ライフサイエンスコーパス: Aedes aegypti

1 ea squirt (Ciona savignyi) and the mosquito (Aedes aegypti).

2 e transmitted by the disease vector mosquito Aedes aegypti.

3 t maintenance in the dengue mosquito vector, Aedes aegypti.

4 n (PE) development in the fat body of female Aedes aegypti.

5 feeding and egg development in the mosquito Aedes aegypti.

6 f fruit flies and the yellow fever mosquito, Aedes aegypti.

7 pora allata-corpora cardiaca of the mosquito Aedes aegypti.

8 cally relevant range for humans and infected Aedes aegypti.

9 ivergent relative, the yellow fever mosquito Aedes aegypti.

10 2 cDNA clone from the yellow fever mosquito, Aedes aegypti.

11 ation of Toll immune pathway in the mosquito Aedes aegypti.

12 in some important mosquito vectors, notably Aedes aegypti.

13 was discovered in the yellow fever mosquito, Aedes aegypti.

14 ene from transgenic yellow fever mosquitoes, Aedes aegypti.

15 ogous to Drosophila Relish from the mosquito Aedes aegypti.

16 n biosynthesis in the yellow fever mosquito, Aedes aegypti.

17 ant than MITEs in the yellow fever mosquito, Aedes aegypti.

18 imilar kinetics as seen in the mosquito host Aedes aegypti.

19 th distinct N-termini, occur in the mosquito Aedes aegypti.

20 alivary glands of the yellow fever mosquito, Aedes aegypti.

21 m the hemolymph of bacteria-challenged adult Aedes aegypti.

22 anticoagulant of the yellow fever mosquito, Aedes aegypti.

23 e to the biology and behavior of its vector, Aedes aegypti.

24 embryonic soma of the yellow fever mosquito, Aedes aegypti.

25 his mosquito species using RFLP markers from Aedes aegypti.

26 are described in the yellow fever mosquito, Aedes aegypti.

27 isolated from a cDNA library of the mosquito Aedes aegypti.

28 emale fat body cDNA library of the mosquito, Aedes aegypti.

29 Habrobracon) hebetor and a diploid mosquito. Aedes aegypti.

30 micro-injection into embryos of the mosquito Aedes aegypti.

31 quefasciatus, and the yellow fever mosquito, Aedes aegypti.

32 y arthropods, generally, using the mosquito, Aedes aegypti.

33 homeostasis and dengue virus replication in Aedes aegypti.

34 E-binding proteins from the mosquito species Aedes aegypti.

35 es from the mosquitoes Anopheles gambiae and Aedes aegypti.

36 alanine aminotransferase (ALAT) in blood-fed Aedes aegypti.

37 eles stephensi and the yellow fever mosquito Aedes aegypti.

38 he male and female germline, in the mosquito Aedes aegypti.

39 of spermatozoa in the yellow fever mosquito, Aedes aegypti.

40 antennal lobe of the yellow fever mosquito, Aedes aegypti, a major vector of arboviral diseases.

41 the impact of transgenesis on the fitness of Aedes aegypti, a mosquito that transmits yellow fever.

42 smodium protozoan agent causing malaria, and Aedes aegypti, a vector for the flaviviral agents causin

43 splicing in Manduca sexta, Bombyx mori, and Aedes aegypti: A C-terminally amidated ITP and a C-termi

44 uence of the yellow fever and Dengue vector, Aedes aegypti (Aa), has enabled a comparative phylogenom

45 We show that Aedes aegypti Aag2 cells - an immune responsive cell lin

46 thione S-transferase (GST) from the mosquito Aedes aegypti (aagste2), selected in the field as a majo

47 midgut of the Yellow Fever vector mosquito, Aedes aegypti (aeAAT1, AAR08269), which primarily suppli

48 l crystal structure of AGT from the mosquito Aedes aegypti (AeAGT) and structures of its complexes wi

49 omain D7 proteins from Anopheles gambiae and Aedes aegypti (AeD7), respectively, were shown to bind b

50 loned from the renal (Malpighian) tubules of Aedes aegypti (AeKir1).

51 in immunity by generating a total of 11,952 Aedes aegypti and 12,790 Armigeres subalbatus expressed

52 tein-coding genes is 22% larger than that of Aedes aegypti and 52% larger than that of Anopheles gamb

53 d-borne viruses, is transmitted to humans by Aedes aegypti and A. albopictus mosquitoes in tropical a

54 ype 1 [DENV-1] to DENV-4) are transmitted by Aedes aegypti and A. albopictus mosquitoes, causing up t

55 -emerging arbovirus transmitted to humans by Aedes aegypti and Ae. albopictus mosquitoes, causes debi

56 gaviridae, which is transmitted to humans by Aedes aegypti and Ae. albopictus.

57 smitted among humans by the mosquito vectors Aedes aegypti and Aedes albopictus are hypothesized to h

58 nya virus (CHIKV) is primarily spread by the Aedes aegypti and Aedes albopictus mosquito vectors.

59 Chikungunya virus (CHIKV) is transmitted by Aedes aegypti and Aedes albopictus mosquitoes and causes

60 virus (DENV1-DENV4) are spread primarily by Aedes aegypti and Aedes albopictus mosquitoes, whose geo

61 IKV) is a reemerging pathogen transmitted by Aedes aegypti and Aedes albopictus mosquitoes.

62 porary distribution of their shared vectors, Aedes aegypti and Aedes albopictus remains incomplete an

63 ly includes two key mosquito vector species: Aedes aegypti and Aedes albopictus The model was paramet

64 , we highlight biological characteristics of Aedes aegypti and Aedes albopictus, 2 invasive mosquito

65 s, include the release of Wolbachia-infected Aedes aegypti and Aedes albopictus, for either its virus

66 hat is secreted from cells derived from both Aedes aegypti and Aedes albopictus.

67 A unique feature of the R7 photoreceptors in Aedes aegypti and Anopheles gambiae is the extreme apica

68 For example, ITmD37E sequences from Aedes aegypti and Anopheles gambiae, which have an estim

69 tive detector of human skin odorants in both Aedes aegypti and Anopheles gambiae.

70 mmune gene repertoire compared with those of Aedes aegypti and Anopheles gambiae.

71 re insecticidal to larvae of the mosquitoes, Aedes aegypti and Anopheles gambiae.

72 ediculus humanus humanus, Anopheles gambiae, Aedes Aegypti and Culex pipiens quinquefasciatus is nota

73 s ancient within mosquitoes, being shared by Aedes aegypti and Culex pipiens.

74 mosquitoes (three Anopheles gambiae genomes, Aedes aegypti and Culex quinquefasciatus), tick (Ixodes

75 , in two closely related species of insects: Aedes aegypti and Culex quinquefasciatus.

76 We use Aedes aegypti and dengue virus (DENV) for illustrative p

77 o maintaining homeostasis in the gut of both Aedes aegypti and Drosophila melanogaster.

78 Discovery of the Muta1 element from Aedes aegypti and its successful transposition in yeast

79 s assumption using the yellow fever mosquito Aedes aegypti and malaria parasite Plasmodium gallinaceu

80 reduced the infectivity of P. gallinaceum to Aedes aegypti and P. falciparum to Anopheles mosquitoes.

81 p and physiology of aaNATs from the mosquito Aedes aegypti and serve as a reference for studying the

82 or Anopheles gambiae and a D7 long form from Aedes aegypti and showed by isothermal microcalorimetry,

83 AT transposons, AeBuster1, from the mosquito Aedes aegypti and TcBuster from the red flour beetle Tri

84 tionally, recombinant ZIKV is infectious for Aedes aegypti and thus provides a means to examine virus

85 er accession numbers AY 431103 to AY 433788 (Aedes aegypti) and AY 439334 to AY 441440 (Armigeres sub

86 om two other insects (Drosophila virilis and Aedes aegypti) and three vertebrates (Homo sapiens, Mus

87 ms such as Bombyx mori, Tribolium casteneum, Aedes aegypti, and Anopheles stephensi.

88 quences are available for Anopheles gambiae, Aedes aegypti, and Culex quinquefasciatus.

89 nt region has expanded in Anopheles gambiae, Aedes aegypti, and Tribolium castaneum, while the PF rep

90 nome information for three mosquito species: Aedes aegypti, Anopheles gambiae and Culex quinquefascia

91 e sequence data are available for 3 species, Aedes aegypti, Anopheles gambiae, and Culex quinquefasci

92 Aedes albopictus is secondary to Aedes aegypti as a vector of dengue viruses (DENVs) in s

93 idemic spread widely to many countries where Aedes Aegypti as the main transmitting vector is endemic

94 age-specific and density dependent change in Aedes aegypti behaviour towards host cues when exposed t

95 Aegyptin, a secreted salivary protein from Aedes aegypti, binds collagen and inhibits platelet aggr

96 viduals may become infected by more than one Aedes aegypti-borne virus at a time.

97 In the yellow fever and dengue vector Aedes aegypti, both sexes interact acoustically by shift

98 uced local populations of the dengue vector, Aedes aegypti, but challenges remain in scale and in sep

99 otein inhibits RNA silencing in the mosquito Aedes aegypti by interfering with Dicer.

100 enin (Vg) gene in the yellow fever mosquito, Aedes aegypti, by EcR/USP and E74 in response to an elev

101 We now show that an Aedes aegypti C-type lectin, mosGCTL-1, is induced by WN

102 A recent Aedes aegypti case study demonstrates the viability of o

103 fitness of two clades of DENV serotype 2 in Aedes aegypti cells and mosquitoes collected from the re

104 Aedes aegypti chorion peroxidase (CPO) plays a crucial r

105 including DENV and Zika virus transmitted by Aedes aegypti, continue to be a threat to global health

106 Overexpressing wild-type AeSCP-2 in the Aedes aegypti cultured Aag-2 cells resulted in an increa

107 Aedes aegypti densonucleosis virus (AeDNV) has two promo

108 Sequencing of small RNAs from KC and Aedes aegypti-derived Aag2 cells infected with BTV or th

109 e nuclear factor-4 (HNF-4) from the mosquito Aedes aegypti, designated AaHNF-4a, AaHNF-4b, and AaHNF-

110 imensional solution structures of SCP-2 from Aedes aegypti determined by NMR spectroscopy in its liga

111 occurred in 95-100% of the larval cohorts of Aedes aegypti developing at those sites.

112 ted that several mosquito species, including Aedes aegypti, do not develop beyond the first instar wh

113 ets, S6 kinase, of the yellow fever mosquito Aedes aegypti during egg development in adult females.

114 Aedes aegypti egg survival was unaffected by exposure to

115 The mosquito Aedes aegypti expresses the long-wavelength rhodopsin Aa

116 Newly emerged Aedes aegypti females require 3 days before becoming com

117 In this study behavioral assays identified Aedes aegypti females that were insensitive to DEET, and

118 In Aedes aegypti females, the ammonia released during blood

119 prefers a specific cell type (Ross cell) in Aedes aegypti for crossing the midgut epithelium.

120 tory region of the vitellogenin (Vg) gene of Aedes aegypti for its ability to express potential antip

121 We tested female yellow fever mosquitoes (Aedes aegypti) for responses to 8-hydroxy-8-methyl-6-(2'

122 The yellow fever mosquito Aedes aegypti forms aerial swarms that serve as mating a

123 Two approaches were used to correlate the Aedes aegypti genetic linkage map to the physical map.

124 h DENV serotype 2 strain 1232 at sites where Aedes aegypti had or had not probed immediately prior.

125 host and, when introduced into the mosquito Aedes aegypti, halves its life span.

126 le as the primary vector for dengue viruses, Aedes aegypti has a long history as a genetic model orga

127 The yellow fever mosquito Aedes aegypti has been the subject of extensive genetic

128 A 'domestic' form of the mosquito Aedes aegypti has evolved to specialize in biting humans

129 omorphic sex chromosomes, while the mosquito Aedes aegypti has homomorphic sex chromosomes.

130 The mosquito Aedes aegypti has ten PPO genes in the genome, four of w

131 Anopheles gambiae and Aedes aegypti have evolved a strong preference for human

132 ciatus, and Cx. pipiens) and bridge vectors (Aedes aegypti) have differential impacts on viral mutati

133 eloped for the major mosquito disease vector Aedes aegypti Here, we describe the generation of multip

134 S1 was successfully detected in spiked adult Aedes aegypti homogenate over a broad dynamic range with

135 s in JH responsive Aag-2 cells revealed that Aedes aegypti homologues of both Met and SRC are require

136 ciphered how Wolbachia infection affects the Aedes aegypti host in inducing resistance to DENV.

137 rs of human pathogens (Anopheles gambiae and Aedes aegypti) imbibing multiple bloodmeals during a gon

138 amine the breeding structure of the mosquito Aedes aegypti in Puerto Rico.

139 nt populations of the yellow fever mosquito, Aedes aegypti in the southeastern United States and in B

140 pression of a sodium channel, AaNav1-1, from Aedes aegypti in Xenopus oocytes, and the functional exa

141 ards the vertebrate host and, in the case of Aedes aegypti, increased sensitivity to skin odours.

142 rior studies with the yellow fever mosquito, Aedes aegypti, indicated blood feeding stimulates egg pr

143 terfering RNAs (viRNAs), 21 nt in length, in Aedes aegypti infected with the mosquito-borne virus, Si

144 The gene Aedes aegypti intestinal mucin 1 (AeIMUC1) encodes a put

145 gal-specific immune response in the mosquito Aedes aegypti involves the Toll immune pathway transduce

146 The mosquito Aedes aegypti is a major vector of numerous viral diseas

147 Sex determination in the mosquito Aedes aegypti is governed by a dominant male-determining

148 Before blood feeding, Aedes aegypti is in a state of reproductive arrest durin

149 The mosquito Aedes aegypti is more widely dispersed now than at any t

150 The mosquito Aedes aegypti is one of the most important disease vecto

151 The mosquito Aedes aegypti is the major vector of arboviral diseases,

152 The mosquito Aedes aegypti is the most important vector of yellow fev

153 The mosquito Aedes aegypti is the principal vector for the yellow fev

154 The mosquito Aedes aegypti is the principal vector of dengue and yell

155 The mosquito Aedes aegypti is the world's most important vector of ye

156 quitoes of the major vector of Dengue fever, Aedes aegypti, is cyclic because of its dependence on bl

157 an YF, owing to transmission of the virus by Aedes aegypti, is increasing in Africa, as is the potent

158 Aedes aegypti kynurenine aminotransferase (AeKAT) is a m

159 In females of the mosquito vector Aedes aegypti (L.), aedeskinins are known to stimulate f

160 are used for host location by the mosquito, Aedes aegypti (L.).

161 The enzyme was purified from Aedes aegypti larvae by ammonium sulfate fractionation,

162 of movement of the primary mosquito vector, Aedes aegypti, local human movements may be an important

163 rculates in the hemolymph of pupal and adult Aedes aegypti males and females.

164 Aedes aegypti manipulated genetically to express gene-sp

165 on hosts and peridomestic mosquitoes, mainly Aedes aegypti, mediate human-to-human transmission.

166 irus (SINV) strain MRE16 efficiently infects Aedes aegypti midgut epithelial cells (MEC), but laborat

167 parum, selectively invade a cell type in the Aedes aegypti midgut.

168 Aedes aegypti mosGCTLs facilitate colonization by multip

169 uantification of the effects of Wolbachia in Aedes aegypti mosquito cells and midgut.

170 ragment length polymorphisms of four natural Aedes aegypti mosquito populations from Trinidad and Tob

171 We show here that the Aedes aegypti mosquito possesses two distinct light-driv

172 in displays sequence identities of 70% to an Aedes aegypti mosquito TA receptor, followed by 60% to a

173 The Aedes aegypti mosquito transmits arboviruses, including

174 The Zika outbreak, spread by the Aedes aegypti mosquito, highlights the need to create hi

175 V) is primarily transmitted to humans by the Aedes aegypti mosquito, human-to-human transmission has

176 us-Zika virus-spread by the same vector, the Aedes aegypti mosquito, that also carries dengue, yellow

177 Dengue virus infection in Aedes aegypti mosquitoes activates the JAK-STAT immune s

178 eudoobscura, and homologs have been found in Aedes aegypti mosquitoes and in four other insect orders

179 Aedes aegypti mosquitoes are important vectors of viral

180 Aedes aegypti mosquitoes are responsible for transmittin

181 ntitrypsin antibodies blocked infectivity of Aedes aegypti mosquitoes by Plasmodium gallinaceum.

182 n in mosquitoes, we manipulated apoptosis in Aedes aegypti mosquitoes by silencing the expression of

183 Aedes aegypti mosquitoes carrying a conditionally lethal

184 nitiated infection and transmission rates in Aedes aegypti mosquitoes comparable to those of the prim

185 n from symptomatic dengue cases (n = 208) to Aedes aegypti mosquitoes during 407 independent exposure

186 f the endosymbiotic bacterium Wolbachia into Aedes aegypti mosquitoes has the potential to greatly re

187 Chikungunya virus is mainly transmitted by Aedes aegypti mosquitoes in tropical and subtropical reg

188 WsnRNAs were detected in Aedes aegypti mosquitoes infected with the wMelPop-CLA s

189 Here, we show that in female Aedes aegypti mosquitoes JH III control of gene expressi

190 Xanthine dehydrogenase-1 silencing in Aedes aegypti mosquitoes promotes a blood feeding-induce

191 tive disposal of nitrogen waste in blood-fed Aedes aegypti mosquitoes requires alanine aminotransfera

192 ), Cecropin A, and Defensin A, in transgenic Aedes aegypti mosquitoes results in the cooperative anti

193 nate metabolic pathway for urea synthesis in Aedes aegypti mosquitoes that converts uric acid to urea

194 ogaviridae) strain MRE16 efficiently infects Aedes aegypti mosquitoes that ingest a blood meal contai

195 f Wolbachia can reduce the permissiveness of Aedes aegypti mosquitoes to disseminated arboviral infec

196 Female Aedes aegypti mosquitoes typically mate only once with o

197 Aedes aegypti mosquitoes vector several arboviruses of g

198 Field-collected and laboratory-colonized Aedes aegypti mosquitoes were fed on blood containing ea

199 ENV), deep sequencing data of virus-infected Aedes aegypti mosquitoes were used.

200 osis during arbovirus infection by infecting Aedes aegypti mosquitoes with a Sindbis virus (SINV) clo

201 say systems (using human dendritic cells and Aedes aegypti mosquitoes) for measuring differences in v

202 achia spreads rapidly through populations of Aedes aegypti mosquitoes, and strongly inhibits infectio

203 ication of dengue virus when introduced into Aedes aegypti mosquitoes, as well as to stimulate chroni

204 ilar rates of infection and dissemination in Aedes aegypti mosquitoes, suggesting differing roles for

205 these MAbs on P. gallinaceum infectivity for Aedes aegypti mosquitoes, the addition of MAbs 1A6 and 2

206 and DENV together in the saliva of infected Aedes aegypti mosquitoes, these findings suggest a mecha

207 However, in 2007, vectored by Aedes aegypti mosquitoes, ZIKV caused the first notewort

208 a subunit of the heteromeric CO2 receptor in Aedes aegypti mosquitoes.

209 cells, and for productive DENV infection of Aedes aegypti mosquitoes.

210 s carbon routes during ammonia metabolism of Aedes aegypti mosquitoes.

211 icate and produce disseminated infections in Aedes aegypti mosquitoes.

212 cing ZIKV genomes from infected patients and Aedes aegypti mosquitoes.

213 3 and -4, which are transmitted to people by Aedes aegypti mosquitoes.

214 f the intracellular bacterium Wolbachia into Aedes aegypti mosquitoes.

215 is required for DENV-2 replication in adult Aedes aegypti mosquitos implying that the requirement fo

216 opical disease that is transmitted by female Aedes Aegypti mosquitos.

217 EL1 (Gambif1) from the yellow fever mosquito Aedes aegypti, named AaREL1.

218 In the female mosquito, Aedes aegypti, neurohormones are released from the brain

219 epidemics presumably involve transmission by Aedes aegypti, no direct evidence of vector involvement

220 report on the characterization in transgenic Aedes aegypti of two mosquito gut-specific promoters.

221 Florida, the mosquitoes Aedes albopictus and Aedes aegypti often co-occur in water-filled containers

222 NV) are transmitted to humans by the bite of Aedes aegypti or Aedes albopictus mosquitoes, with milli

223 t hairpin RNAs (shRNAs) corresponding to the Aedes aegypti orthologs of fasciculation and elongation

224 The yellow fever mosquito, Aedes aegypti, particularly in Neotropical regions, is t

225 Aedes aegypti PISCF-allatostatin or allatostatin-C (Ae-A

226 hree different vector-parasite combinations, Aedes aegypti-Plasmodium gallinaceum, Anopheles stephens

227 el driven by meteorological data to simulate Aedes aegypti populations and dengue cases in 23 locatio

228 nctioned as a potent ligand for the mosquito Aedes aegypti receptor complex (AaEcR-USP), significantl

229 and 26-kDa ferritin subunits in the mosquito Aedes aegypti (Rockefeller strain).

230 Serine protease activity in Aedes aegypti saliva augmented virus infectivity in vitr

231 erkingdom cue for the yellow fever mosquito, Aedes aegypti, seeking blood-meals as well as ovipositio

232 The mosquito Aedes aegypti shows a robust response, losing nearly all

233 N(1575)Y + L(1014)F were introduced into an Aedes aegypti sodium channel, AaNav1-1, and the mutants

234 ss have previously been found to attract the Aedes aegypti species of mosquito.

235 ction and assignment results for the protein Aedes aegypti sterol carrier protein 2.

236 test this hypothesis, germ-line-transformed Aedes aegypti that express luciferase (LUC) from the mos

237 tion; particularly, for the 1.3 GB genome of Aedes aegypti the mean value of prediction Sensitivity a

238 In the mosquito Aedes aegypti, the adult female becomes competent for a

239 s gambiae and Anopheles coluzzii, as well as Aedes aegypti, the cosmopolitan vector of dengue, chikun

240 e waves of invasion of the vector mosquitoes Aedes aegypti, the Culex pipiens Complex, and, most rece

241 sion and that, in the yellow fever mosquito, Aedes aegypti, the expression of the ferritin heavy-chai

242 In the mosquito Aedes aegypti, the expression of two fat body genes invo

243 The yellow fever mosquito, Aedes aegypti, the global vector of dengue and yellow fe

244 opheles gambiae, Culex quinquefasciatus, and Aedes aegypti, the latter an important Zika and Dengue v

245 flavivirus that is primarily transmitted by Aedes aegypti, the mosquito vector also important in tra

246 We present a draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and d

247 Aedes aegypti, the primary vector of dengue virus, is we

248 In the mosquito Aedes aegypti, the sex-determining chromosomes are homom

249 -mediated cassette exchange (RMCE) system to Aedes aegypti, the vector of dengue, chikungunya, and Zi

250 We found that in the mosquito Aedes aegypti, there are two distinct melanization activ

251 Here we elucidate the basic rules of Aedes aegypti thermotaxis and test the function of candi

252 (QTL) affecting the ability of the mosquito Aedes aegypti to become infected with dengue-2 virus wer

253 COPI functions in the Yellow Fever mosquito Aedes aegypti to interfere with blood meal digestion.

254 thologous gene of the yellow fever mosquito, Aedes aegypti, to control sex- and tissue-specific expre

255 determining susceptibility of the mosquito, Aedes aegypti, to the malarial parasite, Plasmodium gall

256 Blood feeding by the vector mosquito Aedes aegypti triggers the release of two neurohormones,

257 Feeding of soybean trypsin inhibitor and Aedes aegypti trypsin modulating oostatic factor affecte

258 imfast (Slif) from the yellow-fever mosquito Aedes aegypti using codon-optimized heterologous express

259 An antiserum raised against recombinant Aedes aegypti V-ATPase B subunit indicated that the majo

260 ful completion of the infection cycle in the Aedes aegypti vector, which is initiated in the midgut t

261 aper, we analyzed the upstream region of the Aedes aegypti Vg gene in order to identify regulatory el

262 The mosquito (Aedes aegypti) vitellogenin receptor (AaVgR) is a large

263 Aedes aegypti was negatively affected by interspecific c

264 ve linkage map of the yellow fever mosquito, Aedes aegypti, was constructed using single-strand confo

265 ignated OX3604C, of the major dengue vector, Aedes aegypti, was engineered to have a repressible fema

266 By using the yellow fever mosquito, Aedes aegypti, we demonstrate that this boost in tempera

267 Using the mosquito Aedes aegypti, we determined that mutations in the FokI

268 tissue from larvae of the non-target insect Aedes aegypti, we isolated a number of phage for further

269 sed of large bacterial-type proteins that in Aedes aegypti were implicated as receptors for Plasmodiu

270 pheles gambiae and the yellow fever mosquito Aedes aegypti were searched by Blast against each Plus-C

271 Mosquitoes (Aedes aegypti) were genetically modified to exhibit impa

272 ransferred from Drosophila into the mosquito Aedes aegypti, where it can block the transmission of de

273 ines ZIKV infectivity in its mosquito vector Aedes aegypti, which acquires ZIKV via a blood meal.

274 oid X receptor homologue, from the mosquito, Aedes aegypti, which form a functional complex capable o

275 the family of 30-kDa salivary allergens from Aedes aegypti, whose function remained elusive thus far.

276 t Sindbis virus was used to transduce female Aedes aegypti with a 567-base antisense RNA targeted to

277 ional structure of the complex of SCP-2 from Aedes aegypti with a C16 fatty acid to 1.35-A resolution

278 ted immune deficiency (RMID) by transforming Aedes aegypti with the Delta Rel transgene driven by the