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Margaret C. Wirth

Researcher at University of California, Riverside

Publications -  43
Citations -  1974

Margaret C. Wirth is an academic researcher from University of California, Riverside. The author has contributed to research in topics: Bacillus thuringiensis & Culex quinquefasciatus. The author has an hindex of 27, co-authored 43 publications receiving 1906 citations. Previous affiliations of Margaret C. Wirth include University of California.

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CytA enables CryIV endotoxins of Bacillus thuringiensis to overcome high levels of CryIV resistance in the mosquito, Culex quinquefasciatus

TL;DR: It is shown that high levels of resistance to CryIV proteins in larvae of the mosquito, Culex quinquefasciatus, can be suppressed or reduced markedly by combining these proteins with sublethal quantities of CytA, a cytolytic endotoxin of B. thuringiensis.
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Recombinant bacteria for mosquito control

TL;DR: The availability of these novel strains and newly discovered mosquitocidal proteins, such as the Mtx toxins of B. sphaericus, offers the potential for constructing a range of recombinant bacterial insecticides for more effective control of the mosquito vectors of filariasis, Dengue fever and malaria.
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Cyt1A of Bacillus thuringiensis delays evolution of resistance to Cry11A in the mosquito Culex quinquefasciatus.

TL;DR: Results indicate that Cyt1Aa is the principal factor responsible for delaying the evolution and expression of resistance to mosquitocidal Cry proteins.
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Potential for organophosphate resistance in Aedes aegypti (Diptera: Culicidae) in the Caribbean area and neighboring countries.

TL;DR: Populations of Aedes aegypti (L.) from 28 sites in Caribbean islands and neighboring countries were tested during 1983-85 for larval resistance to temephos, malathion, fenthion, and propoxur.
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Selection and characterization of temephos resistance in a population of Aedes aegypti from Tortola, British Virgin Islands.

TL;DR: Mendelian crosses indicated that temephos resistance was inherited as a monofactorial trait and the presence of elevated esterase activity was confirmed by biochemical tests; however, no evidence was found of insensitive acetylcholinesterase.