FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2133661644> ?p ?o ?g. }

• W2133661644 endingPage "382" @default.
• W2133661644 startingPage "375" @default.
• W2133661644 abstract "A resistance management programme comparing rotations, mosaics and single use of insecticides for residual house-spraying against the insect vectors of malaria is being carried out in Southern Mexico. The area was chosen because of its prior history of insecticide use, relatively sedentary vector, and physical features of the area which limit inward migration of insects to the study area. A high level of resistance to DDT and low levels of organophosphorus (OP), carbamate and pyrethroid resistance were detected by WHO discriminating-dose assays in field populations of Anopheles albimanus in the pre-spray period in the region where this resistance management project is being undertaken. After the first year of spraying, resistance, as measured by a discriminating-dose assay, was still at a high level for DDT and had risen for all the other insecticides. Biochemical assays showed that DDT resistance was primarily caused by elevated levels of glutathione S-transferase (GST) activity leading to increased rates of metabolism of DDT to DDE. The numbers of individuals with elevated GST and DDT resistance were well correlated, suggesting that this is the only major DDT resistance mechanism in this population. The carbamate resistance in this population was conferred by an altered acetylcholinesterase (AChE) mechanism. The level of resistance in bioassays correlated well with the frequency of individuals homozygous for the altered AChE allele. This suggests that the level of resistance conferred by this mechanism in its heterozygous state is below the level of detection of the bioassay. The low levels of OP and pyrethroid resistance could be conferred by either the elevated esterase or monooxygenase enzymes. The esterases, however, are elevated only with p-nitrophenyl acetate (PNPA), and are unlikely to be causing broad-spectrum OP resistance. The altered AChE mechanism may also be contributing to the OP but not the pyrethroid resistance. There were significant differences in some resistance gene frequencies for insects obtained by different indoor and outdoor trapping methods. To determine whether the different sampling methods were effectively sampling the same interbreeding population, RAPD analysis of insects obtained by different collection methods in different villages was undertaken. There was no observed variability in the RAPD patterns for the different mosquito samples with a number of primers. ©1997 SCI" @default.
• W2133661644 created "2016-06-24" @default.
• W2133661644 creator A5017078169 @default.
• W2133661644 creator A5028559891 @default.
• W2133661644 creator A5041783872 @default.
• W2133661644 creator A5044985417 @default.
• W2133661644 creator A5067322954 @default.
• W2133661644 creator A5078298627 @default.
• W2133661644 creator A5083150936 @default.
• W2133661644 date "1997-11-01" @default.
• W2133661644 modified "2023-09-27" @default.
• W2133661644 title "Resistance management strategies in malaria vector mosquito control. A large-scale field trial in Southern Mexico" @default.
• W2133661644 cites W183141395 @default.
• W2133661644 cites W1984823070 @default.
• W2133661644 cites W1996998035 @default.
• W2133661644 cites W2014124488 @default.
• W2133661644 cites W2030904136 @default.
• W2133661644 cites W2040751216 @default.
• W2133661644 cites W2053640235 @default.
• W2133661644 cites W2055958238 @default.
• W2133661644 cites W2069412798 @default.
• W2133661644 cites W2075440229 @default.
• W2133661644 cites W2080103949 @default.
• W2133661644 cites W2123771845 @default.
• W2133661644 cites W2125447850 @default.
• W2133661644 cites W2171114940 @default.
• W2133661644 cites W2172278995 @default.
• W2133661644 cites W2311436108 @default.
• W2133661644 cites W2330055466 @default.
• W2133661644 cites W2332985104 @default.
• W2133661644 cites W2613741674 @default.
• W2133661644 doi "https://doi.org/10.1002/(sici)1096-9063(199711)51:3<375::aid-ps636>3.0.co;2-k" @default.
• W2133661644 hasPublicationYear "1997" @default.
• W2133661644 type Work @default.
• W2133661644 sameAs 2133661644 @default.
• W2133661644 citedByCount "54" @default.
• W2133661644 countsByYear W21336616442012 @default.
• W2133661644 countsByYear W21336616442013 @default.
• W2133661644 countsByYear W21336616442014 @default.
• W2133661644 countsByYear W21336616442015 @default.
• W2133661644 countsByYear W21336616442016 @default.
• W2133661644 countsByYear W21336616442017 @default.
• W2133661644 countsByYear W21336616442018 @default.
• W2133661644 countsByYear W21336616442019 @default.
• W2133661644 countsByYear W21336616442020 @default.
• W2133661644 countsByYear W21336616442022 @default.
• W2133661644 countsByYear W21336616442023 @default.
• W2133661644 crossrefType "journal-article" @default.
• W2133661644 hasAuthorship W2133661644A5017078169 @default.
• W2133661644 hasAuthorship W2133661644A5028559891 @default.
• W2133661644 hasAuthorship W2133661644A5041783872 @default.
• W2133661644 hasAuthorship W2133661644A5044985417 @default.
• W2133661644 hasAuthorship W2133661644A5067322954 @default.
• W2133661644 hasAuthorship W2133661644A5078298627 @default.
• W2133661644 hasAuthorship W2133661644A5083150936 @default.
• W2133661644 hasConcept C104317684 @default.
• W2133661644 hasConcept C104488531 @default.
• W2133661644 hasConcept C161176658 @default.
• W2133661644 hasConcept C181199279 @default.
• W2133661644 hasConcept C18903297 @default.
• W2133661644 hasConcept C203014093 @default.
• W2133661644 hasConcept C2776035571 @default.
• W2133661644 hasConcept C2776120307 @default.
• W2133661644 hasConcept C2776638905 @default.
• W2133661644 hasConcept C2776907368 @default.
• W2133661644 hasConcept C2778048844 @default.
• W2133661644 hasConcept C2778371730 @default.
• W2133661644 hasConcept C2778693464 @default.
• W2133661644 hasConcept C2779303437 @default.
• W2133661644 hasConcept C2779798688 @default.
• W2133661644 hasConcept C2780346216 @default.
• W2133661644 hasConcept C2781375639 @default.
• W2133661644 hasConcept C2908647359 @default.
• W2133661644 hasConcept C33070731 @default.
• W2133661644 hasConcept C40767141 @default.
• W2133661644 hasConcept C42972112 @default.
• W2133661644 hasConcept C538909803 @default.
• W2133661644 hasConcept C54355233 @default.
• W2133661644 hasConcept C55493867 @default.
• W2133661644 hasConcept C71924100 @default.
• W2133661644 hasConcept C86803240 @default.
• W2133661644 hasConcept C92087593 @default.
• W2133661644 hasConcept C99454951 @default.
• W2133661644 hasConceptScore W2133661644C104317684 @default.
• W2133661644 hasConceptScore W2133661644C104488531 @default.
• W2133661644 hasConceptScore W2133661644C161176658 @default.
• W2133661644 hasConceptScore W2133661644C181199279 @default.
• W2133661644 hasConceptScore W2133661644C18903297 @default.
• W2133661644 hasConceptScore W2133661644C203014093 @default.
• W2133661644 hasConceptScore W2133661644C2776035571 @default.
• W2133661644 hasConceptScore W2133661644C2776120307 @default.
• W2133661644 hasConceptScore W2133661644C2776638905 @default.
• W2133661644 hasConceptScore W2133661644C2776907368 @default.
• W2133661644 hasConceptScore W2133661644C2778048844 @default.
• W2133661644 hasConceptScore W2133661644C2778371730 @default.
• W2133661644 hasConceptScore W2133661644C2778693464 @default.
• W2133661644 hasConceptScore W2133661644C2779303437 @default.
• W2133661644 hasConceptScore W2133661644C2779798688 @default.

• next