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1 o a heat spike in the larvae of the mosquito Culex pipiens.
2 ring adult ileum development in the mosquito Culex pipiens.
3 osquitoes, being shared by Aedes aegypti and Culex pipiens.
4 ference in the polymorphic mosquito species, Culex pipiens.
5 female A. albopictus, Anopheles sinensis and Culex pipiens.
6 n into cycle in the Northern house mosquito, Culex pipiens.
8 h detected high species diversity, including Culex pipiens, Aedes albopictus, Culex modestus, Anophel
9 We then performed competition assays between Culex pipiens and Aedes albopictus in low nutrient envir
10 le virus (WNV), previously was isolated from Culex pipiens and Aedes rossicus mosquitoes in the Czech
11 was isolated from two species of mosquitoes, Culex pipiens and Aedes vexans, and from brain tissues o
12 after blood feeding in two other mosquitoes (Culex pipiens and Anopheles gambiae) and the bed bug, Ci
14 ctipennis, and Anopheles punctulatus groups; Culex pipiens and the Culex subgenus Melanoconion; and t
15 fied between surface-dwelling populations of Culex pipiens and the so-called molestus form found in t
18 opictus and a representative native mosquito Culex pipiens by three native and widespread cyclopoid c
20 of the vector mosquitoes Aedes aegypti, the Culex pipiens Complex, and, most recently, Aedes albopic
21 ruses, including WNV, Culex tarsalis and the Culex pipiens complex, increased 17-21-fold with irrigat
22 n of 10 vector-pathogen pairs of mosquitoes (Culex pipiens, Cx. quinquefascsiatus, Cx. tarsalis, and
25 The populations of an aquatic invertebrate (Culex pipiens) exposed over several generations to repea
27 a widely cited example of urban adaptation, Culex pipiens form molestus, also known as the London Un
28 was vertically transmitted to 2 F(1) female Culex pipiens from a naturally infected female collected
30 cDNA from a WN virus isolate recovered from Culex pipiens in Connecticut was expressed in Escherichi
31 ticide resistance gene Ester in the mosquito Culex pipiens in the Montpellier area, southern France.
32 rmone signaling direct entry of the mosquito Culex pipiens into its overwintering adult diapause, and
35 intering dormancy (diapause) in the mosquito Culex pipiens is the switch in females from blood feedin
37 this hypothesis using different incompatible Culex pipiens mosquito strains and show that CI persists
38 he function of sfRNA during WNV infection of Culex pipiens mosquitoes and evaluated its role in deter
40 nyavirus close to Umbre virus, were found in Culex pipiens mosquitoes captured in the south of France
41 l-sib design was set up in which families of Culex pipiens mosquitoes collected from the field were r
42 HCR), a phenotype first described in 1999 in Culex pipiens mosquitoes surviving chlorpyrifos doses 1
44 lly tested using larval Aedes albopictus and Culex pipiens mosquitoes to assess mortality and percent
50 sly associated with pyrethroid resistance in Culex pipiens pallens was also over-transcribed in VK.
51 of mosGCTL in another major mosquito vector (Culex pipiens pallens) also impairs the survival of gut
53 y receptor neurons (ORNs) on the antennae of Culex pipiens quinquefasciatus (Cx. quinquefasciatus).
56 LPs to address biological questions in vivo, Culex pipiens quinquefasciatus mosquitoes were orally an
57 tected USUV RNA in host-seeking adult female Culex pipiens s.l. as well as in adults reared from fiel
60 . quinquefasciatus is one species within the Culex pipiens species complex and can be found throughou
61 bachia strains circulating in the California Culex pipiens species complex, (2) investigate Wolbachia
62 lengths of late summer program the mosquito Culex pipiens to enter a reproductive diapause character