ライフサイエンスコーパス: Anopheles gambiae

1 f specific ORs of the African malaria vector Anopheles gambiae.

2 are involved in anti-Plasmodium responses in Anopheles gambiae.

3 pression system for the major malaria vector Anopheles gambiae.

4 uman skin odorants in both Aedes aegypti and Anopheles gambiae.

5 n the legs, confers pyrethroid resistance to Anopheles gambiae.

6 required for efficient Plasmodium killing in Anopheles gambiae.

7 munity that enhance nitric oxide toxicity in Anopheles gambiae.

8 genic mosquitoes of the human malaria vector Anopheles gambiae.

9 s an active toxin for larvae of the mosquito Anopheles gambiae.

10 ire compared with those of Aedes aegypti and Anopheles gambiae.

11 the size of the genome of the malaria vector Anopheles gambiae.

12 n the genomes of Drosophila melanogaster and Anopheles gambiae.

13 ut are randomly distributed in the genome of Anopheles gambiae.

14 fly Drosophila melanogaster and the mosquito Anopheles gambiae.

15 odium was investigated in the malaria vector Anopheles gambiae.

16 enes in 13 fruitfly species and the mosquito Anopheles gambiae.

17 d Drosophila pseudoobscura, and the mosquito Anopheles gambiae.

18 ologous loci in the distant mosquito genome, Anopheles gambiae.

19 genes in the early embryos of the mosquito, Anopheles gambiae.

20 ceptionally poorly conserved in the mosquito Anopheles gambiae.

21 frican malaria vectors, such as the mosquito Anopheles gambiae.

22 cturally diverse compounds against Orco from Anopheles gambiae.

23 Ago1 is the predominant carrier of miRNAs in Anopheles gambiae.

24 ene drive (SDGD) in the human malaria vector Anopheles gambiae.

25 larvae of the mosquitoes, Aedes aegypti and Anopheles gambiae.

26 uestions regarding SGs of the malaria vector Anopheles gambiae.

27 IIS6, in pyrethroid-resistant populations of Anopheles gambiae.

28 hila melanogaster (D. mel.) and the mosquito Anopheles gambiae (A. gam.), the midline is narrow and s

29 In Anopheles gambiae, a likely candidate for sexual selecti

30 Anopheles gambiae, a major vector of malaria, is a compl

31 The purine salvage pathway of Anopheles gambiae, a mosquito that transmits malaria, ha

32 ntains genome information for two organisms: Anopheles gambiae, a vector for the Plasmodium protozoan

33 eding arthropods, Pediculus humanus humanus, Anopheles gambiae, Aedes Aegypti and Culex pipiens quinq

34 Draft genome sequences are available for Anopheles gambiae, Aedes aegypti, and Culex quinquefasci

35 but that an adjacent region has expanded in Anopheles gambiae, Aedes aegypti, and Tribolium castaneu

36 immune repertoire: in Aa, the malaria vector Anopheles gambiae (Ag), and the fruit fly Drosophila mel

37 ng available sequences from D. melanogaster, Anopheles gambiae (Ag), Caenorhabditis elegans (Ce), the

38 tor coreceptor of the African malaria vector Anopheles gambiae (AgamORco) in a small collection of na

39 The PNP from Anopheles gambiae (AgPNP) was expressed in Escherichia c

40 diator of heat seeking in the malaria vector Anopheles gambiae Although Ir21a mediates heat avoidance

41 port on the molecular characterization of an Anopheles gambiae aminopeptidase N (AgAPN1) as the predo

42 f a survey of 1280 genomes of the mosquitoes Anopheles gambiae, An. coluzzii, and Aedes aegypti in wh

43 % of which have their closest counterpart in Anopheles gambiae and 21% have highest similarity with o

44 nophelines were collected, of which 388 were Anopheles gambiae and 629 An. ziemanni.

45 mall D7 family of the African malaria vector Anopheles gambiae and a D7 long form from Aedes aegypti

46 the closely related African malaria vectors Anopheles gambiae and A. arabiensis.

47 Anopheles gambiae and A. stephensi larvae were bred unde

48 e-domain and one two-domain D7 proteins from Anopheles gambiae and Aedes aegypti (AeD7), respectively

49 Anopheles gambiae and Aedes aegypti are perhaps the best

50 Anopheles gambiae and Aedes aegypti have evolved a stron

51 file the transcriptomes of 8506 hemocytes of Anopheles gambiae and Aedes aegypti mosquito vectors.

52 e most important vectors of human pathogens (Anopheles gambiae and Aedes aegypti) imbibing multiple b

53 essential AChE1 enzymes from the mosquitoes Anopheles gambiae and Aedes aegypti.

54 Anopheles gambiae and An. arabiensis are major malaria v

55 Male hybrids between Anopheles gambiae and An. arabiensis suffer from hybrid

56 b-Saharan Africa, two major malaria vectors, Anopheles gambiae and An. coluzzii, breed in distinct la

57 of key vector species from Africa and Asia (Anopheles gambiae and An. stephensi) to transmit the hum

58 cts populations of the major malaria vectors Anopheles gambiae and Anopheles coluzzii in Burkina Faso

59 They include the African malaria vectors Anopheles gambiae and Anopheles coluzzii, as well as Aed

60 f Plasmodium berghei and Plasmodium vivax to Anopheles gambiae and Anopheles dirus, respectively.

61 s after initiation of treatment to determine Anopheles gambiae and Anopheles funestus survival and in

62 he last 3 y in the two major malaria vectors Anopheles gambiae and Anopheles funestus, with a higher

63 -kDa) protein related to the gSG7 protein of Anopheles gambiae and Anopheles stephensi Recombinant al

64 ploying two different species of mosquitoes, Anopheles gambiae and Anopheles stephensi.

65 rized membrane-bound midgut glycoproteins in Anopheles gambiae and Anopheles stephensi.

66 the lifecycle of the malaria vector mosquito Anopheles gambiae and are initiated by peripheral signal

67 uts in an area of Benin where the mosquitoes Anopheles gambiae and Culex quinquefasciatus are resista

68 n for three mosquito species: Aedes aegypti, Anopheles gambiae and Culex quinquefasciatus, a body lou

69 ergence between the lineages of the mosquito Anopheles gambiae and D. melanogaster involved an extens

70 ctory sensory neurons to attractive odors in Anopheles gambiae and Drosophila melanogaster.

71 andidate genes were successfully cloned from Anopheles gambiae and expressed in insect cells.

72 FREP1) is critical for parasite infection in Anopheles gambiae and facilitates Plasmodium invasion in

73 lycans along the apical midgut microvilli of Anopheles gambiae and further demonstrated ookinete reco

74 ersion 2La from the principal malaria vector Anopheles gambiae and its relatives in the A. gambiae co

75 residues of the ortholog of human ICMT from Anopheles gambiae and observed reduced or undetectable c

76 ed Dorsal target enhancers from the mosquito Anopheles gambiae and the flour beetle Tribolium castane

77 osophila pseudoobscura, the malaria mosquito Anopheles gambiae and the yellow fever mosquito Aedes ae

78 gen vectors such as the malaria-transmitting Anopheles gambiae and to correct deleterious mutations i

79 g in two other mosquitoes (Culex pipiens and Anopheles gambiae) and the bed bug, Cimex lectularius, s

80 are available for 3 species, Aedes aegypti, Anopheles gambiae, and Culex quinquefasciatus (Diptera:

81 biology of two SGSs in the malaria mosquito, Anopheles gambiae, and demonstrate their involvement in

82 ated with Plasmodium falciparum infection in Anopheles gambiae, and FREP1 is important for Plasmodium

83 etected in the major African malaria vector, Anopheles gambiae, and has been attributed to a combinat

84 main, ZLD orthologs from Drosophila virilis, Anopheles gambiae, and Nasonia vitripennis activate tran

85 ae of the mosquitoes Culex quinquefasciatus, Anopheles gambiae, and Ochlerotatus triseriatus.

86 cificity of P47Rec from distant anophelines (Anopheles gambiae, Anopheles dirus, and Anopheles albima

87 al kinase (JNK) pathway is a key mediator of Anopheles gambiae antiplasmodial responses to P. falcipa

88 t sites (TSSs) in D. melanogaster but not in Anopheles gambiae, Apis mellifera, or Tribolium castaneu

89 largely sympatric molecular forms M and S of Anopheles gambiae appears mostly limited to division 6 a

90 The Y chromosome of the human malaria vector Anopheles gambiae appears to be involved in sex determin

91 mately 13,000 genes listed in VectorBase for Anopheles gambiae are predictions that have still not be

92 The M and S molecular forms of Anopheles gambiae are undergoing speciation as they adap

93 sitol-specific phospholipase C (PI-PLC) from Anopheles gambiae BBMV was extracted by Cry11Ba bound to

94 A genetically selected refractory strain of Anopheles gambiae blocks Plasmodium development, melaniz

95 natural populations of the malaria mosquito Anopheles gambiae, blood-fed females direct nutritional

96 nthetically in the main human malaria vector Anopheles gambiae, by selectively destroying the X-chrom

97 The RNAi pathway in Anopheles gambiae can be silenced by transfecting cells

98 ne from the gut-specific and blood-inducible Anopheles gambiae carboxypeptidase (AgCP) promoter.

99 ective pressures on the major malaria vector Anopheles gambiae, caused by the widespread use of insec

100 NAi-mediated depletion of Kto and Skd in the Anopheles gambiae cell line L5-3 resulted in a decrease

101 y the temporal transcription responses of an Anopheles gambiae cell line upon challenge with multiple

102 expression in immortalized A. stephensi and Anopheles gambiae cell lines in vitro and in A. stephens

103 of mosquitoes (all p<0.0001), especially the Anopheles gambiae complex (relative rate [RR] 0.23; 95%

104 resistance phenotypes in mosquitoes from the Anopheles gambiae complex across Africa.

105 ga-Mali) was identified in mosquitoes of the Anopheles gambiae complex collected in the Malian villag

106 Mosquitoes in the Anopheles gambiae complex show rapid ecological and beha

107 n male mating behavior, recent data from the Anopheles gambiae complex suggests that, apart from the

108 Mosquitoes of the Anopheles gambiae complex were identified to species usi

109 As with members of the Anopheles gambiae complex, An. funestus shows marked gen

110 However, in the Anopheles gambiae complex, the primary African vectors o

111 cur in all intercrosses among members of the Anopheles gambiae complex.

112 nces restricted to the member species of the Anopheles gambiae complex.

113 ulations of the major African malaria vector Anopheles gambiae Contact with LLINs reduced the immedia

114 genome of the major malaria vector mosquito Anopheles gambiae contains at least seven putative AQP s

115 he karyotype of the African malaria mosquito Anopheles gambiae contains two pairs of autosomes and a

116 The African malaria mosquito, Anopheles gambiae, contains over 30 families of IS630/Tc

117 of an Orco family agonist, VUAA1, using the Anopheles gambiae coreceptor (AgOrco) and other ortholog

118 reconstruct the phylogenetic history of the Anopheles gambiae cryptic species complex have yielded s

119 three major disease-transmitting mosquitoes: Anopheles gambiae, Culex quinquefasciatus and A. aegypti

120 ocidal to important vector species including Anopheles gambiae, Culex quinquefasciatus, and Aedes aeg

121 50s associated with pyrethroid resistance in Anopheles gambiae (CYPs 6M2, 6P3, 6P4, 6P5, 9J5, 9K1, 6Z

122 atment to deplete phagocytic immune cells in Anopheles gambiae, demonstrating the role of phagocytes

123 used quantitative PCR to assess whether the Anopheles gambiae densonucleosis virus (AgDNV) had poten

124 We developed and characterized an efficient Anopheles gambiae densovirus (AgDNV) over-expression sys

125 nsects, such as the malaria vector mosquito, Anopheles gambiae, depend upon chemoreceptors to respond

126 transmission by the African mosquito vector Anopheles gambiae depends on finely tuned vector-parasit

127 e monitored miRNA expression in the mosquito Anopheles gambiae during the 72-h period immediately aft

128 Plasmodium falciparum infects Anopheles gambiae efficiently at low densities (4% mosqu

129 The high-affinity adenosine kinase from Anopheles gambiae efficiently converts adenosine to aden

130 ays were performed with isolated serosa from Anopheles gambiae embryos.

131 ed heme peroxidase is required for long-term Anopheles gambiae fertility.

132 Gene flow was investigated in Anopheles gambiae from eight localities that span the ec

133 This family is also present in the Anopheles gambiae genome and displays remarkable synteny

134 We explored the Anopheles gambiae genome for the presence of satellite r

135 collaborative effort, the first draft of the Anopheles gambiae genome sequence and its preliminary an

136 w c-type lysozyme genes were found using the Anopheles gambiae genome sequence, increasing to eight t

137 The Anopheles gambiae genome will enable identification of n

138 sts data for nine genomes: mosquitoes (three Anopheles gambiae genomes, Aedes aegypti and Culex quinq

139 ons populate the Drosophila melanogaster and Anopheles gambiae genomes, use a transposase that is not

140 p includes proteins from insects such as the Anopheles gambiae GNBP subgroup B for which a catalytic

141 In both D. melanogaster and Anopheles gambiae, GstD1 has been implicated in the resi

142 Aedes aegypti and Anopheles gambiae harbor the causative agents of disease

143 the distribution of paracentric inversions, Anopheles gambiae has been subdivided into five subspeci

144 The mosquito Anopheles gambiae has heteromorphic sex chromosomes, whi

145 odel for the enzyme from the malaria vector, Anopheles gambiae, has been shown to cycle in catalysis

146 related (D7r) proteins of the malaria vector Anopheles gambiae have been shown to bind the biogenic a

147 The M and S forms of Anopheles gambiae have been the focus of intense study b

148 ican malaria vectors, Anopheles coluzzii and Anopheles gambiae, have been attributed to assortative m

149 The functions of five Anopheles gambiae homologs were tested by using RNAi to

150 PHs) are positive and negative regulators of Anopheles gambiae immune responses mediated by the compl

151 we show evidence of Wolbachia infections in Anopheles gambiae in Burkina Faso, West Africa.

152 a hybrid zone between Anopheles coluzzii and Anopheles gambiae in Guinea-Bissau, where high hybridisa

153 of the Afrotropical malaria vector mosquito Anopheles gambiae in the labellum at the tip of the prob

154 ne expression to develop transgenic lines of Anopheles gambiae in which olfactory receptor neurons ex

155 the dispersal of its most efficient vector, Anopheles gambiae, in order to target interventions and

156 the principal role of hormonal signaling in Anopheles gambiae initiated shortly after blood-feeding,

157 Resistance to pyrethroids in the mosquito Anopheles gambiae is a growing problem.

158 Anopheles gambiae is a highly anthropophilic mosquito re

159 Anopheles gambiae is a major malaria vector in Africa an

160 Anopheles gambiae is a major mosquito vector responsible

161 Anopheles gambiae is a major vector mosquito for Plasmod

162 The mosquito Anopheles gambiae is a primary vector of Plasmodium para

163 revealed that the single hodor orthologue in Anopheles gambiae is an essential gene.

164 The African malaria mosquito Anopheles gambiae is diversifying into ecotypes known as

165 The bursicon gene in Anopheles gambiae is encoded by two loci.

166 9-based homing system for the suppression of Anopheles gambiae is encouraging; however, with current

167 ere, we show that the primary malaria vector Anopheles gambiae is targeted and killed by small insect

168 f the R7 photoreceptors in Aedes aegypti and Anopheles gambiae is the extreme apical projection of th

169 The mosquito Anopheles gambiae is the major vector of malaria in sub-

170 Anopheles gambiae is the mosquito vector responsible for

171 The mosquito Anopheles gambiae is the principal Afrotropical vector f

172 The malaria vector, Anopheles gambiae, is associated with a latitudinal clin

173 The Anopheles gambiae L3-5 refractory (R) line melanizes mos

174 midgut cadherin AgCad1 cDNA was cloned from Anopheles gambiae larvae and analyzed for its possible r

175 cDNA (AgALP1) was cloned from the midgut of Anopheles gambiae larvae.

176 African vector, Anopheles coluzzii (formerly Anopheles gambiae M).

177 a domestica house fly), their role as pests (Anopheles gambiae malaria mosquito), and their value as

178 Pyrethroid resistant Anopheles gambiae malaria vectors are widespread through

179 parated four distinct cell lineages from the Anopheles gambiae male gonads: premeiotic, meiotic (prim

180 hough the presence of Pe. chrysogenum in the Anopheles gambiae midgut does not affect mosquito surviv

181 We show that a peroxidase, secreted by the Anopheles gambiae midgut, and dual oxidase form a dityro

182 termine the antiviral immune pathways of the Anopheles gambiae midgut, the initial site of viral infe

183 e areas is reviewed, with an emphasis on the Anopheles gambiae model.

184 nvestigate the function of P. berghei P47 in Anopheles gambiae mosquito infections.

185 The reproductive fitness of the Anopheles gambiae mosquito represents a promising target

186 he microbial community within the gut of the Anopheles gambiae mosquito, a major malaria vector in Af

187 The Anopheles gambiae mosquito, which is the vector for Plas

188 Anopheles gambiae mosquitoes are major African vectors o

189 Anopheles gambiae mosquitoes are the most important vect

190 Plasmodium falciparum transmission by Anopheles gambiae mosquitoes is remarkably efficient, re

191 A study of Anopheles gambiae mosquitoes shows that a molecule invol

192 e rapidly and completely blocked when female Anopheles gambiae mosquitoes take up low concentrations

193 ntified two quantitative trait loci (QTL) in Anopheles gambiae mosquitoes that confer refractoriness

194 Anopheles gambiae mosquitoes that transmit Plasmodium fa

195 ingested blood enhance the susceptibility of Anopheles gambiae mosquitoes to malaria infection by dis

196 Exposure of Anopheles gambiae mosquitoes to Plasmodium infection enh

197 Here Anopheles gambiae mosquitoes, the primary malarial vecto

198 be a powerful molecular tool for research in Anopheles gambiae mosquitoes.

199 . bacterium was isolated from the midguts of Anopheles gambiae mosquitoes.

200 nd Plasmodium berghei expressing PfCelTOS in Anopheles gambiae mosquitoes.

201 asite to evade the mosquito immune system of Anopheles gambiae mosquitoes.

202 Here we show that the Anopheles gambiae noncatalytic serine protease CLIPA8, a

203 ing pockets of odorant binding proteins from Anopheles gambiae (OBP1 and OBP47) were analysed using i

204 nal analysis across much of the conventional Anopheles gambiae odorant receptor (AgOR) repertoire was

205 Here we functionally characterize the Anopheles gambiae odorant receptor (AgOr) repertoire.

206 iled analysis of the resistance situation in Anopheles gambiae on Bioko Island after pyrethroid resis

207 bing miRNAs in the African malaria mosquito, Anopheles gambiae, on the basis of similarity to known m

208 In Anopheles gambiae, ookinete invasion elicited similar re

209 Plasmodium falciparum and the insect vector Anopheles gambiae paves the way for scientists to study

210 ory system in Plasmodium falciparum infected Anopheles gambiae, Plasmodium berghei infected Anopheles

211 s application using genome variation data of Anopheles gambiae, Plasmodium falciparum and Plasmodium

212 In the malaria mosquito Anopheles gambiae polymorphic chromosomal inversions may

213 We surveyed an Anopheles gambiae population in a West African malaria t

214 throid resistance in various Ae. aegypti and Anopheles gambiae populations around the world.

215 h Plasmodium falciparum infection in natural Anopheles gambiae populations at malaria endemic areas i

216 h previously described mating preferences of Anopheles gambiae populations could be exploited to mani

217 resistance and its underlying mechanisms in Anopheles gambiae populations from a subset of trial vil

218 allele size data for a group of West African Anopheles gambiae populations.

219 Here we show that the Anopheles gambiae protein AgOr1, a female-specific membe

220 In the African malaria vector, Anopheles gambiae quantitative and qualitative variance

221 This analysis of the Anopheles gambiae receptors permits a comparison with th

222 the gene homologous to Drosophila Dl and to Anopheles gambiae REL1 (Gambif1) from the yellow fever m

223 Afrotropical human malaria vector mosquito, Anopheles gambiae, remains a significant threat to globa

224 e mechanisms in the principle malaria vector Anopheles gambiae, remains largely uncharacterized in Bu

225 Our analysis of the Anopheles gambiae repertoire identifies receptors that m

226 ot competitively linked to processes shaping Anopheles gambiae reproduction.

227 Tracking multiple free-flying Anopheles gambiae responding to human-occupied bed nets

228 Anopheles gambiae, responsible for the majority of malar

229 een carbamate and pyrethroid resistance with Anopheles gambiae s.l.

230 he probability that pyrethroid resistance in Anopheles gambiae s.l. exceeds the World Health Organiza

231 ll this knowledge gap, coupled and uncoupled Anopheles gambiae s.l. males (all M form (Anopheles colu

232 distribution of Herves in six populations of Anopheles gambiae s.s.

233 Anopheles gambiae s.s. mosquitoes are efficient vectors

234 Here, we show that the attraction of Anopheles gambiae s.s. to plant odors increased by 30% a

235 d to assess the safety and immunogenicity of Anopheles gambiae saliva vaccine (AGS-v), a peptide-base

236 ssed by passive case detection and number of Anopheles gambiae sensu lato mosquitoes collected per li

237 mary endpoints included the number of female Anopheles gambiae sensu lato mosquitoes collected per tr

238 Of 1494 female Anopheles (89.8% Anopheles gambiae sensu lato), 88.3% were fed, 51.9% had

239 , the seasonal cycles of Anopheles coluzzii, Anopheles gambiae sensu stricto (s.s.), and Anopheles ar

240 iphenyltrichloroethane (DDT) in field-caught Anopheles gambiae sensu stricto homozygous for the kdr m

241 Anopheles gambiae sensu stricto is the most important ve

242 he prevailing wind direction included 81,000 Anopheles gambiae sensu stricto, 6 million A. coluzzii a

243 The Afrotropical mosquito Anopheles gambiae sensu stricto, a major vector of malar

244 that in the primary African malaria vector, Anopheles gambiae sensu stricto, a single enzyme, CYP6M2

245 ssays were conducted using laboratory-reared Anopheles gambiae sensu stricto.

246 ce of an opal codon between nsP3 and nsP4 in Anopheles gambiae, sequence analysis of ONNV RNA extract

247 ng species within the primary malaria vector Anopheles gambiae show different ecological preferences

248 Gene expression in Anopheles gambiae shows a deficiency of testis-expressed

249 After injection into adult Anopheles gambiae, some strains of Wolbachia invade the

250 nversion is a widespread polymorphism in the Anopheles gambiae species complex, the major African mos

251 genomic islands of divergence separating the Anopheles gambiae species pair.

252 re present in the distantly-related Dipteran Anopheles gambiae, suggesting that the properties of spe

253 bosomal gene sequences of the malaria vector Anopheles gambiae that are located exclusively on the mo

254 We have identified 156 genes in Anopheles gambiae that code for putative cuticular prote

255 rotein from the major African malaria vector Anopheles gambiae that specifically, tightly, and quickl

256 nding site of an OR from the malaria vector, Anopheles gambiae The closely related odorant-specificit

257 or molecules to the malaria vector mosquito, Anopheles gambiae The drive system targets the cardinal

258 s have been identified in the malaria vector Anopheles gambiae, the crystal structures of only six of

259 ructs that function as gene drive systems in Anopheles gambiae, the main vector for malaria.

260 he serpin (SRPN) gene family in the mosquito Anopheles gambiae, the major malaria vector in Sub-Sahar

261 ss of selection for pyrethroid resistance in Anopheles gambiae, the most important malaria vector in

262 Anopheles gambiae, the most important vector of human ma

263 Anopheles gambiae, the primary African vector of malaria

264 After 24 h, the mortality of Anopheles gambiae, the principal African malaria vector,

265 In Anopheles gambiae, the ribozymes were found differential

266 hila species, and between species related to Anopheles gambiae, the vector of malignant malaria in Af

267 sects, including the malaria vector mosquito Anopheles gambiae; the silk moth, Bombyx mori; and the t

268 ium infection, through target populations of Anopheles gambiae, thereby disabling the mosquito's abil

269 In the African malaria mosquito, Anopheles gambiae, this is complemented by a strong publ

270 actometer, we investigated the attraction of Anopheles gambiae to 50 Kenyan children (aged 5-12 years

271 anges in species composition from endophilic Anopheles gambiae to exophilic An. arabiensis.

272 Resistance in Anopheles gambiae to members of all 4 major classes (pyr

273 suppressors of the melanization responses of Anopheles gambiae to Plasmodium berghei (murine malaria)

274 ive contribution of AgTRIO to the ability of Anopheles gambiae to transmit Plasmodium berghei to mice

275 ngs of heterologously expressed and purified Anopheles gambiae TRPA1 (AgTRPA1), with and without the

276 In contrast to Drosophila TRPA1, Anopheles gambiae TRPA1 is directly and potently activat

277 ect species (three species of Drosophila and Anopheles gambiae), two species of Caenorhabditis, and s

278 We show that in the mosquito Anopheles gambiae, two such proteins that antagonize mal

279 ding insects, including the malaria mosquito Anopheles gambiae, use highly specialized and sensitive

280 ous SRPN6 genes from Anopheles stephensi and Anopheles gambiae using phylogenetic, molecular, reverse

281 squitoes, including the major malaria vector Anopheles gambiae, utilize carbon dioxide (CO(2)) and 1-

282 icide resistance in the major malaria vector Anopheles gambiae was assessed.

283 Anopheles gambiae was genetically partitioned into inlan

284 Recently, TEP1 from the malarial vector Anopheles gambiae was shown to mediate recognition and k

285 island (PRI) of the African mosquito vector, Anopheles gambiae, was mapped to five genomic regions co

286 ome of the primary African malaria mosquito, Anopheles gambiae We find that the An. gambiae Y consist

287 rated in Caenorhabditis elegans and later in Anopheles gambiae, we show here that an acellular gut ba

288 site, Plasmodium falciparum, and its vector, Anopheles gambiae, were published.

289 oding cDNA from the malaria vector mosquito, Anopheles gambiae, where olfaction is critical for vecto

290 ble exception is the female malaria mosquito Anopheles gambiae, which after sex loses her susceptibil

291 Anopheles gambiae, which has been the major mosquito vec

292 n applied widely to the major malaria vector Anopheles gambiae, which has proved more difficult to ge

293 res of the flies Drosophila melanogaster and Anopheles gambiae, which have 62 and 79 Ors respectively

294 le, ITmD37E sequences from Aedes aegypti and Anopheles gambiae, which have an estimated common ancest

295 applied our method to predict 200 miRNAs in Anopheles gambiae, which is the most important vector of

296 sistance markers in the major malaria vector Anopheles gambiae, which we used to screen mosquitoes fr

297 of Aedes aegypti and 52% larger than that of Anopheles gambiae with multiple gene-family expansions,

298 pattern recognition receptor gene family in Anopheles gambiae, with as many as 59 putative members,

299 repeats, located in a single cluster on the Anopheles gambiae X chromosome.

300 ob, for the M factor in the malaria mosquito Anopheles gambiae Yob, activated at the beginning of zyg