ライフサイエンスコーパス: Drosophila melanogaster

1 nsport of proteins in male and female flies (Drosophila melanogaster).

2 as invertebrates (Caenorhabditis elegans and Drosophila melanogaster).

3 mutations in ribosomal protein (Rp) genes in Drosophila melanogaster.

4 bodies from the first instar larva and adult Drosophila melanogaster.

5 incompatibilities (EGIs) in the model insect Drosophila melanogaster.

6 d, and compared with data on a population of Drosophila melanogaster.

7 to-cell heterogeneity in their expression in Drosophila melanogaster.

8 ageing in the antennal ears of the fruit fly Drosophila melanogaster.

9 mal organ size, regulates ovariole number in Drosophila melanogaster.

10 tion library for a developmental enhancer in Drosophila melanogaster.

11 hod for a low input sample, a single outbred Drosophila melanogaster.

12 we conducted a genetic suppressor screen in Drosophila melanogaster.

13 enance of male germline stem cells (GSCs) in Drosophila melanogaster.

14 the transition between hunger and satiety in Drosophila melanogaster.

15 disclosed a new in vivo function for USEs in Drosophila melanogaster.

16 resembles that of standard homing drives in Drosophila melanogaster.

17 zog (CG5830), through a multimodal screen in Drosophila melanogaster.

18 fected cells and to drive hyperlocomotion in Drosophila melanogaster.

19 anisms, including Caenorhabditis elegans and Drosophila melanogaster.

20 ring, is based on replication competition in Drosophila melanogaster.

21 dressed for small animals including the fly, Drosophila melanogaster.

22 insights into ovariole number regulation in Drosophila melanogaster.

23 ent changes in the metabolomes of long-lived Drosophila melanogaster.

24 e genes in their original genomic context in Drosophila melanogaster.

25 and female responses to dietary variation in Drosophila melanogaster.

26 Here, we address these problems using Drosophila melanogaster.

27 isease, we utilized a new, allelic series of Drosophila melanogaster.

28 the neuroprotective effects of PI3K in adult Drosophila melanogaster.

29 ressed bitter gustatory receptors (Grs) from Drosophila melanogaster.

30 largely unknown, even for the model species Drosophila melanogaster.

31 evoid of lamin and nuclear pore complexes in Drosophila melanogaster.

32 ions that give rise to the sensory organs of Drosophila melanogaster.

33 y this fundamental problem, we used the fly, Drosophila melanogaster.

34 ry that links egg laying to mating status in Drosophila melanogaster.

35 properties of the early olfactory system of Drosophila melanogaster.

36 of identified cell types in the HD system of Drosophila melanogaster.

37 ne neurons that predict behavioral choice in Drosophila melanogaster.

38 hygrosensory, and memory systems in the fly Drosophila melanogaster.

39 ents mating decisions in the brain of female Drosophila melanogaster.

40 erization of candidates were performed using Drosophila melanogaster.

41 ins, we screened for genetic interactions in Drosophila melanogaster.

42 es in behaviour compared to its close cousin Drosophila melanogaster(6,7), which are linked to its ex

43 Drosophila melanogaster, a fruit fly, is an exquisite mo

44 cting PCB metabolism and toxicity, we tested Drosophila melanogaster, a well-known model system for g

45 s like the mammalian prostate and the paired Drosophila melanogaster accessory glands secrete seminal

46 sotope-resolved metabolomics to show that in Drosophila melanogaster, Acetobacter pomorum (Ap) and La

47 Here, we show that in Drosophila melanogaster, activation of a subset of serot

48 s (Oga(D133N) and Oga(KO) , respectively) in Drosophila melanogaster Adult Oga(D133N) and Oga(KO) fli

49 ypes associated with beta5 overexpression in Drosophila melanogaster adults.

50 A polymerase II CTD phosphatase (Ssu72, from Drosophila melanogaster), an essential CTD phosphatase t

51 impacts of imidacloprid are investigated in Drosophila melanogaster, an experimental organism expose

52 s) genome-wide in mammalian cells as well as Drosophila melanogaster and Caenorhabditis elegans, indi

53 the traditional biomedical models zebrafish, Drosophila melanogaster and Caenorhabditis elegans, whic

54 Here, we used the powerful genetics of Drosophila melanogaster and developed an in vivo assay t

55 ram and single sensillum recordings in adult Drosophila melanogaster and inhibited OR-mediated olfact

56 we discuss aspects of the circadian clock in Drosophila melanogaster and mammals, including the compo

57 rly or late in life, of both male and female Drosophila melanogaster and measure the effects on court

58 pressing it in the indirect flight muscle of Drosophila melanogaster and measuring alterations to mus

59 , enabling reconstruction of dense wiring in Drosophila melanogaster and mouse nervous tissue.

60 We purified the three SARAH domains from Drosophila melanogaster and performed an unbiased pulldo

61 functions have been extensively explored in Drosophila melanogaster and some other Dipteran species,

62 Here, we employ Drosophila melanogaster and the LacI/lacO system to inve

63 mulated data (calibrated from experiments on Drosophila melanogaster) and real data from five distinc

64 In human (Homo sapiens), fruit fly (Drosophila melanogaster), and yeast (Saccharomyces cerev

65 pathway has only been fully characterized in Drosophila melanogaster, and apoptosis-related proteins

66 tion-level data from a Zambian population of Drosophila melanogaster, and find that it has experience

67 Using the well-established Drosophila melanogaster animal model to study sleep [3],

68 ports have demonstrated that the fruit flies Drosophila melanogaster are capable of visual cue-driven

69 he Hippo pathway was initially discovered in Drosophila melanogaster as a key regulator of tissue gro

70 The use of adult Drosophila melanogaster as a model for hematopoiesis or

71 c growth using the neuromuscular junction of Drosophila melanogaster as a model system.

72 We use the grooming behavior of Drosophila melanogaster as a model to investigate the se

73 platform to study LGMD2H pathogenesis using Drosophila melanogaster as a model.

74 t advances in neurogenetics have highlighted Drosophila melanogaster as an exciting model to study ne

75 Here we use Drosophila melanogaster as an in vivo model to investiga

76 We also show that in Drosophila melanogaster as gene expression increases, a

77 unity of researchers that use the fruit fly, Drosophila melanogaster, as a model organism.

78 compounds were found to be nonmutagenic in a Drosophila melanogaster assay and exhibited a promising

79 ccessible method for non-invasive imaging of Drosophila melanogaster at high resolution using micro-c

80 res of human SERINC5 and its orthologue from Drosophila melanogaster at subnanometer and near-atomic

81 he whole adult brain (3.64 x 10(7) um(3)) of Drosophila melanogaster at the nanometer scale with high

82 an electron micrograph dataset for an entire Drosophila melanogaster brain, we reconstruct the first

83 rotective role for neurons and glia in adult Drosophila melanogaster brains.

84 initiation of subcellular lumen formation in Drosophila melanogaster, but not much is known on the wh

85 vision has been extensively characterised in Drosophila melanogaster, but substantially less is known

86 VR has long featured in studies of Drosophila melanogaster, but these experiments have typi

87 ition and organization of the centromeres of Drosophila melanogaster by combining long-read sequencin

88 manipulate the polyandry levels in groups of Drosophila melanogaster by deletion of the female sex pe

89 nonsynonymous mutations in humans, mice, and Drosophila melanogaster by examining patterns of polymor

90 nificantly prevent disease, whereas Smn from Drosophila melanogaster, Caenorhabditis elegans, and Sch

91 The Na(+)/Ca(2+) exchanger of Drosophila melanogaster, CALX, is the main Ca(2+)-extrus

92 the serotonergic system in the vinegar fly, Drosophila melanogaster, can modulate walking speed in a

93 Fruit flies, Drosophila melanogaster, can perform this food-centered

94 of Bruchpilot (Brp), a key component of the Drosophila melanogaster CAZ, participates in SV tetherin

95 uctures of the Schizosaccharomyces pombe and Drosophila melanogaster CENP-C cupin domains at 2.52 and

96 sexually dimorphic aIPg neurons in the adult Drosophila melanogaster central brain whose optogenetic

97 tron microscopy volume, we studied the adult Drosophila melanogaster circuitry associated with antenn

98 predictions, we generated a ClvR element in Drosophila melanogaster ClvR (tko) is located on chromos

99 e real-time dynamics of purified recombinant Drosophila melanogaster CMG unwinding DNA with single-mo

100 Moreover, neuronal overexpression of DCP1 in Drosophila melanogaster confers longevity in adults, whi

101 In Drosophila melanogaster, constitutive co-activation of R

102 Drosophila melanogaster contain a single stac gene, Dsta

103 recent studies using Caenorhabditis elegans, Drosophila melanogaster, Danio rerio, and Mus musculus.

104 expression in a tractable in vivo model, the Drosophila melanogaster developing eye.

105 ats are transcribed in many cells throughout Drosophila melanogaster development, enriched in neurons

106 of Cell, Cassidy et al. (2019) show that, in Drosophila melanogaster, developmental abnormalities res

107 In Drosophila melanogaster, distinct phenotypes have been o

108 nt insights have been provided by studies of Drosophila melanogaster diversifying along the thermal g

109 s study cytokinesis regulators visualized in Drosophila melanogaster (Dm) cells were found to localiz

110 s including broad, cut, and hindsight during Drosophila melanogaster egg chamber development.

111 he T and Tn glycoform O-glycoproteome of the Drosophila melanogaster embryo, and determine that Miner

112 However, in the early Drosophila melanogaster embryo, the heterochromatin lack

113 zation to centrosomes in the rapidly cycling Drosophila melanogaster embryo.

114 , calorimetry, and biochemical assays - that Drosophila melanogaster embryogenesis utilizes 10 mJ of

115 The Drosophila melanogaster embryonic tracheal network is an

116 ping protein-protein interaction networks in Drosophila melanogaster embryos on a system-wide level.

117 ved version of Poly-Ribo-Seq and apply it to Drosophila melanogaster embryos to extend the catalog of

118 q datasets derived from Spiroplasma-infected Drosophila melanogaster embryos, to search for signals o

119 e tracking and microrheology measurements in Drosophila melanogaster embryos.

120 isualize the transcriptional dynamics of the Drosophila melanogaster even-skipped gene at single-cell

121 The fruit fly, Drosophila melanogaster, exhibits consolidated sleep dur

122 Lab-reared Drosophila melanogaster exposed to these same sites also

123 We found that in the vinegar fly, Drosophila melanogaster, exposure to dead conspecifics i

124 In Drosophila melanogaster, exposure to predatory wasps lea

125 s from transgenic Caenorhabditis elegans and Drosophila melanogaster expressing fluorescent proteins.

126 functions demonstrated in isolated brains of Drosophila melanogaster expressing hDAT DeltaN336 and wi

127 Here, we demonstrate that, in Drosophila melanogaster, EYES ABSENT (EYA) acts as a sea

128 sequestering Polo to the microtubules during Drosophila melanogaster female meiosis and suggest that

129 The mating decisions of Drosophila melanogaster females are primarily revealed t

130 Drosophila melanogaster females undergo a variety of pos

131 red an intracellular mechanism that prepares Drosophila melanogaster FGF Branchless (Bnl) for cytonem

132 In Drosophila melanogaster, five different GATA factor gene

133 base editing on the native Atpalpha gene in Drosophila melanogaster flies and retraced the mutationa

134 and courtship behavior were examined of wild Drosophila melanogaster flies isolated from two contrast

135 ion of recombinant Hb-ugt-1 (rHb-ugt-1) into Drosophila melanogaster flies resulted in diminished upr

136 DEET inhibits food ingestion by Drosophila melanogaster flies, and this repellency is me

137 ne the position of 27 sarcomeric proteins in Drosophila melanogaster flight muscles with a quasimolec

138 ess data from 202 fully sequenced hemiclonal Drosophila melanogaster fly lines to perform a genome-wi

139 eep and neural injury responses, we examined Drosophila melanogaster following the removal of antenna

140 lenge the male germline stem cells (GSCs) of Drosophila melanogaster for the production of specialize

141 The Drosophila melanogaster foraging (for) gene is a well-es

142 vo genome assemblies for two wild strains of Drosophila melanogaster from the Drosophila Genetic Refe

143 Here we show that Drosophila melanogaster (fruit fly) subject to obesogeni

144 high-quality, manually curated TE libraries: Drosophila melanogaster (fruit fly), Danio rerio (zebraf

145 PLD blocks ethanol-mediated hyperactivity in Drosophila melanogaster (fruit fly), demonstrating that

146 During Drosophila melanogaster gastrulation, the invagination o

147 gulation using a sequence level model of the Drosophila melanogaster gene even-skipped.

148 In the popular model organism Drosophila melanogaster, gene editing has so far relied

149 m of noncanonical polyadenylation signals in Drosophila melanogaster genes.

150 ments for the sequenced, inbred lines of the Drosophila melanogaster Genetic Reference Panel (DGRP) a

151 of recently collected isofemale lines in the Drosophila melanogaster Genetic Reference Panel (DGRP) c

152 (Entomophthoromycota), in 20 lines from the Drosophila melanogaster Genetic Reference Panel (DGRP).

153 ntified metabolite levels in 40 lines of the Drosophila melanogaster Genetic Reference Panel.

154 se RNA-sequencing of BCBM development with a Drosophila melanogaster genetic screen, and identify Rab

155 ied more than 20,000 euchromatic SVs from 14 Drosophila melanogaster genome assemblies, of which ~40%

156 The Drosophila melanogaster genome has a single locus compri

157 pressor alleles after P-elements invaded the Drosophila melanogaster genome in the mid-twentieth cent

158 s form the second largest gene family in the Drosophila melanogaster genome.

159 hat are flexible enough to be applied to the Drosophila melanogaster genome.

160 In the vinegar fly Drosophila melanogaster, geosmin is decoded in a remarka

161 The fruitfly Drosophila melanogaster has been extensively used as a g

162 Drosophila melanogaster has historically been a workhors

163 Drosophila melanogaster has long been a popular model in

164 ent methods of measuring these parameters in Drosophila melanogaster have low temporal resolution and

165 across the animal kingdom, where studies on Drosophila melanogaster have revealed that sleep phenoty

166 icase family is evolutionarily conserved, as Drosophila melanogaster have three family members: DmBlm

167 t cases of recent selection in the genome of Drosophila melanogaster Here we use a naive population a

168 s that genetically interact with Dube3a, the Drosophila melanogaster homolog of UBE3A.

169 infection model in the genetically amenable Drosophila melanogaster host, in which parasite spores o

170 et al. (2018) demonstrated in the fruit fly Drosophila melanogaster how an enzyme from specific gut

171 ity modulates the courtship behavior of male Drosophila melanogaster in an age-dependent manner.

172 of injured axons, dendrites, and synapses in Drosophila melanogaster In both male and female raw hypo

173 ome manipulation in replicate populations of Drosophila melanogaster in field mesocosms.

174 is decline have been explored intensively in Drosophila melanogaster in recent years and are now star

175 d mutation parameters that are realistic for Drosophila melanogaster In the presence of crossing over

176 d knockdowns in Saccharomyces cerevisiae and Drosophila melanogaster, including carriers, membrane ho

177 In Drosophila melanogaster, individualization of sister spe

178 t cause different reproductive phenotypes in Drosophila melanogaster influence the mRNA transcriptome

179 Drosophila melanogaster instead relies on specialized re

180 mitochondrial protein trafficking pathway in Drosophila melanogaster involving the mitochondria-assoc

181 Drosophila melanogaster is a powerful system for charact

182 Drosophila melanogaster is a unique, powerful genetic mo

183 Drosophila melanogaster is an established model for neur

184 Grooming in Drosophila melanogaster is characterized by repeated exe

185 The fruit fly, Drosophila melanogaster, is well poised as a system in w

186 se patterns, we exposed larvae and adults of Drosophila melanogaster isogenic lines derived from a na

187 l-basal polarity and epithelial integrity in Drosophila melanogaster It is now clear that Scribble ac

188 dy, we used a recently isolated DNA virus of Drosophila melanogaster, Kallithea virus (KV; family Nud

189 We showed previously that the Drosophila melanogaster KDM4A (dKDM4A) histone demethyla

190 transcription factor (bHLH)/PAS proteins in Drosophila melanogaster known as germ cell-expressed (Gc

191 us studies from our laboratory revealed that Drosophila melanogaster lacking RhoGAP18B and Ras Suppre

192 ays to obtain precise optogenetic control in Drosophila melanogaster larvae expressing the light-gate

193 us stimuli, such as parasitoid wasp attacks, Drosophila melanogaster larvae generate a curling and ro

194 rganisms, such as Caenorhabditis elegans and Drosophila melanogaster larvae, to investigate the genet

195 rvate postsynaptic muscles of male or female Drosophila melanogaster larvae.

196 iving tissue is demonstrated in the brain of Drosophila melanogaster larvae.

197 um for cells, Caenorhabditis elegans gonads, Drosophila melanogaster larval brain, mouse retina and b

198 The Drosophila melanogaster larval neuromuscular junction (N

199 on in wild populations of the model organism Drosophila melanogaster Like for most viruses discovered

200 n the alcohol dehydrogenase (ADH) protein of Drosophila melanogaster, like genetic variation in many

201 To address this question, we analyze Drosophila melanogaster lines harboring a deletion withi

202 the dosage of fission and fusion genes in a Drosophila melanogaster loss-of-function model and found

203 Here we show that T-antigen in Drosophila melanogaster macrophages is involved in their

204 de in vivo map of miRNA-mRNA interactions in Drosophila melanogaster, making use of single nucleotide

205 otyped sequence of engagement actions during Drosophila melanogaster male courtship behavior.

206 3, histone H4 is inherited asymmetrically in Drosophila melanogaster male germline stem cells undergo

207 ith fluorescent sperm labeling, we show that Drosophila melanogaster males exercise independent contr

208 During courtship, Drosophila melanogaster males pattern their songs using

209 Drosophila melanogaster males perform a series of courts

210 ntercellular attachments in epithelia during Drosophila melanogaster mesoderm invagination.

211 ic alterations in the brains of an inducible Drosophila melanogaster model of AD expressing the Arcti

212 We utilized a Drosophila melanogaster model system to assess the effec

213 We used the Drosophila melanogaster model to characterize metabolic

214 nteric diseases, we report on the use of the Drosophila melanogaster model to identify a novel functi

215 Here, we use the Drosophila melanogaster model to reveal a pivotal role f

216 We have developed a Drosophila melanogaster model to study the molecular eff

217 Drosophila melanogaster models of skeletal muscle lamino

218 l dysfunction, in Caenorhabditis elegans and Drosophila melanogaster models of WS.

219 In Drosophila melanogaster, most sexually dimorphic traits

220 In Drosophila melanogaster, most SFPs are produced in the a

221 n neural stem cells and its association with Drosophila melanogaster motility behavior.

222 In Drosophila melanogaster motor neurons, activation of Rab

223 Homologous LARKs from Bombyx mori, Drosophila melanogaster, Mus musculus and Homo sapiens b

224 arse olfactory inputs to Kenyon cells of the Drosophila melanogaster mushroom body.

225 At the embryonic neuromuscular junction of Drosophila melanogaster, mutation or knockdown of many k

226 The EXO domain of A. aegypti and Drosophila melanogaster Nbr adopt a mixed alpha/beta-sca

227 The kinesin-14 motor proteins (Drosophila melanogaster Ncd, Saccharomyces cerevisiae Ka

228 In Drosophila melanogaster, NF-kappaB signaling-mediated im

229 es but has also reportedly inserted into the Drosophila melanogaster nuclear export factor gene nxf2.

230 dy the neuronal circuitry that allows larval Drosophila melanogaster of either sex to negotiate this

231 documented the presence of the fruit fly or Drosophila melanogaster on alcohol-containing food sourc

232 tsetse fly antenna and that of the fruit fly Drosophila melanogaster One morphological type of sensil

233 ) resolution X-ray structural information on Drosophila melanogaster Orai in an open conformation (Ho

234 In Drosophila melanogaster, OSNs expressing specific recept

235 ene sets associated with development rate in Drosophila melanogaster Our transcriptional data also su

236 The protein Ebony from Drosophila melanogaster plays a central role in the regu

237 se deep genomic population sequencing of two Drosophila melanogaster populations to measure selection

238 uppression tactics have been well studied in Drosophila melanogaster, primarily during RNA, but not D

239 study the hydrophobic membrane motifs of two Drosophila melanogaster proteins, GPAT4 and ALG14, that

240 In Drosophila melanogaster, proteins in the seminal fluid a

241 re, we make the unexpected discovery that in Drosophila melanogaster PTEN reduces PtdIns(4,5)P(2) lev

242 While activation of myosin II in Drosophila melanogaster pupal retina leads to increased

243 In Drosophila melanogaster, recently discovered synapse-lev

244 In the male germline of Drosophila melanogaster repression of Stellate genes by

245 n during early nervous system development in Drosophila melanogaster requires precise regulation of g

246 in plant (Arabidopsis thaliana) and animal (Drosophila melanogaster) research.

247 SCAF4 ortholog CG4266 in the model organism Drosophila melanogaster resulted in impaired locomotor f

248 e-based RNA interference screen using stable Drosophila melanogaster S2 cells expressing the enhanced

249 In Drosophila melanogaster, SDs are present in nephrocytes,

250 We show here that the Drosophila melanogaster SETD1A orthologue is required in

251 In Drosophila melanogaster, SGP-derived Hedgehog (Hh), whic

252 Syntenic analysis of Glossina relative to Drosophila melanogaster shows reduced structural conserv

253 Previously, we found that Drosophila melanogaster SNAPc (DmSNAPc) bound to the U6

254 um falciparum microgametocytes and human and Drosophila melanogaster sperm), very little is known abo

255 The mushroom body neurons (MBn) in Drosophila melanogaster store protein synthesis-dependen

256 ed in a population of fully sequenced inbred Drosophila melanogaster strains when flies developed in

257 We have sequenced the genomes of Drosophila melanogaster strains with exceptional longevi

258 e alphaPS3 integrin, scab) in the fruit fly (Drosophila melanogaster) suggests that gastrulation in t

259 ically manipulated the social environment of Drosophila melanogaster, testing individual flies and dy

260 more likely to encode essential functions in Drosophila melanogaster than ancient, conserved ZAD-ZNF

261 Here we review recent evidence from Drosophila melanogaster that microbial cues recruit anti

262 Here, we present a homing drive in Drosophila melanogaster that reduces the prevalence of r

263 wo genetically modified invertebrate models (Drosophila melanogaster) that develop invasive or non-in

264 of the two evolutionarily conserved genes in Drosophila melanogaster, the authors found that their kn

265 In Drosophila melanogaster, the distribution of CS on the e

266 In Drosophila melanogaster, the prothoracicotropic hormone

267 In Drosophila melanogaster, the striking daily structural r

268 In this study, a transcriptomic analysis in Drosophila melanogaster third instar larvae was carried

269 xpression of human EZHIP reduces H3K27me3 in Drosophila melanogaster through a conserved mechanism.

270 ine neuron loss and locomotor dysfunction in Drosophila melanogaster through an aberrant increase in

271 We have examined the response of Drosophila melanogaster to acetic acid, a tastant that c

272 lbut virus, is common in wild populations of Drosophila melanogaster To begin to understand the proce

273 ) neurons in the optic lobe of the fruit fly Drosophila melanogaster to characterize divergent proper

274 Here, we use the model organism Drosophila melanogaster to delineate how KDM5 contribute

275 used the pregrastrula-patterning network of Drosophila melanogaster to demonstrate that loss in accu

276 Here we use a genetic screen in Drosophila melanogaster to identify Hodor, an ionotropic

277 When we exposed populations of Drosophila melanogaster to intense parasitism by the par

278 Here, we use the intestine of Drosophila melanogaster to investigate how gut-derived s

279 Here, we used adults of the fruit fly Drosophila melanogaster to investigate the metabolic cha

280 In a screen for neurons that enable Drosophila melanogaster to retreat when it encounters a

281 e developed a novel experimental paradigm in Drosophila melanogaster to study the mechanisms underlyi

282 In this study, we used the fruit fly, Drosophila melanogaster, to investigate how infection th

283 Knockdowns were induced in hNPCs and Drosophila melanogaster using RNA interference.

284 rolled by SIN3 and SAM synthetase (SAM-S) in Drosophila melanogaster Using several approaches, includ

285 ection conferred by Spiroplasma to its host, Drosophila melanogaster varies with strain of attacking

286 that Chlamydomonas VIG1, an ortholog of the Drosophila melanogaster Vasa intronic gene (VIG), is req

287 ells and for mapping of neuronal activity in Drosophila melanogaster via genetically encoded Ca(2+) i

288 Using Drosophila melanogaster, we created the first animal mod

289 xamining the diversity of enteric neurons in Drosophila melanogaster, we identify a key role for gut-

290 of P-element derived transgene insertions in Drosophila melanogaster, we show here that raising flies

291 In Drosophila melanogaster, we show that 4 genes of the maj

292 Here, using genetic techniques possible in Drosophila melanogaster, we tested the hypothesis that v

293 Or22a, and Or71a from the common fruit fly, Drosophila melanogaster, were recombinantly expressed, p

294 onal immediate early gene; and 3) in vivo in Drosophila melanogaster, where developmental exposures t

295 se body size is larger than the model insect Drosophila melanogaster, which enabled us to more easily

296 in vivo, we studied the unique Rh50 gene of Drosophila melanogaster, which encodes two isoforms, Rh5

297 recently published structure of spastin from Drosophila melanogaster, which forms a six-subunit spira

298 rformed targeted assays on selected genes in Drosophila melanogaster, which we suspected of being inv

299 exit during terminal differentiation in the Drosophila melanogaster wing.

300 of Drosophila simulans, a close relative of Drosophila melanogaster with which it co-occurs on both