ライフサイエンスコーパス: fruit fly

1 DS for 4 species (human, mouse, nematode and fruit fly).

2 gh a case study of gradient formation in the fruit fly.

3 in mammals also affect cardiac ageing in the fruit fly.

4 ian and seasonal patterns of behavior in the fruit fly.

5 neurons in the ventral nervous system of the fruit fly.

6 manipulate and study neural circuits in the fruit fly.

7 potential biocontrol techniques against this fruit fly.

8 des for a deoxynucleotide transporter in the fruit fly.

9 fectively used to control this Mediterranean fruit fly.

10 e implemented in the olfactory system of the fruit fly.

11 n motifs appear to be conserved in mouse and fruit fly.

12 t player in a subset of clock neurons of the fruit fly.

13 organisms, including bacteria, nematodes and fruit flies.

14 nt because it is required for development in fruit flies.

15 wo alleles of a key detoxification enzyme in fruit flies.

16 s function in species ranging from humans to fruit flies.

17 l networks underlying the behavior of larval fruit flies.

18 particles (NAPs) from imidacloprid (IMI) on fruit flies.

19 is responsible for increasing sleep in young fruit flies.

20 mulate the olfactory system in Drosophila or fruit flies.

21 vivo voltage imaging in mice, zebrafish, and fruit flies.

22 onmental water samples and in the ovaries of fruit flies.

23 many animals, including mice, zebrafish and fruit flies.

24 ransduction process are, however, scarce for fruit flies.

25 boundaries from high resolution Hi-C data in fruit flies.

26 ids in the brain of Drosophila melanogaster (fruit fly), a major invertebrate model system in biologi

27 ervasive in these butterflies as compared to fruit flies, a fact that curiously results in very simil

28 ster and an array of viruses that infect the fruit fly acutely or persistently or are vertically tran

29 olutionary advantage of adaptively divergent fruit fly aggression phenotypes from different environme

30 s both enhance aggressive behaviour in olive fruit flies, allowing them to achieve higher fighting su

31 tor was also used to transform the Caribbean fruit fly, Anastrepha suspensa, indicating a wide range

32 af-32 that are enriched in TAD boundaries in fruit flies and also several unreported motifs.

33 acid), are detected by animals as diverse as fruit flies and humans, consistent with a near-universal

34 Long-lived dietary restricted fruit flies and insulin-like-peptide mutants exhibit sma

35 form II, which is much faster acting against fruit flies and mosquitoes.

36 During exposure to anoxic stress, fruit flies and other poikilotherms enter into a reversi

37 n Drosophila melanogaster S2 cells and adult fruit flies and results in increased SG formation.

38 ORC2) declines with age in the brain of both fruit flies and rodents and that the loss of mTORC2-medi

39 In this study, we analyze the locomotion of fruit flies and show that this non-stereotyped behavior

40 lidated LEAP using videos of freely behaving fruit flies and tracked 32 distinct points to describe t

41 x novel viruses in the viromes of laboratory fruit flies and wild populations of two insect vectors:

42 hat Met restriction extends lifespan in both fruit flies and yeast, and that this effect requires low

43 pective, we explore some of the strengths of fruit flies and zebrafish for addressing fundamental can

44 e been analyzed in detail, especially in the fruit fly and desert locust, understanding of the organi

45 R) motifs that interact with CAF1s in yeast, fruit fly and mammals.

46 dy shape, whereas published knockouts of the fruit fly and mouse orthologous genes resulted in lethal

47 repsiptera and has recently been recorded in fruit fly and spider lineages.

48 We demonstrated in cultured neurons and in fruit fly and zebrafish larvae how single cells could be

49 poral resolution in Drosophila melanogaster (fruit fly) and Danio rerio (zebrafish) to quantify signa

50 nown proteins was validated in invertebrate (fruit fly) and vertebrate (mouse) models.

51 H2S production was observed in yeast, worm, fruit fly, and rodent models of DR-mediated longevity.

52 of model systems, including yeast, nematode, fruit fly, and zebrafish, and discuss emerging methods f

53 the combinatorial odor code supplied by the fruit fly antenna is a very simple one in which nearly a

54 Although fruit flies are a common laboratory model organism of ch

55 Fruit flies are a far cry from the quaint genetic model

56 e behavior, but examples of such behavior in fruit flies are rare.

57 However, tephritid fruit flies are responsible for both direct and indirect

58 Experiments on fruit flies are shedding new light on the evolution and

59 Barnacles and fruit flies are two prominent model marine and terrestri

60 is is one of the most economically important fruit flies around the world.

61 Although we focus on fruit flies as a case study, the framework for our simul

62 del parasites and five species of Drosophila fruit flies as model hosts.

63 analyses of chemosensory genes in the citrus fruit fly B. minax provided new insights for preventive

64 The citrus fruit fly Bactrocera (Tetradacus) minax is a major and d

65 rly steps of spiroacetal biosynthesis in the fruit fly Bactrocera cacuminata (Solanum fly) have been

66 interactions of olive and the obligate olive fruit fly (Bactrocera oleae), and alter the economics of

67 nsposable element isolated from the Oriental fruit fly, Bactrocera dorsalis, is distantly related to

68 We tested the olive fruit fly, Bactrocera oleae (Diptera: Tephritidae), as a

69 Queensland fruit fly, Bactrocera tryoni (Froggatt), is the most sig

70 nd compare our results to two routinely used fruit fly balancer chromosomes.

71 he presence of female sex pheromone of olive fruit fly before the onset of pest infestation in an orc

72 sleep to a single pair of neurons within the fruit fly brain and provide a system for investigating t

73 We questioned whether activity in the fruit fly brain is different during such closed-loop beh

74 identified a single pair of neurons in the fruit fly brain that directly senses 'blood' glucose lev

75 ts have created the most detailed map of the fruit fly brain to date, identifying over 25,000 neurons

76 In the developing fruit fly brain, a protein called Trithorax increases th

77 timulate wake-promoting clock neurons in the fruit fly brain.

78 s have long been known to attract laboratory fruit flies, but small spots, presumably common in the w

79 We manipulated the antennal function of fruit flies by ablating their aristae, forcing them to r

80 ow gene determines sex-specific behaviors in fruit flies by acting in the brain.

81 hanism that causes the 'Minute' phenotype in fruit flies can explain how organisms are able to elimin

82 Studying the auditory system of the fruit fly can reveal how hearing works in mammals.

83 nvasion and ageing studies-the Mediterranean fruit fly (Ceratitis capitata)- we investigated how age,

84 The Mediterranean fruit fly, Ceratitis capitata Wiedemann, is a deleteriou

85 insect pest species, including Mediterranean fruit fly, Ceratitis capitata.

86 erences in the inhibition pattern enable the fruit fly circuit to respond faster to heading changes w

87 Here, in a case study involving the fruit fly clock, we demonstrate that VRC analysis provid

88 The skeletal muscle of fruit flies communicates with other organs to prevent th

89 diseases, but high-resolution structures of fruit fly contractile proteins have not been determined.

90 rated TE libraries: Drosophila melanogaster (fruit fly), Danio rerio (zebrafish), and Oryza sativa (r

91 ed hyperactivity in Drosophila melanogaster (fruit fly), demonstrating that PLD mediates behavioral r

92 Moreover, our real data analysis of fruit fly developmental time course RNA-Seq data demonst

93 raconidae), that attack Rhagoletis pomonella fruit flies (Diptera: Tephritidae).

94 10A ensures that germline stem cells in male fruit flies divide to produce two sibling cells that are

95 During olfactory learning in fruit flies, dopaminergic neurons assign value to odor r

96 gh recent reports have demonstrated that the fruit flies Drosophila melanogaster are capable of visua

97 roblem of motion estimation, focusing on the fruit fly Drosophila and the mouse retina.

98 Using the fruit fly Drosophila as an example, we discuss recent wo

99 y relating field abundance of the rainforest fruit fly Drosophila birchii to ecological change across

100 Two new studies in the fruit fly Drosophila demonstrate unexpected molecular, a

101 oup of local, inhibitory interneurons in the fruit fly Drosophila key for filtering these cues.

102 Paraquat is thus frequently used in the fruit fly Drosophila melanogaster and other animal model

103 ve demonstrated that molecular clocks in the fruit fly Drosophila melanogaster are regulated differen

104 Whether you are using the fruit fly Drosophila melanogaster as an experimental sys

105 nd required for mesoderm invagination in the fruit fly Drosophila melanogaster but do not appear duri

106 The fruit fly Drosophila melanogaster exhibits robust odor-g

107 As the fruit fly Drosophila melanogaster expresses Tau proteins

108 The fruit fly Drosophila melanogaster has become a valuable

109 The fruit fly Drosophila melanogaster has long been used as

110 The fruit fly Drosophila melanogaster has only one histone H

111 Schretter et al. (2018) demonstrated in the fruit fly Drosophila melanogaster how an enzyme from spe

112 The fruit fly Drosophila melanogaster is a widely used model

113 The fruit fly Drosophila melanogaster is an excellent model

114 on of the tsetse fly antenna and that of the fruit fly Drosophila melanogaster One morphological type

115 ronal substrates of reward perception in the fruit fly Drosophila melanogaster prompted us to develop

116 pid life cycle, and genetic amenability, the fruit fly Drosophila melanogaster provides an attractive

117 Myc-induced cell-autonomous apoptosis in the fruit fly Drosophila melanogaster relies on an intergeni

118 Here we demonstrate that mate choice in the fruit fly Drosophila melanogaster results in the linear

119 A study in the fruit fly Drosophila melanogaster shows that satellite D

120 lumnar (LC) neurons in the optic lobe of the fruit fly Drosophila melanogaster to characterize diverg

121 Here, we used adults of the fruit fly Drosophila melanogaster to investigate the met

122 In this study, we used the fruit fly Drosophila melanogaster to show that developme

123 Among these is the common fruit fly Drosophila melanogaster, a well-established mo

124 the powerful genetic tools available in the fruit fly Drosophila melanogaster, an outline of the neu

125 Notably, SKI-1/S1P of arthropods, like the fruit fly Drosophila melanogaster, contains a shorter pr

126 In the fruit fly Drosophila melanogaster, interlocked negative

127 Alternative models, including the fruit fly Drosophila melanogaster, show remarkable simil

128 the latest reference genome assembly of the fruit fly Drosophila melanogaster, was released by the B

129 Using the fruit fly Drosophila melanogaster, we identified neurons

130 This mechanism is found in the fruit fly Drosophila melanogaster, where polyploid ovari

131 In the fruit fly Drosophila melanogaster, which shows a robust

132 ial behaviour in many species, including the fruit fly Drosophila melanogaster.

133 genes that are modulated upon mating in the fruit fly Drosophila melanogaster.

134 rs that influence aggressive behavior of the fruit fly Drosophila melanogaster.

135 mulation of dead neurons in the brain of the fruit fly Drosophila melanogaster.

136 asts) to the published neuroblast map of the fruit fly Drosophila melanogaster.

137 s depicting embryonic gene expression in the fruit fly Drosophila melanogaster.

138 tasis and ageing in the antennal ears of the fruit fly Drosophila melanogaster.

139 find that Sir2 in the mushroom bodies of the fruit fly Drosophila promotes short-term ethanol-induced

140 he nematode worm Caenorhabditis elegans, the fruit fly Drosophila, and mice.

141 In the fruit fly Drosophila, head formation is driven by a sing

142 Here, we demonstrate that in the fruit fly Drosophila, the illusory motion percept is gen

143 our DNNto data from the early embryo of the fruit fly Drosophila, this system serves as a test bed f

144 ageing in laboratory animals, including the fruit fly Drosophila.

145 For example, fruit flies (Drosophila melanogaster) avoid an odor afte

146 contrast, Ae1a was lethal to closely related fruit flies (Drosophila melanogaster) but induced no adv

147 re and function of mitochondria in mouse and fruit flies (Drosophila melanogaster) by electron cryo-t

148 of the contact insecticidal activity toward fruit flies (Drosophila melanogaster) indicates that For

149 able system, we expressed the human DISC1 in fruit flies (Drosophila melanogaster).

150 d the antennal movement from tethered flying fruit flies (Drosophila melanogaster).

151 ystem (ALTOMS) for studying social memory in fruit flies (Drosophila melanogaster).

152 al motion and shape wing steering efforts in fruit flies (Drosophila).

153 asm, which contributes to embryo polarity in fruit flies (Drosophila).

154 d stability of bacterial colonization in the fruit fly (Drosophila melanogaster) gut.

155 o knock down gene expression in complex I in fruit fly (Drosophila melanogaster) neurons resulted in

156 ntegrin (the alphaPS3 integrin, scab) in the fruit fly (Drosophila melanogaster) suggests that gastru

157 In human (Homo sapiens), fruit fly (Drosophila melanogaster), and yeast (Saccharo

158 Fruit flies, Drosophila melanogaster, can perform this f

159 essed in a subset of foreleg neurons in male fruit flies, Drosophila melanogaster, rapidly and revers

160 chanism is highly reminiscent of that of the fruit fly, Drosophila melanogaster Altogether, our work

161 etary protein after modest starvation in the fruit fly, Drosophila melanogaster, and identified trypt

162 ts the community of researchers that use the fruit fly, Drosophila melanogaster, as a model organism.

163 In the fruit fly, Drosophila melanogaster, aversive olfactory l

164 nvestigate the temperature preference of the fruit fly, Drosophila melanogaster, during infection wit

165 We used replicated genetic lines in the fruit fly, Drosophila melanogaster, each characterized b

166 The fruit fly, Drosophila melanogaster, exhibits consolidate

167 The developing eye of the fruit fly, Drosophila melanogaster, has become a premier

168 The fruit fly, Drosophila melanogaster, has helped us to und

169 Research using the fruit fly, Drosophila melanogaster, has helped us unders

170 The fruit fly, Drosophila melanogaster, has proven to be a v

171 The fruit fly, Drosophila melanogaster, is well poised as a

172 In the fruit fly, Drosophila melanogaster, mating and the recei

173 In the fruit fly, Drosophila melanogaster, Pax6 also functions

174 In the fruit fly, Drosophila melanogaster, photoreceptors R7 an

175 Here, we show that akin to mammals, the fruit fly, Drosophila melanogaster, prefers food with a

176 In this study, we used the fruit fly, Drosophila melanogaster, to investigate how i

177 Using the fruit fly, Drosophila melanogaster, we found that sustai

178 rXs) Or10a, Or22a, and Or71a from the common fruit fly, Drosophila melanogaster, were recombinantly e

179 ageing have come from studying hearts of the fruit fly, Drosophila melanogaster.

180 (TpnC) genes that are expressed in the adult fruit fly, Drosophila melanogaster: TpnC4 is predominant

181 LDI-MS) is used to image brain lipids in the fruit fly, Drosophila, a common invertebrate model organ

182 highly conserved central brain region in the fruit fly, Drosophila, during flight.

183 we also pay particular attention to the tiny fruit fly, Drosophila, where new tools are creating new

184 Communication between male and female fruit flies during courtship is essential for successful

185 hat no viral-derived piRNAs were produced in fruit flies during different types of viral infection.

186 Spatial patterns in the early fruit fly embryo emerge from a network of interactions a

187 ia, whole-mount nematode larvae, whole-mount fruit fly embryos, whole-mount sea urchin embryos, whole

188 is required for the development of the adult fruit fly epidermis.

189 Fruit flies evolved in tropical regions under stable lig

190 en a choice among blue, green and dim light, fruit flies exhibit an unexpectedly complex pattern of c

191 ate hemizygosity of the X chromosome in male fruit flies, expression of X-linked genes increases twof

192 etermining the natural origin of Tephritidae fruit flies for which only the wing is suitable for anal

193 Before consenting to copulate, a female fruit fly gauges both her mating status and her suitor's

194 The Drosophila melanogaster (fruit fly) gene Diap1 encodes a protein referred to as D

195 Balancer chromosomes are tools used by fruit fly geneticists to prevent meiotic recombination.

196 roach that combines Drosophila melanogaster (fruit fly) genetics with transcriptome analyses it was f

197 Single-cell RNA sequencing in fruit flies gives an unprecedented picture of how new ge

198 rganizational principles governing how dirty fruit flies groom their bodies with sequential movements

199 ies constructed from the core members of the fruit fly gut microbiota.

200 ay from the mushroom bodies in the brains of fruit flies has improved our understanding of the ways i

201 However, the fruit fly has been exploited to recapitulate PD gene rel

202 osophila melanogaster, commonly known as the fruit fly, has been instrumental in genetics research an

203 To survive these environments, fruit flies have adapted mechanisms of tolerance that al

204 Genetic studies in fruit flies have implicated the chromatin remodeling com

205 s of the Central Complex in the brain of the fruit fly have identified neurons with activity that tra

206 errets, rabbits, pigs, sheep, zebrafish, and fruit flies, have all been used to model CF disease.

207 s virus replication in both female wasps and fruit fly hosts.

208 city in human cells and neurodegeneration in fruit flies, impairing eclosion and decreasing life span

209 To determine if fruit flies implement filtering driven by background opt

210 We probed the behavior of male and female fruit flies in a circular arena as individuals and withi

211 ependent phenotypes in both larvae and adult fruit flies, including locomotor activity, degeneration

212 porter-ameliorated HD-relevant phenotypes in fruit flies, including neurodegeneration and life expect

213 exists in the chordate amphioxus and in the fruit fly, indicating that a core MHC region predated th

214 systems, the long germband embryogenesis of fruit flies is an evolutionary derived state restricted

215 pase-9 in mammals or its ortholog, Dronc, in fruit flies, is facilitated by a multimeric adaptor comp

216 Drosophila melanogaster, a fruit fly, is an exquisite model organism to understand

217 In fruit flies, juvenile hormone (JH) induces intestinal st

218 tigate which of the only 10,000 neurons of a fruit fly larva can tip the balance in this trade-off, a

219 ges in most organisms is challenging; even a fruit fly larva has ~50,000 cells and a small mammal has

220 normal corrective response displayed by the fruit fly larva when turned upside down (self-righting).

221 modeling to study how the nervous system of fruit fly larvae processes sensory information to contro

222 controls the muscle contractions that allow fruit fly larvae to crawl.

223 irst time, accumulation of hydrazine in live fruit-fly larvae using epifluorescence microscopy.

224 The finding was made in Drosophila (fruit fly) larval motor neurons through a combined phara

225 udy of DNA protection in active chromatin of fruit fly, leading to a conclusion that the three PANS a

226 For a fruit fly, locating fermenting fruit where it can feed,

227 Fruit flies love foods containing yeast.

228 Fruit fly males exhibit an elaborate courtship display t

229 In fruit flies, males sing to court females.

230 The Mediterranean fruit fly (medfly), Ceratitis capitata, is a major destr

231 To analyze these data in the context of fruit fly metabolic networks, we developed Flyscape, an

232 protection conferred by TDO inhibition in a fruit fly model of Huntington's disease and that TRP tre

233 e used systematic behavioral measurements of fruit fly motion perception to show how flies combine lo

234 Finally, using fruit fly, mouse and macaque connectomes, we provide fur

235 ce of all stereotyped behaviors performed by fruit flies moving in a shallow arena.

236 dult muscle precursors (AMPs), the transient fruit fly muscle stem cells.

237 eukaryotic species-humans, mice, zebrafish, fruit flies, nematodes, and budding yeast.

238 Fruit fly neuroblasts can either self-renew, rest or tak

239 In the ventral nerve cord of fruit flies, neurons from the same hemilineage use the s

240 We discovered that the fruit fly olfactory circuit solves this problem with a v

241 e, we follow known circuit mechanisms in the fruit fly olfactory system to derive a simple algorithm

242 interneurons in the first brain relay of the fruit fly olfactory system.

243 In the fruit fly, one of the gluconeogenic genes, glucose-6-pho

244 We show that in male fruit flies, onset of the daytime siesta is delayed by a

245 In the fruit fly optic lobe, T4 and T5 cells represent the firs

246 earchers have documented the presence of the fruit fly or Drosophila melanogaster on alcohol-containi

247 tural pest Ceratitis capitata (Mediterranean fruit fly, or Medfly), we identified a Y-linked gene, Ma

248 iate in vitro with Hrp38/Hrb98DE/CG9983, the fruit fly ortholog of the human hnRNP A1/A2 factors.

249 ning monoubiquitin in vivo We found that the fruit fly orthologue of USP5 has catalytic preferences s

250 allenges we advance a comprehensive model of fruit fly OSNs as a cascade consisting of an odorant tra

251 ysis to quantify the probing behavior of the fruit-fly parasitoid Diachasmimorpha longicaudata (Braco

252 any metazoan species including human, mouse, fruit fly, planaria and flowering plants.

253 Thus, the nonluminescent fruit fly possesses an inherent capacity for bioluminesc

254 The larvae of fruit flies produce pheromones to control whether they a

255 ndings together with experimental results on fruit flies' reaction time and sensory motor reflexes, w

256 tiation promoters are pervasive in human and fruit fly, reflecting evolutionary conservation.

257 clin B3 homologues from frog, zebrafish, and fruit fly rescue meiotic progression in cyclin B3-defici

258 roups of insects-crickets, grasshoppers, and fruit flies-reveals common strategies for extracting eth

259 Understanding the logic behind how a fruit fly's brain tells it to groom its body parts in a

260 We found that fungus-infected fruit flies seek out cooler temperatures, which facilita

261 Learning based on what a fruit fly sees or what it smells might not involve disti

262 d sensory motor reflexes, we conjecture that fruit flies sense their kinematic states every wing beat

263 hey are also involved in taste perception in fruit flies, significantly expanding their scope of acti

264 ver chasms larger than step size is vital to fruit flies, since foraging and mating are achieved whil

265 A newly-identified fruit fly sleep-regulator is also an AMP.

266 new study by Berry et al. indicates that, in fruit flies, sleep accomplishes this in part by preventi

267 2 Zeugodacus cucurbitae; three invasive pest fruit fly species with overlapping hostplants.

268 ed several billion small RNA reads across 12 fruit fly species.

269 Here we show that Drosophila melanogaster (fruit fly) subject to obesogenic challenges exhibits met

270 ficities function in cell types not found in fruit flies, suggesting that evolution of TF specificiti

271 A new study in fruit flies suggests modulation of neural activity links

272 the eye and its target neuropils in fish and fruit flies supports a homology between some core elemen

273 Inhibition of Nuak1 in fruit flies suppressed neurodegeneration in tau-expressi

274 During pathogen infection, fruit fly survival varies directly with sleep.

275 hange in the temperature preference of adult fruit flies that results from a shift in the relative co

276 f Wolbachia wMelPop (a bacterial symbiont of fruit flies) that differed in copy number of a region of

277 In the fruit fly, the large lateral ventral neurons (lLNvs) are

278 ntified motor neurons control flexion of the fruit fly tibia.

279 kappaB plays a central role in immunity from fruit flies to humans, and NF-kappaB activity is altered

280 tate motion by a wide range of animals, from fruit flies to humpback whales, operating in either air

281 We find a conserved role, from fruit flies to mammals, for L-type calcium channels in a

282 inds that viewing small spots causes walking fruit flies to stop in their tracks, and identifies the

283 ge tracing and genetic analysis in the adult fruit fly to gain new insight into the cellular and mole

284 that are conserved in orthologs ranging from fruit fly to human.

285 cts that replace native introns of human and fruit fly tRNA genes with the Broccoli fluorescent RNA a

286 a novel stimulus that initially interests a fruit fly turns into a familiar one.

287 have measured the temperature preference of fruit flies under different pathogen conditions.

288 e apply CNEr to two novel genome comparisons-fruit fly vs tsetse fly, and two sea urchin genomes-and

289 From studies beginning in fruit flies, we now know that circadian regulation perva

290 ned families of the Ig superfamily (IgSF) in fruit flies were discovered to label different subsets o

291 Dissected wings from Drosophila melanogaster fruit flies were used as the hydrophobic, laser energy s

292 ntegration required for odor localization in fruit flies, which may be representative of adaptive mul

293 leep-dependent slow wave oscillations in the fruit fly, which act to inhibit sensory input during sle

294 undly suppresses aggressive behaviors in the fruit fly, while other social behaviors are unaffected.

295 A mature virgin female fruit fly will initially resist copulation, while she as

296 n aerodynamic forces, and furthermore that a fruit fly, with nearly massless wings, would not exhibit

297 ed our motif database for human, mouse, rat, fruit fly, worm, yeast and Arabidopsis, and curated larg

298 Pch2 homologs are present in fruit flies, worms, and mammals, however the molecular m

299 namics of volumes of neurons and synapses in fruit flies, zebrafish larvae, mice and ferrets in vivo.

300 mensional, terabyte-sized image data sets of fruit fly, zebrafish and mouse embryos acquired with thr