inferredcites →https://doi.org/10.1186/1475-2875-7-168openalex-snapshot
Multiple insecticide resistance mechanisms involving metabolic changes and insensitive target sites selected in anopheline vectors of malaria in Sri Lanka
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.0003771openalex-snapshot
Transcriptome Profiling and Genetic Study Reveal Amplified Carboxylesterase Genes Implicated in Temephos Resistance, in the Asian Tiger Mosquito Aedes albopictus
inferredcites →https://doi.org/10.1371/journal.pone.0101992openalex-snapshot
Insecticide Resistance Status of United States Populations of Aedes albopictus and Mechanisms Involved
inferredcites →https://doi.org/10.1590/s0074-02762004000200015openalex-snapshot
Aedes aegypti resistance to temephos during 2001 in several municipalities in the states of Rio de Janeiro, Sergipe, and Alagoas, Brazil
inferredcites →https://doi.org/10.1603/0022-2585-41.5.946openalex-snapshot
Insecticide Resistance in Alabama and Florida Mosquito Strains ofAedes albopictus
inferredcites →https://doi.org/10.2149/tmh.2011-s04openalex-snapshot
Dengue Vectors and their Spatial Distribution
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/10.3958/059.039.0307openalex-snapshot
Natural Transmission of Dengue Virus by Aedes albopictus at Monterrey, Northeastern Mexico
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/s00438-024-02185-8openalex-snapshot
Comparative transcriptional analysis between susceptible and resistant populations of Aedes (Stegomyia) aegypti (Linnaeus, 1762) after malathion exposure
inferred← citeshttps://doi.org/10.1007/s10340-025-01953-8openalex-snapshot
Aromatic plant–insect dynamics: molecular insights for advancing pest control strategies
inferred← citeshttps://doi.org/10.1007/s10526-024-10292-zopenalex-snapshot
Effect of melanization of entomopathogenic nematodes on the potential of Steinernema feltiae and Heterorhabditis bacteriophora for the control of Aedes albopictus and Aedes aegypti
inferred← citeshttps://doi.org/10.1007/s10653-023-01618-4openalex-snapshot
The situation of chlorpyrifos in Mexico: a case study in environmental samples and aquatic organisms
inferred← citeshttps://doi.org/10.1007/s42690-026-01841-3openalex-snapshot
Expanding the arsenal: non-conventional insecticides for managing pyrethroid-resistant Aedes aegypti
inferred← citeshttps://doi.org/10.1016/j.jip.2025.108468openalex-snapshot
Wolbachia-Based Biocontrol of Aedes aegypti: Current Progress, Challenges, and Future Prospects
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/10.1186/s41182-024-00637-wopenalex-snapshot
Insecticide resistance status and mechanisms in Aedes aegypti and Aedes albopictus from different dengue endemic regions of Panama
inferred← citeshttps://doi.org/10.1186/s41182-026-01054-xopenalex-snapshot
Insecticide resistance in larval populations of Aedes aegypti and Aedes albopictus from Panama
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/10.14482/sun.38.3.614.58openalex-snapshot
Conocimientos y factores de riesgo socioambientales en relación con arbovirosis urbanas en Barranquilla (Colombia)
inferred← citeshttps://doi.org/10.1590/s1678-9946202466062openalex-snapshot
Mutations in the voltage-gated sodium channel associated with pyrethroid resistance in Aedes albopictus in Yucatan, Mexico
inferred← citeshttps://doi.org/10.1653/024.105.0312openalex-snapshot
Susceptibility Status to Temephos in Larval Aedes aegypti and Aedes albopictus (Diptera: Culicidae) Populations from Quintana Roo, Southeastern Mexico
inferred← citeshttps://doi.org/10.18474/jes22-32openalex-snapshot
Larval Emergence from Aedes aegypti (Diptera: Culicidae) Eggs Exposed to Hot Air
inferred← citeshttps://doi.org/10.21640/ns.v13i27.2840openalex-snapshot
Extracto de Acacia farnesiana para el control de larva de Aedes aegypti
inferred← citeshttps://doi.org/10.31790/inspilip.v6i1.264openalex-snapshot
Resistencia a insecticidas en poblaciones de Aedes aegypti en la provincia de Manabí, Ecuador
inferred← citeshttps://doi.org/10.3390/insects14060565openalex-snapshot
Aedes aegypti, Ae. albopictus and Culex quinquefasciatus Adults Found Coexisting in Urban and Semiurban Dwellings of Southern Chiapas, Mexico
inferred← citeshttps://doi.org/10.3390/insects15020120openalex-snapshot
Widespread Resistance to Temephos in Aedes aegypti (Diptera: Culicidae) from Mexico
inferred← citeshttps://doi.org/10.3390/insects17030264openalex-snapshot
Current Knowledge on Insecticide Resistance in Aedes albopictus (Skuse, 1894) in Latin America and the Caribbean Nations
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/10.3390/tropicalmed11050134openalex-snapshot
Oviposition Deterrent and Larvicidal Activity of Salvia munzii Essential Oil Against Susceptible and Insecticide-Resistant Aedes aegypti
inferred← citeshttps://doi.org/10.3390/tropicalmed9080184openalex-snapshot
Repurposing Insecticides for Mosquito Control: Evaluating Spiromesifen, a Lipid Synthesis Inhibitor against Aedes aegypti (L.)
inferred← citeshttps://doi.org/10.35366/121147openalex-snapshot
Dengue: estado actual de una enfermedad recurrente en México
inferred← citeshttps://doi.org/10.4236/ae.2022.103018openalex-snapshot
Comparison of Insecticide Resistance and Its Enzyme Mechanisms among Aedes aegypti Collected with Three Methods in a Dengue-Endemic City in Southern Mexico
inferred← citeshttps://doi.org/10.4269/ajtmh.22-0707openalex-snapshot
House Condition Scoring Scale as a Risk Indicator of Infestation by Aedes in Two Mexican Localities
inferred← citeshttps://doi.org/10.56712/latam.v6i2.3660openalex-snapshot
Resistencia a insecticidas del mosquito Aedes aegypti en los cantones de la Provincia de Manabí – Ecuador durante el periodo 2020-2024. Revisión bibliográfica
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