ライフサイエンスコーパス: Drosophila melanogaster

1 ents ROO, GYPSY and DM412 on a chromosome of Drosophila melanogaster .

2 expanded to include an extra model organism (Drosophila melanogaster).

3 we expressed the human DISC1 in fruit flies (Drosophila melanogaster).

4 of host lipid stores in the model arthropod Drosophila melanogaster.

5 ersus strictly cell-autonomous mechanisms in Drosophila melanogaster.

6 ostasis in the gut of both Aedes aegypti and Drosophila melanogaster.

7 ia alters the social communication system of Drosophila melanogaster.

8 g cardiac function in intact, unanesthetized Drosophila melanogaster.

9 r neurons (GRNs) in tarsal taste sensilla of Drosophila melanogaster.

10 rtion of strongly deleterious mutations than Drosophila melanogaster.

11 profiles for protein function prediction in Drosophila melanogaster.

12 t are modulated upon mating in the fruit fly Drosophila melanogaster.

13 fluence aggressive behavior of the fruit fly Drosophila melanogaster.

14 essary for hygrosensation in the vinegar fly Drosophila melanogaster.

15 c, pharmacological and optical approaches in Drosophila melanogaster.

16 s has increasingly included the vinegar fly, Drosophila melanogaster.

17 tochromes from Chlamydomonas reinhardtii and Drosophila melanogaster.

18 rrelation method on the experimental data of Drosophila melanogaster.

19 ion and exploration decisions taken by adult Drosophila melanogaster.

20 SAGA) transcriptional coactivator complex in Drosophila melanogaster.

21 the uptake of an AsHC in the model organism Drosophila melanogaster.

22 the neuronal phenotype of EPG5 knock-down in Drosophila melanogaster.

23 f dead neurons in the brain of the fruit fly Drosophila melanogaster.

24 ents with any sexually-reproducing metazoan, Drosophila melanogaster.

25 could identify circadian output circuits in Drosophila melanogaster.

26 the maternal inheritance of mitochondria in Drosophila melanogaster.

27 ulation of apoptotic neurons in the brain of Drosophila melanogaster.

28 ences of size increase in highland Ethiopian Drosophila melanogaster.

29 ia abdita, but only one, the amnioserosa, in Drosophila melanogaster.

30 domain-containing nuclear reader protein in Drosophila melanogaster.

31 ian transcriptomes in heads of young and old Drosophila melanogaster.

32 opulations of visually responsive neurons in Drosophila melanogaster.

33 our in many species, including the fruit fly Drosophila melanogaster.

34 rity with the ELO of Tribolium castaneum and Drosophila melanogaster.

35 ionotropic receptor have been identified in Drosophila melanogaster.

36 ogical processes and developmental stages of Drosophila melanogaster.

37 of the naturally occurring engrailed-HD from Drosophila melanogaster.

38 odimers that induce prophylactic immunity in Drosophila melanogaster.

39 ts of piRNA biogenesis have been revealed in Drosophila melanogaster.

40 tive of resistance to bacterial infection in Drosophila melanogaster [13].

41 flanked gRNAs to induce mutations in vivo in Drosophila melanogaster - a strategy that could readily

42 In the male germline of Drosophila melanogaster, a novel but poorly understood f

43 In Drosophila melanogaster, a single G protein-coupled rece

44 cell behavior in the female germline cyst in Drosophila melanogaster, a stereotypically wired network

45 Among these is the common fruit fly Drosophila melanogaster, a well-established model organi

46 In Drosophila melanogaster, a widely-used technique for ref

47 In exploring how Drosophila melanogaster acquires its microbiome, we foun

48 Here, we report that Drosophila melanogaster adult flies exhibit a kicking re

49 The pattern of the Drosophila melanogaster adult wing is heavily influenced

50 Herein, we provide evidence that Drosophila melanogaster AgmNAT (CG15766) catalyzes the f

51 highly reminiscent of that of the fruit fly, Drosophila melanogaster Altogether, our work unveils the

52 Using Drosophila melanogaster and an array of viruses that inf

53 ompared to state of the art approaches using Drosophila melanogaster and Arabidopsis thaliana data.

54 The method has been applied to human, mouse, Drosophila melanogaster and Caenorhabditis elegans cells

55 lyses of the homologs of RBPJ and L3MBTL3 in Drosophila melanogaster and Caenorhabditis elegans demon

56 that mutation of the SLC13A5 orthologues in Drosophila melanogaster and Caenorhabditis elegans promo

57 scription pattern, the invertebrate pattern (Drosophila melanogaster and Caenorhabditis elegans) prof

58 odel species, most notably mouse, zebrafish, Drosophila melanogaster and Caenorhabditis elegans.

59 We studied Drosophila melanogaster and compared the relative contri

60 Hybrids between Drosophila melanogaster and Drosophila simulans are ster

61 cted based on sequences from a model species Drosophila melanogaster and four aphid species Acyrthosi

62 and defeats in dyadic pairings between male Drosophila melanogaster and how long those effects remai

63 ction that differ among natural genotypes of Drosophila melanogaster and investigate their consequenc

64 he cellular toxicity of sulfide, and rescued Drosophila melanogaster and mice from lethal exposures o

65 hyltransferase family, which includes Trr in Drosophila melanogaster and MLL3 (encoded by KMT2C) and

66 and associated with cardiac abnormalities in Drosophila melanogaster and Mus musculus.

67 olbachia pipientis genomic DNA from infected Drosophila melanogaster and Mycobacterium tuberculosis f

68 In Drosophila melanogaster and other animals, primordial ge

69 We used Drosophila melanogaster and Saccharomyces cerevisiae to

70 organisms, including Caenorhabditis elegans, Drosophila melanogaster, and mice, but have a negligible

71 ion of inhibitory local neurons (LNs) in the Drosophila melanogaster antennal lobe, the analog of the

72 d, and it is unclear whether animals such as Drosophila melanogaster are endowed with this sense.

73 rated that molecular clocks in the fruit fly Drosophila melanogaster are regulated differently in clo

74 proximal centriole-like structure [PCL]) in Drosophila melanogaster are remodeled during spermiogene

75 previously estimated bottlenecks for African Drosophila melanogaster are too extreme.

76 ng age-dependent decline in phototaxis using Drosophila melanogaster as a genetic model system.

77 The results develop Drosophila melanogaster as a model for sex-specific stre

78 n cells, we then evaluated the effects using Drosophila melanogaster as an in vivo model.

79 tative cofactors/collaborators analysis (for Drosophila melanogaster), as they are crucial for the in

80 eted high-throughput metabolite profiling in Drosophila melanogaster at different ages, we demonstrat

81 In the fruit fly, Drosophila melanogaster, aversive olfactory learning for

82 oporins (ClGlp1 and ClGlp2) and a homolog of Drosophila melanogaster big brain (ClBib).

83 d for mesoderm invagination in the fruit fly Drosophila melanogaster but do not appear during mesoder

84 a was lethal to closely related fruit flies (Drosophila melanogaster) but induced no adverse effects

85 d adult phenotypes and social composition in Drosophila melanogaster - by experimentally manipulating

86 on of mitochondria in mouse and fruit flies (Drosophila melanogaster) by electron cryo-tomography and

87 DNA haplotype into replicated populations of Drosophila melanogaster causes numerical population supp

88 Here, we show that in Drosophila melanogaster Cdk5 regulates basal autophagy,

89 Here, we show that in the Drosophila melanogaster cell wound repair model Rho GTPa

90 kac show that actomyosin ring closure during Drosophila melanogaster cellularization uses two steps,

91 tly discovered in a neural population in the Drosophila melanogaster central complex, a brain region

92 cou and Hall" courtship song rhythms of male Drosophila melanogaster, claiming that these ultradian a

93 he recent resolution of dDAT structures from Drosophila melanogaster, complete understanding of its m

94 SKI-1/S1P of arthropods, like the fruit fly Drosophila melanogaster, contains a shorter prodomain co

95 and T4lec, had a clear activating effect on Drosophila melanogaster core 1 galactosyltransferase enz

96 xpression in transgenic, uninfected males of Drosophila melanogaster crossed to uninfected females ca

97 Drosophila melanogaster CRYPTOCHROME (CRY) mediates beha

98 photo-induced electron transfer reactions in Drosophila melanogaster cryptochrome are indeed influenc

99 Here we identify a region of the Drosophila melanogaster CTD that is essential for Pol II

100 We examined the Drosophila melanogaster (d) mutant dDAT-G108Q, which lea

101 s) from eight species (Arabidopsis thaliana, Drosophila melanogaster, Danio rerio, Homo sapiens, Mus

102 In Drosophila melanogaster, DAT deficiency results in reduc

103 In the peripheral nervous system of Drosophila melanogaster, differential Notch signaling be

104 Here we show that Drosophila melanogaster display strong aversive response

105 lasses of taste projection neurons (TPNs) in Drosophila melanogaster distinguished by their morpholog

106 cloned from Balanus improvisus (BiOctR) and Drosophila melanogaster (DmOctR), little is known about

107 onstructed SERT homology models based on the Drosophila melanogaster dopamine transporter and docked

108 ave been shown to bind to cholesterol/CHS in Drosophila melanogaster dopamine transporter.

109 the temperature preference of the fruit fly, Drosophila melanogaster, during infection with the funga

110 ons driving collective cell migration during Drosophila melanogaster egg morphogenesis through its in

111 Neural stem cells or neuroblasts in the Drosophila melanogaster embryo delaminate as single cell

112 enylated transcripts within the first 2 h of Drosophila melanogaster embryogenesis.

113 As a case study we choose Drosophila melanogaster embryonic cells, for which both

114 ntire developing zebrafish (Danio rerio) and Drosophila melanogaster embryos and perform adaptive who

115 orm in vivo single-molecule imaging in early Drosophila melanogaster embryos of the transcription fac

116 e imaging of ingressing neuroblasts (NBs) in Drosophila melanogaster embryos to assess apical domain

117 During cleavage in Drosophila melanogaster embryos, actomyosin rings constr

118 ion of CME dynamics during dorsal closure of Drosophila melanogaster embryos.

119 pression along the dorsoventral (DV) axis of Drosophila melanogaster embryos.

120 eolar proteins assemble into the nucleoli of Drosophila melanogaster embryos.

121 As the fruit fly Drosophila melanogaster expresses Tau proteins (dTau) th

122 Here, we report that Drosophila melanogaster females but not males adapt to h

123 We use both methods in Drosophila melanogaster, first generating our own novel

124 mental (short- and longer-term) evolution in Drosophila melanogaster Flies with autonomous and nonaut

125 ependence of synaptic vesicle endocytosis in Drosophila melanogaster Flower is predominantly localize

126 ing on the most extensively studied species, Drosophila melanogaster, FlyBase includes information on

127 We found that Drosophila melanogaster Fmr1 mutants exhibit increased s

128 Drosophila melanogaster, for example, generally initiate

129 In Drosophila melanogaster, for instance, male fertility in

130 In vivo studies in Drosophila melanogaster found that loss of either compon

131 Here we study Drosophila melanogaster from 'Evolution Canyon' in Israe

132 sed assays with spatiotemporal resolution in Drosophila melanogaster (fruit fly) and Danio rerio (zeb

133 The Drosophila melanogaster (fruit fly) gene Diap1 encodes a

134 Using an integrative approach that combines Drosophila melanogaster (fruit fly) genetics with transc

135 itions (EMTs), loss of adherens junctions in Drosophila melanogaster gastrula is delayed until mesode

136 nctional disassembly and postpone EMT during Drosophila melanogaster gastrulation.

137 nt time, viability and adult activity in the Drosophila melanogaster Genetic Reference Panel (DGRP) a

138 of age in the sequenced, inbred lines of the Drosophila melanogaster Genetic Reference Panel (DGRP) a

139 the unrelated, sequenced inbred lines of the Drosophila melanogaster Genetic Reference Panel.

140 the unrelated, sequenced inbred lines of the Drosophila melanogaster Genetic Reference Panel.

141 their homologs are an essential part of the Drosophila melanogaster genetic toolkit.

142 pilation of over 1100 worldwide wild-derived Drosophila melanogaster genome sequences reassembled usi

143 Here, we utilized the ability of Drosophila melanogaster germline stem cells (GSCs) to su

144 olution and intravital imaging of developing Drosophila melanogaster glutamatergic synapses revealed

145 Here, we have characterized a Drosophila melanogaster glutathione transferase (DmGSTE6

146 of bacterial colonization in the fruit fly (Drosophila melanogaster) gut.

147 The fruit fly Drosophila melanogaster has become a valuable experiment

148 The model organism Drosophila melanogaster has been at the forefront of gen

149 The 91-R strain of Drosophila melanogaster has been intensely selected with

150 microbiome in determining this type of RI in Drosophila melanogaster has been proposed.

151 nes, and experimentally imposing monogamy on Drosophila melanogaster has led to a relative feminisati

152 the invertebrates Caenorhabditis elegans and Drosophila melanogaster has led to new insights into the

153 Drosophila melanogaster has one of best-described transc

154 The fruit fly Drosophila melanogaster has only one histone H2A variant

155 The foraging gene in Drosophila melanogaster has previously been implicated i

156 this end, FlyBase (flybase.org), the MOD for Drosophila melanogaster, has established a 'Gene Group'

157 Research using the fruit fly, Drosophila melanogaster, has helped us understand the ge

158 te TRAPP function in metazoans, we show that Drosophila melanogaster have two TRAPP complexes similar

159 gy to study the impact of temperature on the Drosophila melanogaster head transcriptome.

160 y in different tissues and cultured cells of Drosophila melanogaster, highlighting their contribution

161 Hrb98DE and mrj are the Drosophila melanogaster homologs of human hnRNPA2B1 and

162 tin organization and regulation, we purified Drosophila melanogaster HP1a interactors, and performed

163 Here, we used Drosophila melanogaster, in conjunction with the biosafe

164 The gut of Drosophila melanogaster includes a proximal acidic regio

165 ct insecticidal activity toward fruit flies (Drosophila melanogaster) indicates that Form II is more

166 Using Drosophila melanogaster indirect flight muscle S1, we pe

167 Here we use the Drosophila melanogaster intestine to investigate the nat

168 Drosophila melanogaster is a natural host of parasitic w

169 Drosophila melanogaster is a well suited model system wi

170 The fruit fly Drosophila melanogaster is a widely used model for cell

171 The fruit fly Drosophila melanogaster is an excellent model for deciph

172 Aging in Drosophila melanogaster is characterized by loss of repr

173 nce that a polymorphism in an enzyme gene in Drosophila melanogaster is maintained by such a trade-of

174 Drosophila melanogaster is the paradigm for insect devel

175 ternative, broad spectrum methyltransferase, Drosophila melanogaster Juvenile Hormone Acid O-Methyltr

176 fetime imaging to interact directly with the Drosophila melanogaster kinesin-1 light chain (KLC) tetr

177 to analyze the behavior and conformation of Drosophila melanogaster kinesin-13 KLP10A protein constr

178 noscopy of sub-cellular structures of intact Drosophila melanogaster larvae and of resected tissues.

179 ate how food-search behavior is organized in Drosophila melanogaster larvae dwelling in hydrogels mim

180 tential for purging using inbred and outbred Drosophila melanogaster larvae exposed to biotic (larval

181 Drosophila melanogaster larvae irradiated with doses of

182 Like most animals, Drosophila melanogaster larvae respond to a variety of n

183 Drosophila melanogaster larvae whose primary nociceptive

184 In Drosophila melanogaster larvae, the prime site of extern

185 both heterochromatic and euchromatic loci in Drosophila melanogaster Live imaging of single DSBs in l

186 The Drosophila melanogaster male courtship song provides a p

187 Drosophila melanogaster males have one X chromosome, whe

188 During courtship, Drosophila melanogaster males sing to females a song com

189 Drosophila melanogaster males with a reduction in dMBD-R

190 We show that, in Drosophila melanogaster males, sleep pressure after slee

191 e we demonstrate, using a well characterized Drosophila melanogaster malignant tumour model, that non

192 In Drosophila melanogaster, many SC components and their ge

193 In the fruit fly, Drosophila melanogaster, mating and the receipt of male

194 Here, we show that the abundant Drosophila melanogaster microRNA mir-276a regulates mole

195 We show that in Drosophila melanogaster, mild TZ defects are observed in

196 of systemic immune cells is compromised in a Drosophila melanogaster model of Fragile X, highlighting

197 The present study used the Drosophila melanogaster model system and a candidate gen

198 ry neurons and reduced the survival of novel Drosophila melanogaster models of SCA35.

199 that meiotic crossover patterning is lost in Drosophila melanogaster mutants that lack the Bloom synd

200 the E3 ubiquitin ligase Neuralized (Neur) in Drosophila melanogaster Neur interacts with and down-reg

201 for cell polarity in asymmetrically dividing Drosophila melanogaster neuroblasts (NBs; neural stem ce

202 f acentric chromosome fragments generated in Drosophila melanogaster neuroblasts.

203 c and pharmacological intervention in larval Drosophila melanogaster of both sexes to address localiz

204 Courtship in Drosophila melanogaster offers a powerful experimental p

205 on that coordinate the sensory identities of Drosophila melanogaster olfactory receptor neurons (ORNs

206 In Drosophila melanogaster olfactory sensory neurons (OSNs)

207 t originally developed to describe fruitfly (Drosophila melanogaster) olfactory association, can also

208 During Drosophila melanogaster oogenesis, spindle assembly occu

209 Surprisingly, unlike in Drosophila melanogaster, orco mutant ants also lack most

210 f the centriole protein Asterless (Asl), the Drosophila melanogaster orthologue of Cep152, prevents c

211 brane and is required for the development of Drosophila melanogaster ovarian follicles and NE morphol

212 We report that in the development of the Drosophila melanogaster ovary, the Hedgehog (Hh) gradien

213 d/truncated TDP-43 was observed for HSPB8 in Drosophila melanogaster Overexpression of HSP67Bc, the f

214 to identify the substrate specificity of the Drosophila melanogaster P-TEFb (DmP-TEFb) in vitro.

215 s a contig NG50 of >21 Mbp on both human and Drosophila melanogaster PacBio data sets.

216 In the fruit fly, Drosophila melanogaster, Pax6 also functions in a range

217 observe that binary cell fate choice in the Drosophila melanogaster peripheral sensory organ lineage

218 In the fruit fly, Drosophila melanogaster, photoreceptors R7 and R8 in the

219 The Drosophila melanogaster Piwi protein regulates both nich

220 rica and Eurasia, hundreds of genomes from a Drosophila melanogaster population in Africa, and tens o

221 chemically similar sugars-L- and D-arabinose-Drosophila melanogaster prefers D- over L- arabinose, bu

222 we show that akin to mammals, the fruit fly, Drosophila melanogaster, prefers food with a specific ha

223 Drosophila melanogaster presents an advantageous model s

224 Drosophila melanogaster presents an advantageous model t

225 ary origins of these cues and report that in Drosophila melanogaster pro- and mature neurotrophins ar

226 trates of reward perception in the fruit fly Drosophila melanogaster prompted us to develop a simpler

227 lls (ISCs) maintain the midgut epithelium in Drosophila melanogaster Proper cellular turnover and tis

228 ssifier-based function prediction method for Drosophila melanogaster proteins, FFPred-fly+.

229 e, in conjunction with the platinum standard Drosophila melanogaster reference genome, we analyze rec

230 Coalescence of the embryonic gonad in Drosophila melanogaster requires directed migration of p

231 ma subunit (LanB2) in the peripheral glia of Drosophila melanogaster results in the disruption of gli

232 emonstrate that mate choice in the fruit fly Drosophila melanogaster results in the linear sorting of

233 blasts, while global knockdown of the single Drosophila melanogaster riboflavin transporter homologue

234 (Ago2) is a rapidly evolving nuclease in the Drosophila melanogaster RNA interference (RNAi) pathway

235 of the RHD domains of MsDorsal and MsRel2 in Drosophila melanogaster S2 and Spodoptera frugiperda Sf9

236 CrPV(R146A) virus infection is attenuated in Drosophila melanogaster S2 cells and adult fruit flies a

237 of cross-linking MT plus ends and F-actin in Drosophila melanogaster S2 cells to gain insight into sp

238 Drosophila melanogaster sarcomere length short (SALS) is

239 The Drosophila melanogaster scaffolding protein Stardust (Sd

240 pliant platform called ExpreS(2), based on a Drosophila melanogaster Schneider 2 (S2) stable cell lin

241 The fruitfly Drosophila melanogaster senses day-night cycles in part

242 NA-Seq data sets from four samples of larval Drosophila melanogaster sensory neurons, and used three

243 ) utilizes low-affinity binding sites in the Drosophila melanogaster shavenbaby (svb) locus and relat

244 A study in the fruit fly Drosophila melanogaster shows that satellite DNA, and co

245 ed the first new reference-quality genome of Drosophila melanogaster since its initial sequencing.

246 ral differences between the rover and sitter Drosophila melanogaster strains, but the molecular mecha

247 genes of the dosage compensation pathway of Drosophila melanogaster suppressed male killing caused b

248 mically and genetically interact, modulating Drosophila melanogaster synapse morphology and homeostat

249 In the Malpighian (renal) tubule of Drosophila melanogaster, TA activates a transepithelial

250 gene transfer rate is significantly lower in Drosophila melanogaster than in the Drosophila simulans

251 dentities of neurons in the antennal lobe of Drosophila melanogaster that express each of the recepto

252 enylation element-binding protein homolog in Drosophila melanogaster that forms functional amyloids n

253 To do so, we used long-lived female Drosophila melanogaster that had their insulin signallin

254 tabolic genes from eastern US collections of Drosophila melanogaster that span a large latitudinal ra

255 In Drosophila melanogaster the daily locomotion patterns of

256 regulation: the segment polarity network in Drosophila melanogaster, the cell cycle of budding yeast

257 In Drosophila melanogaster, the sex pheromone produced by m

258 In Drosophila melanogaster third instar larvae expressing C

259 herichia coli, Saccharomyces cerevisiae, and Drosophila melanogaster This simple, yet effective techn

260 researchers have made remarkable progress in Drosophila melanogaster to address how a myriad of conte

261 s, we expressed Abeta36-40 and Abeta42-43 in Drosophila melanogaster to evaluate inherent toxicity an

262 Here, we have used Drosophila melanogaster to explore the contribution of i

263 petition by introducing a second genome into Drosophila melanogaster to follow transmission.

264 Our goal was to use Drosophila melanogaster to identify evolutionarily conse

265 hanical disruption and genetic approaches in Drosophila melanogaster to identify hearing as an import

266 Here, we use Drosophila melanogaster to model this mutation and disse

267 Here we exposed populations of Drosophila melanogaster to repeated seasonal changes in

268 Here, we use Drosophila melanogaster to study whether neprilysins are

269 s that are expressed in the adult fruit fly, Drosophila melanogaster: TpnC4 is predominantly expresse

270 Administration of actin to Drosophila melanogaster triggers a response characterise

271 The retinas of Drosophila melanogaster use just two main types, in whic

272 rates of locomotion and social behaviors for Drosophila melanogaster using automated machine-vision a

273 sposon insertions in neurons from individual Drosophila melanogaster using whole-genome sequencing.

274 We report that, in Drosophila melanogaster, variation in ambient temperatur

275 e maturation and proper lysosome function in Drosophila melanogaster We demonstrate that Rab2 binds t

276 e Drosophila C virus (DCV) in populations of Drosophila melanogaster We found extensive allelic heter

277 ying the model to Caenorhabditis elegans and Drosophila melanogaster, we achieved satisfactory result

278 the dynamics of ingestion in the vinegar fly Drosophila melanogaster, we developed Expresso, an autom

279 he well-characterized chemosensory system of Drosophila melanogaster, we have analysed genome-wide da

280 Using the fruit fly Drosophila melanogaster, we identified neurons in the br

281 upled with homology-directed repair (HDR) in Drosophila melanogaster, we introduced both substitution

282 To explore principles of TAD folding in Drosophila melanogaster, we performed Hi-C and poly(A)(+

283 are observed in dividing epithelial cells in Drosophila melanogaster, we propose that cell-cycle-coup

284 ions in ancestral orthologs of both genes in Drosophila melanogaster were associated with altered sen

285 This model is consistent with findings in Drosophila melanogaster, where gap genes were found to b

286 rthropods is best understood in the ovary of Drosophila melanogaster, where it acts to silence active

287 Here we report that ETH persists in adult Drosophila melanogaster, where it functions as an obliga

288 This mechanism is found in the fruit fly Drosophila melanogaster, where polyploid ovarian follicl

289 the formation of alternate body segments in Drosophila melanogaster Whereas Drosophila embryos are l

290 pathogenic mutations in ATP7 proteins using Drosophila melanogaster, which has a single orthologue o

291 m/solute co-transporter-like-(or cupcake) in Drosophila melanogaster, which is required for the fly t

292 In the fruit fly Drosophila melanogaster, which shows a robust diurnal pa

293 n of the structure of the full length CTD of Drosophila melanogaster, which we conclude is a compact

294 We used Drosophila melanogaster wing vein and scutellar bristle

295 nknown function for recurved bristles on the Drosophila melanogaster wing.

296 atasets and present results on datasets from Drosophila melanogaster wings and Schmidtae mediterranea

297 l experimental system in which we challenged Drosophila melanogaster with the pathogen Listeria monoc

298 f all major autosomal complex satDNA loci in Drosophila melanogaster, with a particular focus on the

299 e investigated the pentameric TOG array of a Drosophila melanogaster XMAP215 member, Msps.

300 26 transformation-specific family repressors Drosophila melanogaster Yan and its human homolog TEL/ET