ライフサイエンスコーパス: Anopheles gambiae

1 munity that enhance nitric oxide toxicity in Anopheles gambiae.

2 genic mosquitoes of the human malaria vector Anopheles gambiae.

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

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

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

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

7 n the genomes of Drosophila melanogaster and Anopheles gambiae.

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

9 fly Drosophila melanogaster and the mosquito Anopheles gambiae.

10 uestions regarding SGs of the malaria vector Anopheles gambiae.

11 odium was investigated in the malaria vector Anopheles gambiae.

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

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

14 d Drosophila pseudoobscura, and the mosquito Anopheles gambiae.

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

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

17 ceptionally poorly conserved in the mosquito Anopheles gambiae.

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

19 named Maque in the African malaria mosquito, Anopheles gambiae.

20 of a serine protease gene from the mosquito Anopheles gambiae.

21 Dox-A2 and 93% with its putative ortholog in Anopheles gambiae.

22 as isolated from the malaria vector mosquito Anopheles gambiae.

23 lower dipteran insect, the malaria mosquito Anopheles gambiae.

24 phisms for the African human malaria vector, Anopheles gambiae.

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

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

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

28 pression system for the major malaria vector Anopheles gambiae.

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

30 required for efficient Plasmodium killing in Anopheles gambiae.

31 d transposon in which an engrailed cDNA from Anopheles gambiae (a mosquito) is expressed from a Droso

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

33 In Anopheles gambiae, a likely candidate for sexual selecti

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

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

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

37 cDNA encoding a putative PM protein, termed Anopheles gambiae adult peritrophin 1 (Ag-Aper1).

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

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

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

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

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

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

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

45 % of which have their closest counterpart in Anopheles gambiae and 21% have highest similarity with o

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

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

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

49 Anopheles gambiae and A. stephensi larvae were bred unde

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

51 Anopheles gambiae and Aedes aegypti have evolved a stron

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 mosquito specie

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 els of gene flow between the sibling species Anopheles gambiae and Anopheles arabiensis, similar to e

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

65 ploying two different species of mosquitoes, 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 the GST-2 subfamily from insects, including Anopheles gambiae and Drosophila melanogaster.

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 roup; Anopheles albitarsis, Anopheles dirus, Anopheles gambiae, Anopheles nuneztovari, Anopheles pseu

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 class I glutathione S-transferases (GSTs) of Anopheles gambiae are encoded by a complex gene family.

92 Pase-overexpressing cells in Ae. aegypti and Anopheles gambiae are localized at the posterior part of

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

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

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

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

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

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

99 discovered in the African malaria mosquito, Anopheles gambiae, by using new software designed to rap

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

101 ing 3.4-kb DNA fragment at the 5' end of the Anopheles gambiae carboxypeptidase (AgCP) gene were link

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

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

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

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

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

107 The population structure of the Anopheles gambiae complex is unusual, with several sibli

108 n agriculture and the diversification of the Anopheles gambiae complex of mosquito vectors.

109 The African Anopheles gambiae complex of six sibling species has man

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

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

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

113 Of the seven recognized species of the Anopheles gambiae complex, A. gambiae s.s. is the most w

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

115 nversion called the 2La that is found in the Anopheles gambiae complex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

132 ictus C6/36 cells by electroporation or into Anopheles gambiae embryos by biolistic particle bombardm

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

134 xpressed specifically in the midgut of adult Anopheles gambiae females.

135 criptome of the major African malaria vector Anopheles gambiae for immune response genes in adult fem

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

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

138 We have searched the Anopheles gambiae genome for members of the three major

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

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

141 The Anopheles gambiae genome sequence, coupled with the Dros

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

143 The Anopheles gambiae genome will enable identification of n

144 G protein-coupled receptors (GPCRs) from the Anopheles gambiae genome.

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

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

147 Chromosomal forms of Anopheles gambiae, given the informal designations Bamak

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

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

150 he elucidation of digestive processes in the Anopheles gambiae gut leading to the utilization of the

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

152 The mosquito Anopheles gambiae has heteromorphic sex chromosomes, whi

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

154 analysis of the major human malaria vector, Anopheles gambiae, has revealed natural factors that red

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

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

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

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

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

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

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

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

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

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

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

166 Anopheles gambiae is a highly anthropophilic mosquito re

167 Anopheles gambiae is a major malaria vector in Africa an

168 Anopheles gambiae is a major mosquito vector responsible

169 Anopheles gambiae is a major vector mosquito for Plasmod

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

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

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

173 9-based homing system for the suppression of Anopheles gambiae is encouraging; however, with current

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

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

176 Anopheles gambiae is the mosquito vector responsible for

177 Anopheles gambiae is the primary vector of human malaria

178 The mosquito Anopheles gambiae is the principal Afrotropical vector f

179 Anopheles gambiae is the principal vector of malaria, a

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

181 The African malaria mosquito, Anopheles gambiae, is specialized for rapid completion o

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

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

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

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

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

187 Pyrethroid resistant Anopheles gambiae malaria vectors are widespread through

188 A Plasmodium-refractory strain of Anopheles gambiae melanotically encapsulates many specie

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

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

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

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

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

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

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

196 Anopheles gambiae mosquitoes are major African vectors o

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

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

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

200 Anopheles gambiae mosquitoes that transmit Plasmodium fa

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

202 Exposure of Anopheles gambiae mosquitoes to Plasmodium infection enh

203 Here Anopheles gambiae mosquitoes, the primary malarial vecto

204 nd Plasmodium berghei expressing PfCelTOS in Anopheles gambiae mosquitoes.

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

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

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

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

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

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

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

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

213 In Anopheles gambiae, ookinete invasion elicited similar re

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

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

216 In the malaria mosquito Anopheles gambiae polymorphic chromosomal inversions may

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

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

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

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

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

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

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

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

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

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

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

228 omes of Plasmodium falciparum and its vector Anopheles gambiae represent a big step toward the discov

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

230 Anopheles gambiae, responsible for the majority of malar

231 roach to empirical data from locus AG2H46 of Anopheles gambiae resulted in a significant excess of si

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

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

234 Anopheles gambiae s.s. mosquitoes are efficient vectors

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

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 transmission by the malaria vector mosquito Anopheles gambiae sensu stricto (henceforth A. gambiae).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

258 Anopheles gambiae, the most important vector of human ma

259 Anopheles gambiae, the primary African vector of malaria

260 n of heterologous genes in cultured cells of Anopheles gambiae, the principle mosquito vector respons

261 In Anopheles gambiae, the ribozymes were found differential

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

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

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

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

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

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

268 cally important mosquito, the malaria vector Anopheles gambiae, to determine how this dipteran insect

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

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

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

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

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

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

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

276 Genetic variation of Anopheles gambiae was analysed to assess interpopulation

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

278 Anopheles gambiae was genetically partitioned into inlan

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

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

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

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

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

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

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

286 Anopheles gambiae, which has been the major mosquito vec

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

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

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

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

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

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

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