ライフサイエンスコーパス: fruit fly

1 onal image datasets of model organisms (e.g. fruit fly).

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

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

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

5 manipulate and study neural circuits in the fruit fly.

6 potential biocontrol techniques against this fruit fly.

7 des for a deoxynucleotide transporter in the fruit fly.

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

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

10 l networks underlying the behavior of larval fruit flies.

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

12 is responsible for increasing sleep in young fruit flies.

13 eptors function as neurotrophin receptors in fruit flies.

14 al and left-right coordination for wild type fruit flies.

15 rane proteins mediating phototransduction in fruit flies.

16 fruit preference and parasitoid avoidance in fruit flies.

17 otion salience' reveals simple rules used by fruit flies.

18 organisms, including bacteria, nematodes and fruit flies.

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

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

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

22 ompeting XSEs and ASEs arose as a theory for fruit flies a century ago.

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

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

25 Fruit fly abdominal pigmentation may represent an optima

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

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

28 onitor the daily activity cycle of tephritid fruit flies Anastrepha ludens over their lifetime.

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

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

31 tiated nervous system, and recent studies in fruit flies and mice reveal novel insights into the neur

32 anding the basis of mating and aggression in fruit flies and mice.

33 Replication of viral RNA genomes in fruit flies and mosquitoes induces the production of vir

34 ral RNAi by the related Flock house virus in fruit flies and nematodes and reveal a mammalian antivir

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

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

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

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

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

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

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

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

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

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

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

46 ed behavior in animals, namely in Drosophila fruit flies, and some of these results are presented her

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

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

49 cally charged honeybees, green bottle flies, fruit flies, aphids, and also water drops falling near w

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

51 Invasive tephritid fruit flies are a great threat to agriculture worldwide

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

53 Fruit flies are regularly infected by parasitoid wasps i

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

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

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

57 n model systems such as mouse, zebrafish and fruit fly are combining conditional genetics and optogen

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

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

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

61 Using a 193-nm pulsed excimer laser and the fruit fly as a model, we created observation windows (12

62 Whether you use the fruit fly as an experimental system or want to apply Dro

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

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

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

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

67 present a method for tracking each leg of a fruit fly behaving spontaneously upon a trackball, in re

68 ly targeted neurons in the intact Drosophila fruit fly brain and reveals electrical signals in neurit

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

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

71 ing a map of stereotyped neurite tracts in a fruit fly brain.

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

73 e technologies have been applied, namely the fruit fly, C. elegans, zebrafish and mouse, remains rela

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

75 A recent study reports that fruit flies carrying histone H3 lysine 27 (H3K27) mutati

76 Human and fruit fly CBS contain heme; however, the role for heme i

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

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

79 Thus, in fruit flies, different classes of RNA polymerase III pro

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

81 10A ensures that germline stem cells in male fruit flies divide to produce two sibling cells that are

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

83 al characteristics similar to the eye of the fruit fly Drosophila and other arthropod species.

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

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

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

87 The fruit fly Drosophila is a classic model organism to stud

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

89 d spectroscopic characterization of CBS from fruit fly Drosophila melanogaster (DmCBS) and the CO/NO

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

91 l for genetic and genomic information on the fruit fly Drosophila melanogaster and related fly specie

92 Studies in invertebrates have focused on the fruit fly Drosophila melanogaster and the nematode Caeno

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

94 rganic foods, we used the well-characterized fruit fly Drosophila melanogaster as a model system.

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

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

97 The fruit fly Drosophila melanogaster encounters ethanol in

98 The fruit fly Drosophila melanogaster exhibits robust odor-g

99 As the fruit fly Drosophila melanogaster expresses Tau proteins

100 ce requirements of Frizzled receptors in the fruit fly Drosophila melanogaster for canonical and plan

101 The fruit fly Drosophila melanogaster has become a valuable

102 The fruit fly Drosophila melanogaster has been established a

103 Research in the fruit fly Drosophila melanogaster has led to insights in

104 The fruit fly Drosophila melanogaster has long been used as

105 The fruit fly Drosophila melanogaster has only one histone H

106 Historically neglected, the gut of the fruit fly Drosophila melanogaster has recently come to t

107 The fruit fly Drosophila melanogaster is a good model to unr

108 The fruit fly Drosophila melanogaster is a model system for

109 The fruit fly Drosophila melanogaster is a widely used model

110 The fruit fly Drosophila melanogaster is an excellent model

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

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

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

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

115 The visual system of the fruit fly Drosophila melanogaster shares marked similari

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

117 aling but safe additive, camphor, caused the fruit fly Drosophila melanogaster to decrease camphor re

118 ratory-adapted population of the promiscuous fruit fly Drosophila melanogaster to partition the varia

119 We used the fruit fly Drosophila melanogaster to show that chronic e

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

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

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

123 In the fruit fly Drosophila melanogaster, as in mammals, acute

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

125 In the fruit fly Drosophila melanogaster, interlocked negative

126 In the fruit fly Drosophila melanogaster, RNA polymerase III tr

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

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

135 archically to regulate dorsal closure in the fruit fly Drosophila melanogaster.

136 ysfunction is also a feature of aging in the fruit fly Drosophila melanogaster.

137 nce the first description of learning in the fruit fly Drosophila melanogaster.

138 for thousands of genes in the model organism fruit fly Drosophila melanogaster.

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

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

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

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

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

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

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

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

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

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

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

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

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

154 In contrast, the genome of the fruit fly (Drosophila melanogaster) has been successfull

155 The fruit fly (Drosophila melanogaster) is an extensively us

156 The fruit fly (Drosophila melanogaster) is frequently applie

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

158 We found that wild-type strains of fruit flies, Drosophila melanogaster, display morning (M

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

160 nidate, and a metabolite in the heads of the fruit fly, Drosophila melanogaster .

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

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

163 ne the modulation of feeding behavior in the fruit fly, Drosophila melanogaster, and identify a pair

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

165 f functional resolution is attainable in the fruit fly, Drosophila melanogaster, due to the armamenta

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

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

168 Male mate choice has been reported in the fruit fly, Drosophila melanogaster, even though males of

169 In the fruit fly, Drosophila melanogaster, genetic and anatomic

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

171 The fruit fly, Drosophila melanogaster, has been used for de

172 The fruit fly, Drosophila melanogaster, has been used to stu

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

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

175 Recent work in the fruit fly, Drosophila melanogaster, has identified Pumil

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

177 The fruit fly, Drosophila melanogaster, is an excellent orga

178 The fruit fly, Drosophila melanogaster, is generally diurnal

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

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

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

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

183 d arousal-testing paradigms to show that the fruit fly, Drosophila melanogaster, transitions between

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

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

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

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

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

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

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

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

192 Fruit fly embryogenesis is one of the best understood an

193 ene expression from Drosophila melanogaster (fruit fly) embryogenesis.

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

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

196 Fruit flies evolved in tropical regions under stable lig

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

198 iter hemolymph volumes from individual adult fruit-flies for chemical analysis.

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

200 key challenges in annotating and retrieving fruit fly gene expression pattern images.

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

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

203 c binding sites for these factors within the fruit fly genome.

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

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

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

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

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

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

210 Fruit fly heart tubes deficient of the Drosophila Mfn or

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

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

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

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

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

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

217 y sensitive wing expansion decision of adult fruit flies is coordinated by a single pair of neuromodu

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

219 hermore, if infected, ethanol consumption by fruit fly larvae causes increased death of wasp larvae g

220 Given that Drosophila melanogaster fruit fly larvae consume yeasts growing on rotting fruit

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 ure to ethanol reduces wasp oviposition into fruit fly larvae.

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

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

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

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

228 Fruit flies love foods containing yeast.

229 Fruit fly males exhibit an elaborate courtship display t

230 In fruit flies, males sing to court females.

231 t peach cultivars (cvs) to the Mediterranean fruit fly (medfly), Ceratitis capitata, and the volatile

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

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

234 Odorant receptors (ORs) from moths, fruit flies, mosquitoes, and the honey bees have been de

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 compensation in mammals, with comparisons to fruit flies, nematodes, and birds.

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

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

240 Larvae of Drosophila melanogaster, a fruit fly of tropical origin with a weak innate capacity

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

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

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

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

245 perature regulation of circadian activity in fruit flies or other animals are enigmatic.

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

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

248 cal to the retrogene movement in mammals and fruit flies out of the X chromosome evolving testis func

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

250 roductive sterility system for the tephritid fruit fly pest, Anastrepha suspensa, is presented, based

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

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

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

254 d2, the only Activin subfamily R-Smad in the fruit fly, produces overgrown wing discs that resemble g

255 The method developed for the fruit fly provides a new tool to evaluate the concentrat

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

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

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

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

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

261 Different species of fruit flies share habitats but are believed to mate with

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

263 Male fruit flies sing to females with quiet, close-range wing

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

265 In fruit flies, sleep can be conveniently estimated by meas

266 Fruit fly snRNPs also fail to bind Ketel; however, the i

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

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

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

270 Recent evidence from the fruit fly suggests that anatomically distinct dopaminerg

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

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

273 tic techniques to identify visual neurons in fruit flies that detect approaching objects, and whose a

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

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

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

277 ctivation no after-potential D protein) from fruit fly, the PDZ7 domain of GRIP1 (glutamate receptor

278 oteomes: human, mouse, rat, mouse-ear cress, fruit fly, the S. pombe yeast, the E. coli bacterium and

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

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

284 We conclude that in fruit flies, Tolls are not only involved in development

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

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

287 r EM neuroimages of two organisms (mouse and fruit fly) using different histological preparations and

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

289 Fruit flies were raised on a diets consisting of extract

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

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

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

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

294 In the fruit fly, with the powerful genetic tools available, sm

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

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

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

298 r targeted gene knockout in bacteria, yeast, fruit fly, zebrafish and human cells.

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

300 far including budding yeast, nematode worm, fruit fly, zebrafish, rat and mouse, the project has set