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 cally relevant range for humans and infected Aedes aegypti.

3 on the behavior of the yellow fever mosquito Aedes aegypti.

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

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

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

7 homeostasis and dengue virus replication in Aedes aegypti.

8 es from the mosquitoes Anopheles gambiae and Aedes aegypti.

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

10 for DENV and YFV than an urban population of Aedes aegypti.

11 eles stephensi and the yellow fever mosquito Aedes aegypti.

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

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

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

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

16 feeding and egg development in the mosquito Aedes aegypti.

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

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

19 ivergent relative, the yellow fever mosquito Aedes aegypti.

20 2 cDNA clone from the yellow fever mosquito, Aedes aegypti.

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

22 in some important mosquito vectors, notably Aedes aegypti.

23 We address this gap in the arboviral vector Aedes aegypti.

24 d the role of actin bundles in the mosquito, Aedes aegypti.

25 milar manner to that previously described in Aedes aegypti.

26 between tethered female and free-flying male Aedes aegypti.

27 pond sensitively to a variety of odorants in Aedes aegypti.

28 populations of the primary vector mosquito, Aedes aegypti.

29 e transmitted by the disease vector mosquito Aedes aegypti.

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

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

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

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

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

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

36 e a comprehensive picture of the lipidome of Aedes aegypti (Aag2) cells infected with Wolbachia only,

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

38 hree widely distributed species of mosquito; Aedes aegypti, Ae. albopictus and Culex quinquefasciatus

39 We observed that gravid Aedes aegypti, Ae. albopictus, and Culex quinquefasciatu

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

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

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

43 otion, pose, biting, and feeding dynamics of Aedes aegypti, Aedes albopictus, Anopheles stephensi, an

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

45 ition to its important role in protection of Aedes aegypti against heme exposure, also acts as a dige

46 -activator odorants identified originally in Aedes aegypti also showed varying ability to reduce the

47 The yellow fever mosquito Aedes aegypti, an important vector of human infectious d

48 mechanistic phenology model and apply it to Aedes aegypti, an invasive mosquito vector for arbovirus

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

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

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

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

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

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

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

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

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

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

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

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

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

62 l DENV transmission by the mosquito vectors, Aedes aegypti and Aedes albopictus, using the Wolbachia

63 nges in the distribution of two key vectors: Aedes aegypti and Aedes albopictus.

64 Aedes aegypti and Anopheles coluzzii mosquitoes exhibit

65 Aedes aegypti and Anopheles gambiae harbor the causative

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

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

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

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

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

73 Aedes aegypti and Culex quinquefasciatus were found year

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 unya viruses are transmitted by the mosquito Aedes aegypti and pose a substantial threat to global pu

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

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

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

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

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

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

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

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

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

89 Anopheles gambiae and Aedes aegypti are perhaps the best studied mosquito spec

90 e show that Aedes spp. mosquitoes, including Aedes aegypti, are effective pollinators of the Platanth

91 ize that mosquito vector species, especially Aedes aegypti, are locally concentrated primarily in tho

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 Identifying Aedes aegypti breeding hotspots in urban areas is crucia

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

100 nificantly shortens the EIP of ZIKV-infected Aedes aegypti by enhancing virus dissemination from the

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

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

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

104 quito larvae and pupae, including from field Aedes aegypti can acquire ZIKV from contaminated aquatic

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

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

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

108 The range of the mosquito Aedes aegypti continues to expand, putting more than two

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

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

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

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

113 RNAi suppressor B2 from Flock House virus or Aedes aegypti dicer-2 (Aedicer-2) using a constitutive h

114 ancudomyces culisetae) in a larval mosquito (Aedes aegypti) digestive tract affected microbiomes in l

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

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

117 Aedes aegypti egg survival was unaffected by exposure to

118 ing ZIKV is expressed and fully processed in Aedes aegypti, ensuring the formation of mature syntheti

119 ntal data on the effects of transfluthrin on Aedes aegypti explores how SR effects interact to impact

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

121 Aedes aegypti females must accurately discriminate blood

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

123 Aedes aegypti females typically mate once, requiring the

124 In Aedes aegypti females, the ammonia released during blood

125 te the impacts of Brugia malayi infection on Aedes aegypti flight parameters: distance, average speed

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

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

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

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

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

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

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

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

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

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

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

137 Here we show that the Aedes aegypti heme oxygenase gene (AeHO - AAEL008136) is

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

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

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

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

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

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

144 quitoes Anopheles gambiae, An. coluzzii, and Aedes aegypti in which we determine that ~90% of all pro

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

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

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

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

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

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

151 The mosquito Aedes aegypti is a major arbovirus vector native to Afri

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

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

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

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

156 Aedes aegypti is the main vector of arboviral diseases s

157 Aedes aegypti is the main vector of dengue, Zika, chikun

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

159 Aedes aegypti is the most synanthropic and anthropophili

160 Aedes aegypti is the primary vector for transmission of

161 Aedes aegypti is the primary vector of a number of virus

162 Aedes aegypti is the principal mosquito vector for many

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

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

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

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

167 Aedes aegypti kynurenine aminotransferase (AeKAT) is a m

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

169 body and epidermis of yellow fever mosquito, Aedes aegypti larvae.

170 ction with different membranes, including in Aedes aegypti larval brush border membrane vesicles, sma

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

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

173 Aedes aegypti manipulated genetically to express gene-sp

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

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

176 This study sought to gain insights into how Aedes aegypti midgut microbes and life history traits ar

177 Aedes aegypti mosGCTLs facilitate colonization by multip

178 owed by exposure to feeding by an uninfected Aedes aegypti mosquito at day 42 to assess subsequent ri

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

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

181 mpaired arboviral infection of a lab-adapted Aedes aegypti mosquito strain.

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

183 The Aedes aegypti mosquito transmits arboviruses, including

184 s of 8506 hemocytes of Anopheles gambiae and Aedes aegypti mosquito vectors.

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

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

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

188 ging flavivirus primarily transmitted by the Aedes aegypti mosquito, we screened for antigenic SG pro

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

190 orne flavivirus predominantly transmitted by Aedes aegypti mosquitoes and poses a global human health

191 Female Aedes aegypti mosquitoes are deadly vectors of arboviral

192 Aedes aegypti mosquitoes are important vectors of viral

193 Aedes aegypti mosquitoes are responsible for transmittin

194 previously observed that orco mutant female Aedes aegypti mosquitoes are strongly attracted to human

195 Aedes aegypti mosquitoes are the primary vectors of nume

196 Female Aedes aegypti mosquitoes bite humans to obtain blood to

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

198 Aedes aegypti mosquitoes carrying a conditionally lethal

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

200 fevers, a strain of transgenically modified Aedes aegypti mosquitoes containing a dominant lethal ge

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

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

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

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

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

206 Mating behavior in Aedes aegypti mosquitoes occurs mid-air and involves the

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

208 Female Aedes aegypti mosquitoes require protein from blood to d

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

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

211 a virus is predominantly mosquito-borne, and Aedes aegypti mosquitoes serve as a key vector for Zika

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

213 ere evaluated as mosquito repellents against Aedes aegypti mosquitoes that transmit the Zika and Deng

214 s experimental study we film the landings of Aedes aegypti mosquitoes to characterize landing behavio

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

216 Biocontrol programs are underway using Aedes aegypti mosquitoes trans-infected with a non-natur

217 Aedes aegypti mosquitoes transmit pathogens such as yell

218 and dissemination rates were not different, Aedes aegypti mosquitoes transmitted ZIKV I1404 more poo

219 Female Aedes aegypti mosquitoes typically mate only once with o

220 Female Aedes aegypti mosquitoes use multiple sensory modalities

221 Aedes aegypti mosquitoes vector several arboviruses of g

222 that we discovered in a laboratory colony of Aedes aegypti mosquitoes was similarly efficient.

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

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

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

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

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

228 with a closely related partitivirus found in Aedes aegypti mosquitoes, is transmitted from infected f

229 between outbreaks of viruses transmitted by Aedes aegypti mosquitoes, such as chikungunya, dengue, a

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

231 previously reported the generation of axenic Aedes aegypti mosquitoes, the primary vector of several

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

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

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

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

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

237 ich are all caused by viruses transmitted by Aedes aegypti mosquitoes.

238 3 and -4, which are transmitted to people by Aedes aegypti mosquitoes.

239 f the intracellular bacterium Wolbachia into Aedes aegypti mosquitoes.

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

241 survival, fecundity, and metabolism of adult Aedes aegypti mosquitoes.

242 ting double-stranded RNA (dsRNA) into female Aedes aegypti mosquitoes.

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

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

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

246 The NTD-core domain of Aedes aegypti Nbr adopts a HEAT-like repeat scaffold wit

247 male sex (M/m) in the yellow fever mosquito, Aedes aegypti Nix, a gene in the M-locus, was shown to b

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

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

250 usly, the functional ablation of a family of Aedes aegypti olfactory receptors, the odorant receptors

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

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

253 Day-biting mosquitoes Aedes aegypti, particularly females, are attracted to li

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

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

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

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

258 show that a satellite repeat in the mosquito Aedes aegypti promotes sequence-specific gene silencing

259 ive organs of the arboviral vector mosquito, Aedes aegypti, prompting us to explore the role of AMTs

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

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

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

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

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

265 We found that a strain of Aedes aegypti that is refractory to infection by Dirofil

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

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

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

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

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

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

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

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

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

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

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

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

278 and the globally important mosquito species, Aedes aegypti, through a combination of live mosquito ex

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

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

281 Aedes aegypti transmit pathogenic arboviruses while the

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

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

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

285 e find that a saliva-specific protein, named Aedes aegypti venom allergen-1 (AaVA-1), promotes dengue

286 Dengue virus acquisition by Aedes aegypti was inversely correlated with the iron con

287 Aedes aegypti was negatively affected by interspecific c

288 Aedes aegypti was primarily found in buckets, bromeliads

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

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

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

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

293 he first time to study sperm of the mosquito Aedes aegypti, we reveal that sperm shed their entire ou

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

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

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

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

298 Primary transmission usually involves Aedes aegypti, which has expanded its distribution range

299 hroids are the main adulticides used against Aedes aegypti, which vectors pathogens such as Zika viru

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