ライフサイエンスコーパス: Drosophila

1 incorporate work on more insect taxa beyond Drosophila.

2 regulation of TSC dynamics in HeLa cells and Drosophila.

3 utes to cognition and synaptic morphology in Drosophila.

4 lls of several species, including humans and Drosophila.

5 domeless, to activate JAK/STAT signalling in Drosophila.

6 anscriptomic diversity of the optic lobes of Drosophila.

7 ecifies and maintains hematopoietic sites in Drosophila.

8 isms of an object-selective neuron, LC11, in Drosophila.

9 re key regulators of sleep in mammals and in Drosophila.

10 is critical for miRNA function in plants and Drosophila.

11 teractions between Sting and Pink1/parkin in Drosophila.

12 s and embryos, human biopsies, organoids and Drosophila.

13 l chondroitin sulfate proteoglycan (CSPG) in Drosophila.

14 o involved in suppressing sex ratio drive in Drosophila.

15 ate, fertility and neurological functions in Drosophila.

16 c AL reductions in ants [13, 14], but not in Drosophila [15].

17 acterized a head-specific approach to TBI in Drosophila, a powerful genetic system that shares many c

18 In Drosophila, activation of the dorsal fan-shaped body (dF

19 We generated a Drosophila Adar(E374A) mutant strain encoding a catalyti

20 to innate immune induction, indicating that Drosophila Adar, despite being the homolog of mammalian

21 d kinase Gilgamesh (Gish)/CK1gamma maintains Drosophila adult midgut homeostasis by restricting JNK p

22 We carried out in vivo time-lapse imaging of Drosophila adult sensory neuron differentiation, integra

23 oactive peptide (CCAP)-expressing neurons in Drosophila adults regulate feeding behavior and metaboli

24 Together, our data show that Drosophila AGO1 functions outside of the RISC to repress

25 ons, from either mouse or human patients, in Drosophila allowing intricate analysis of the PCP pathwa

26 Here, we use Drosophila, an established model for studies on triglyce

27 development in ants reveals that - unlike in Drosophila and as in mammals - olfactory receptors may p

28 ed intracellular Ca(2+) and neurotoxicity in Drosophila and cultured primary mouse neurons.

29 ivity throughout the entire central brain of Drosophila and make comparisons across trials, individua

30 olded proteins were found to be conserved in Drosophila and mammalian cells.

31 tained from oocytes to fertilized embryos in Drosophila and mammals.

32 Using Drosophila and mouse embryonic stem cells, we characteri

33 ck-in human dopaminergic SH-SY5Y cell lines, Drosophila and mouse models.

34 ctivity of presynaptic ENaC channels in both Drosophila and mouse.

35 ion of mushroom body lobes that, as shown in Drosophila and other hexapods, contain networks essentia

36 ized that the longer FGF proteins present in Drosophila and other organisms may relate to an ancestra

37 levels in patient-derived fibroblasts and in Drosophila, and also dramatically ameliorated motor and

38 ndings from metabolomics studies using mice, Drosophila, and zebrafish.

39 he intertwined socket and shaft cells of the Drosophila anterior wing margin mechanosensory bristles

40 tical in vivo recordings from freely walking Drosophila are currently possible only for limited behav

41 ort novel tumour suppressor activity for the Drosophila Argonaute family RNA-binding protein AGO1, a

42 derpinnings were first carried out utilizing Drosophila as a model system.

43 of the fly leg motor system and establishes Drosophila as a tractable system for investigating neura

44 Using the fruit fly Drosophila as an example, we discuss recent work that ha

45 subunit serves as a cofactor of GATA TFs in Drosophila, as shown in mammals.

46 Using the Drosophila border cell migration model, we find that Pro

47 To address this, we use Drosophila border cell migration, an invasive, collectiv

48 Here, we establish the Drosophila border cells as a model for this multistep pr

49 Here, we used Drosophila border cells, an established model for in viv

50 The Drosophila brain contains a relatively simple circuit fo

51 hroom body learning and memory center in the Drosophila brain protects against locomotion and short-t

52 ntify two neuronal types, P9 and BPN, in the Drosophila brain that, upon activation, initiate and mai

53 involved in long-term memory formation, from Drosophila brains, characterised their function, and det

54 st-scan cyclic voltammetry in isolated adult Drosophila brains.

55 binding protein that has a conserved role in Drosophila, but it also needs to evolve quickly to restr

56 g upon detection of the dsRNA-binding VSR of Drosophila C virus (DCV).

57 Model organisms, such as Drosophila, can help to identify and characterize these

58 s a regulator of autophagic flux in multiple Drosophila cell types.

59 CRISPR-Cas9 knockout of VINR in Drosophila cells enhances DCV replication independently

60 ong nano-COP reads reveal that, in human and Drosophila cells, splicing occurs after RNA polymerase I

61 ranslates to neuron morphology, we mapped 18 Drosophila central brain lineages.

62 Rcd4 is a poorly characterized Drosophila centriole component whose mammalian counterpa

63 iously reported that moesin, the only ERM in Drosophila, controls mitotic morphogenesis and epithelia

64 Previous work has characterized how walking Drosophila coordinate the movements of individual limbs

65 We isolated aggregated Drosophila CPEB, Orb2, from adult heads and determined i

66 Structure modeling of the Drosophila CTLH complex suggests that substrate recognit

67 We identified several drosophila CYPs (dCYPs) whose knockdown reduced PCB 28-d

68 During the first 2 hours of Drosophila development, precisely orchestrated nuclear c

69 Drosophila DIP and Dpr proteins mediate neuronal targeti

70 Different types of Drosophila dopaminergic neurons (DANs) reinforce memorie

71 Over the past decade, the spotted wing Drosophila, Drosophila suzukii, has invaded Europe and A

72 Spotted wing drosophila, Drosophila suzukii, is a serious invasive pe

73 f the cerebellum and Purkinje cell protein 4 Drosophila DTB-specific cis-regulatory elements correspo

74 (Zld) help initiate zygotic transcription in Drosophila early embryos, but whether other factors supp

75 gate mtDNA into individual organelles in the Drosophila early germarium.

76 e how the BMP gradient is interpreted in the Drosophila embryo by combining live imaging with computa

77 atterns the dorsal-ventral axis of the early Drosophila embryo, and we found that an empirical descri

78 l morphology regulation in cell formation in Drosophila embryogenesis.

79 Using stripe 2 of the even-skipped gene in Drosophila embryos as a case study, we dissect the regul

80 We find that elevating Dishevelled levels in Drosophila embryos has paradoxical effects, promoting th

81 maging, and time-resolved ChIP-seq assays in Drosophila embryos were used to dissect the ERK-dependen

82 re we show that R-loops form at many PREs in Drosophila embryos, and correlate with repressive states

83 pathway were enriched in nascent myotubes in Drosophila embryos.

84 genetic events that drive cellularization in Drosophila embryos.

85 Dorsal in dorsal-ventral axis patterning of Drosophila embryos.

86 of conformational changes in Zelda-depleted Drosophila embryos; (3) patient-specific aberrant chroma

87 Catalytic-inactivating mutations within the Drosophila enhancer H3K4 mono-methyltransferase Trr and

88 Database of Interacting Protein (DIP) Human, Drosophila, Escherichia coli (E. coli), and Caenorhabdit

89 Here we show that the Drosophila estrogen-related receptor (dERR) directs a tr

90 ther, this work demonstrates that individual Drosophila exhibit idiosyncratic olfactory preferences a

91 te a set of 103 proteins individually in the Drosophila eye and identify several new molecules that c

92 We found a new role of M1BP in regulating Drosophila eye development.

93 Here we report a perinuclear MTOC in Drosophila fat body cells that is anchored by the Nespri

94 We show that Drosophila female germline stem cells (GSCs) provide a p

95 signals that control the mating decisions of Drosophila females.

96 A previous study has reported that the Drosophila Fit1 protein (an ortholog of kindlin-2) preve

97 lg), and Lethal giant larvae (Lgl) using the Drosophila follicle epithelium.

98 We investigated how this is achieved for Drosophila Follicle Stem Cells (FSCs) by spatially-restr

99 Rover and sitter allelic variants of the Drosophila foraging (for) gene differ in parasitoid wasp

100 is required for development and viability in Drosophila, functions as a regulator of autophagic flux

101 how that Med19 physically interacts with the Drosophila GATA TFs, Pnr and Serpent (Srp), in vivo and

102 entify akt1 and a previously uncharacterized Drosophila gene CG8108, which is homologous to the human

103 Neoplastic transformation in a Drosophila genetic model of epidermal growth factor rece

104 ased GWAS screen (using 156 strains from the Drosophila Genetic Reference Panel) to search for natura

105 not require specific expertise beyond basic Drosophila genetics and husbandry, and confocal microsco

106 s and in human erythropoiesis in vitro Using Drosophila genetics, we show that PSEDN members function

107 Me31B is a protein component of Drosophila germ granules and plays an important role in

108 in cell shape and alignment over time in the Drosophila germband predict the onset of rapid cell rear

109 Accordingly, Drosophila H3K36A and H3K36R mutants show reduced levels

110 Developing germ cells in Drosophila have an additional specialized organelle conn

111 Our results confirm that the Drosophila HD network contains the core components of a

112 we demonstrate novel PSEDN roles in vivo in Drosophila hematopoiesis and in human erythropoiesis in

113 Using Drosophila hematopoietic organ: lymph gland, we demonstr

114 rate that muscle-derived Pvf1 signals to the Drosophila hepatocyte-like cells/oenocytes to suppress l

115 Using Sindbis virus (SINV) in Drosophila, here we show that viral infections affect TE

116 Here, we show that Drosophila HLBs form through phase separation.

117 a dorsalis, is distantly related to both the Drosophila hobo element and the Activator element from m

118 way (HBP) and O-GlcNAc transferase (OGT) for Drosophila homeodomain-interacting protein kinase (Hipk)

119 Finally, loss of the Drosophila homologue Lasp from a subset of commissural n

120 e tumor suppressor function of UBR5 (HYD) in Drosophila, HYD suppressed dMYC-dependent overgrowth of

121 Loss of ESCRT function in Drosophila imaginal discs is known to cause neoplastic o

122 Like tissues of many organisms, Drosophila imaginal discs lose the ability to regenerate

123 to modulate a large variety of behaviors in Drosophila including feeding initiation, locomotion, agg

124 te transporter, is the mammalian ortholog of Drosophila INDY.

125 s of adenomatous polyposis coli (APC) causes Drosophila intestinal stem cells to form adenomas [9].

126 In adult Drosophila intestine, a well-studied model of homeostati

127 for measuring endogenous dopamine release in Drosophila, introducing chemogenetic and optogenetic exp

128 In addition, Drosophila is an excellent model for studying how damage

129 Phototransduction in Drosophila is mediated by phospholipase C (PLC) and Ca(2

130 protein required for neuronal development in Drosophila; it can promote neural wiring through homophi

131 In contrast to the role of Drosophila L(2)gl, Llgl1 depletion in cultured rat cardi

132 We used cross-species functional analysis of Drosophila Labial and its mouse HOX1 orthologs (HOXA1, H

133 s display low (30%) sequence similarity with Drosophila Labial.

134 restore neuronal morphology and function in Drosophila lacking endogenous Tao.

135 factory sensory neuron (OSN) function in the Drosophila larva.

136 Under conditions in which Drosophila larvae are terminally arrested, we have chara

137 Here, we found that Drosophila larvae lacking either the mirtron miR-1010 or

138 rized in a decision-associated CNS region in Drosophila larvae, and then decoded by a group of peptid

139 nsory neurons respond to contractions in the Drosophila larval body wall during crawling.

140 Using the early Drosophila larval brain, we asked whether nutrient-depen

141 n is also evident in mutant ATXN3-expressing Drosophila larval brains and eyes.

142 ne degradation pathway significantly extends Drosophila lifespan, causes alterations of metabolites a

143 In Drosophila, light-dependent degradation of the clock pro

144 We created Drosophila lines that contained galbut virus as the only

145 lyBox, a simple tracking system for assaying Drosophila locomotor activity rhythms and thought that i

146 fr, on associative memory in male and female Drosophila Loss of PDF signaling significantly decreases

147 The Drosophila lymph gland, the larval hematopoietic organ c

148 ising new insights into the heterogeneity of Drosophila macrophages revealing many similarities to th

149 The Drosophila male germline stem cell (GSC) lineage provide

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

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

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

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

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

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

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

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

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

159 e tracking and microrheology measurements in Drosophila melanogaster embryos.

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

161 Drosophila melanogaster females undergo a variety of pos

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

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

164 Drosophila melanogaster has historically been a workhors

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

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

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

168 Drosophila melanogaster is a powerful system for charact

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

191 In Drosophila melanogaster, OSNs expressing specific recept

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

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

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

195 Here, we address these problems using Drosophila melanogaster.

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

197 the neuroprotective effects of PI3K in adult Drosophila melanogaster.

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

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

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

201 we conducted a genetic suppressor screen in Drosophila melanogaster.

202 Here, we use a fully developed tissue, Drosophila midgut, and describe the morphologically dist

203 Pavarotti, the Drosophila MKLP1 orthologue, is a kinesin-like protein t

204 rtant determinants of neurodegeneration in a Drosophila model of LRRK2 PD.

205 Insights from this whole-animal Drosophila model provide a powerful approach towards the

206 solation between species of Diptera, such as Drosophila, mosquitoes and sand flies.

207 Previously, using the Drosophila motor system as a model, we found the classic

208 ng as a metabolic regulator in healthy adult Drosophila muscle.

209 Here, we show that Drosophila mutants in the homolog of the human CYFIP1, a

210 findings suggest that the slit diaphragm of Drosophila nephrocytes requires balanced endocytosis and

211 n cultured cells, primary patient cells, and Drosophila nephrocytes.

212 The Drosophila nervous system is ensheathed by a layer of ou

213 l description of this major component of the Drosophila nervous system.

214 Using Drosophila neuroblasts and human cancer cells to study m

215 In asymmetrically dividing Drosophila neuroblasts, the aPKC PBM is required for cor

216 taking a comparative approach that exploits Drosophila neurogenetics, our results provide a causal,

217 Here, we examine how Drosophila neuromuscular synapses grow to match the size

218 lls with unique cytoarchitectures, including Drosophila neurons, mouse muscle cells, and rodent oligo

219 a role for the condensin I subunit Cap-G in Drosophila neurons.

220 appaB-mediated immune response by regulating Drosophila NF-kappaB factor Relish expression.

221 Accordingly, Drosophila NF-kappaB Relish expression was increased by

222 A new study in Drosophila now reveals that distinct classes of mechanos

223 atic changes in the transcription program in Drosophila occurs with the transition from proliferating

224 t induction of cytokine unpaired 3 (upd3) in Drosophila oenocytes (hepatocyte-like cells) is the prim

225 gh the frustrated (zigzag) spin chain is the Drosophila of frustrated magnetism, our understanding of

226 ebrafish and salamanders) and invertebrates (Drosophila) offer insights into brain repair and quiesce

227 AcTrace at three neuronal connections in the Drosophila olfactory system.

228 ynaptic to postsynaptic neurons in the adult Drosophila olfactory system.

229 ocal accumulation of oskar (osk) mRNA in the Drosophila oocyte determines the posterior pole of the f

230 proach to analyze the polarity of MTs in the Drosophila oocyte, a cell that displays distinct Kinesin

231 Here, we demonstrate that three Drosophila opsins, Rh1, Rh4, and Rh7, are needed in gust

232 ocess occurs along a continuous front in the Drosophila optic lobe neuroepithelium to produce neural

233 The recent structural elucidation of ex vivo Drosophila Orb2 fibrils revealed a novel amyloid formed

234 pplied to single cells, cell monolayers, and Drosophila ovarioles highlights the NMBS's ability to dy

235 e sole Na(V) channel in both male and female Drosophila, para Despite being the only Na(V) channel in

236 mically growing somatosensory neurons in the Drosophila peripheral nervous system exhibit organ spari

237 HP6, an ortholog of Drosophila Persephone, activates both proHP8 and proPAP1

238 microvilli-based photosensitive organelle of Drosophila photoreceptor cells.

239 We found that increased expression of the Drosophila PICALM orthologue lap could rescue Abeta42 to

240 Here, we show that GAGA factor (GAF), a Drosophila pioneer-like factor, functions with both SWI/

241 Genetic studies demonstrate that the Drosophila PLK Polo kinase (Polo) is inhibited by the fe

242 Exposing replicated Drosophila populations to a novel temperature regime, we

243 a non-monotonic effect on odor responses in Drosophila projection neurons (PNs), where low concentra

244 By examining how the Drosophila pupal dorsal thorax epithelium responds to mo

245 In many animals including Drosophila, repressor alleles are produced by transposit

246 st time that olfactory associative memory in Drosophila requires signaling by Pigment-dispersing fact

247 Grindelwald in pigmented glial cells of the Drosophila retina leads to age-related degeneration of b

248 is required for structural integrity of the Drosophila retinal floor.

249 Model organism studies in yeast and Drosophila reveal an intriguing link between mitochondri

250 We found that Drosophila Rh50A is expressed in larval muscles and enri

251 iously found that three maternally deposited Drosophila RNA-binding proteins (ME31B, Trailer Hitch [T

252 In Drosophila, RNAi mediated knockdown of Alk led to decrea

253 Analysis of Drosophila roX2 lncRNA using this approach revealed that

254 Pairing this behavior with the wealth of Drosophila's genetic tools offers the possibility to stu

255 Structure-guided functional assays in Drosophila S2 cells confirmed a principal role of the NT

256 stinct mode of interaction through which the Drosophila semaphorin Sema1b and mouse Sema6A mediate bi

257 hat a neuronal class specified by one of the Drosophila sex determining genes, fruitless (fru), belon

258 portant behavioral isolating barrier between Drosophila simulans and D. sechellia: male mate choice.

259 Spermathecal gene products are required for Drosophila sperm storage and sperm viability, and a sper

260 the cilia during cytoplasmic ciliogenesis in Drosophila sperm.

261 Thus, the Drosophila spermathecal lineage is an exciting model for

262 Studies in Drosophila suggest aversive olfactory LTM is optimal aft

263 Characterization in Drosophila suggests that TRAPPC9 and MEF2C contribute to

264 he past decade, the spotted wing Drosophila, Drosophila suzukii, has invaded Europe and America and h

265 Spotted wing drosophila, Drosophila suzukii, is a serious invasive pest impacting

266 elease and facilitation is not applicable at Drosophila synapses.

267 We identified Drosophila Tao kinase, the ortholog of the ASD risk gene

268 tor agonists, here we demonstrate the use of Drosophila taste neurons heterologously expressing rat P

269 omain factors Pou2f1/Pou2f2, the homologs of Drosophila temporal identity factors nub/pdm2, regulate

270 sing ex vivo and in vivo imaging, we show in Drosophila that astroglial Ca(2+) signaling increases wi

271 Here we investigate neural circuits in Drosophila that process proprioceptive information from

272 Here, we show that in Drosophila the small ubiquitin-like protein SUMO and the

273 Initially discovered in Drosophila, the Hippo pathway has been implicated as an

274 In Drosophila, the polarity protein Lethal (2) giant larvae

275 are selectively eliminated from the growing Drosophila tissue through cell competition, a tumor-supp

276 mmunofluorescence and electron microscopy of Drosophila tissues demonstrate an accumulation of lysoso

277 We found here that C-terminally truncated Drosophila TnT (TpnT-CD70) retains binding of tropomyosi

278 daptive circuit-based mechanism that enables Drosophila to form sleep-dependent and sleep-independent

279 ity to live image de novo ECM development in Drosophila to quantify production from initiation to hom

280 Loss of Drosophila TRIM32, encoded by thin (tn), shows reduced l

281 play an important role in the activation of Drosophila TRP channels.

282 Introduction of these residues into Drosophila TRPA1 confers anesthetic inhibition.

283 our study reveals that, similar to mammals, Drosophila uses iron limitation as an immune defense mec

284 atterns in distinct neural cell types of the Drosophila visual system using genetic lines to access i

285 n visual contrast is widespread in the early Drosophila visual system, improving velocity estimation

286 definitions, and spatial boundaries for the Drosophila VNC that are consistent with other insects.

287 ere, we report the identification of VINR, a Drosophila VSR-interacting long non-coding (lnc) RNA tha

288 Importantly, SCA3 phenotype in Drosophila was completely amenable to PNKP complementati

289 latform for efficient Cas12a gene editing in Drosophila We show that Cas12a from Lachnospiraceae bact

290 Using a whole-brain EM dataset of a female Drosophila, we comprehensively determine the wiring logi

291 ae Although Ir21a mediates heat avoidance in Drosophila, we find it drives heat seeking and heat-stim

292 In Drosophila, we found that decapentaplegic (dpp), the hom

293 eriod for long-term olfactory habituation in Drosophila, which closes early in adulthood can, like th

294 diates (AIs) of complex I (CI) biogenesis in Drosophila will enable the characterization of the preci

295 Here we investigated how epithelia of the Drosophila wing disc respond to loss of Short stop (Shot

296 mechanisms to dose-dependent Hh signaling in Drosophila wing imaginal discs.

297 Growth of the Drosophila wing-a classic paradigm-is governed by two mo

298 e imaging of the TSM1 axon of the developing Drosophila wing.

299 f Wnt ligands in the orientation of hairs of Drosophila wings, an established system for the study of

300 We demonstrate a TARE drive in Drosophila with 88-95% transmission by female heterozygo