ライフサイエンスコーパス: cricket

1 of hand injury prevention strategies within cricket.

2 produces neurons throughout the life of the cricket.

3 generated sound in a sonorously stridulating cricket.

4 d a lipid content 1.5 fold higher than house cricket.

5 r of a phylogenetically basal insect, a tree cricket.

6 rrespond to regional grouping of conspecific crickets.

7 related within eastern North American field crickets.

8 ts and in noctuid moths, but it differs from crickets.

9 estrained reach-to-grasp task involving live crickets.

10 insect species and tebuconazole residues in crickets.

11 Here, we ask why baffling is uncommon among crickets.

12 urring may allow private communication among crickets.

13 (ICP-MS) and compared with that of beef and crickets.

14 conversion ratio and weight of the harvested crickets.

15 ing from sexual trait reversal in wild field crickets.

16 milar to those produced by female lebinthine crickets.

17 ed between, species to explore speciation in crickets.

18 .08 ug/100 g for mealworm, 2.88 ug/100 g for cricket, 0.84 ug/100 g for grasshopper, and 13.2 ug/100

19 zed the DNA sequence of the Pgi gene from 29 crickets (15 G. veletis and 14 G. pennsylvanicus).

20 ched with intrinsically (67)Zn-labeled house crickets (2.61 mg Zn, n = 28) in comparison with meals e

21 d from refined maize porridge with unlabeled crickets (4.92%) was lower than from the reference meal

22 Exceptions include bird-,(3)(,)(4) cricket-,(5)(,)(6) and mammal-dispersed(7) species, feat

23 ze flour porridge with either [57Fe]-labeled crickets, [58Fe]SO4 (reference meal), or unlabeled crick

24 In cricket, a batsman watches a fast bowler's ball come tow

25 In Hawaiian populations of the Pacific field cricket, a new morph producing a novel and incredibly va

26 In this study, insect proteins of cricket Acheta domesticus and mealworm Tenebrio molitor

27 Each cercus in the common house cricket Acheta domesticus is covered with between 500 to

28 The allergenic potency of the cricket Acheta domesticus, a promising edible insect, ha

29 value and chemical composition of the house cricket (Acheta domestica L.).

30 ellow mealworm (Tenebrio molitor), the house cricket (Acheta domesticus) and the migratory locust (Lo

31 In common house crickets (Acheta domestica) the hairs cover two antenna-

32 activity against flies (Musca domestica) and crickets (Acheta domestica).

33 sessed fractional iron absorption from house crickets (Acheta domesticus) consumed with refined (low-

34 As mealworms (Tenebrio molitor) and crickets (Acheta domesticus) have recently become commer

35 aimed at improving the knowledge on powdered crickets (Acheta domesticus).

36 tissue from each treatment was used to feed crickets (Acheta domesticus).

37 content in mealworms (Tenebrio molitor) and crickets (Acheta domesticus).

38 ges, and male and female adults of the house cricket, Acheta domesticus.

39 gnal, was first inspired by the evolution of cricket acoustic communication nearly 50 years ago.

40 of the members of a wild population of field crickets across two generations to capture the factors p

41 We used the crickets Allonemobius fasciatus and A. socius to investi

42 In the striped ground cricket, Allonemobius socius, females are the larger sex

43 e show that a father's mating success in the cricket, Allonemobius socius, is positively genetically

44 vory-like taste profiles (27 descriptors for cricket and 39 descriptors for mealworm protein).

45 insect species (mealworm, grasshopper, house cricket and black soldier fly) analyzing a large spectru

46 For both the mealworm, grasshopper, house cricket and black soldier fly, 64, 61, 59 and 62 compoun

47 alify them as descending giant fibers in the cricket and suggest an involvement in evoking fast locom

48 ouse cricket, banded cricket, Jamaican field cricket and two-spotted cricket was studied using high-t

49 arget species: two bands (40 and 14 kDa) for crickets and a pattern including light responses at 17,

50 ysiological systems such as the receptors in crickets and crayfish.

51 otypes for pulse duration and pause known in crickets and even other insects.

52 Iron absorption from house crickets and fortified maize porridge with crickets is l

53 pecies with greatly enlarged T3 leg, such as crickets and grasshoppers, and species that exhibit more

54 nile hormone biosynthesis in cockroaches and crickets and inhibition of contraction of certain insect

55 Mormon crickets and juvenile locusts form huge migratory bands-

56 is consistent with known preference types in crickets and other insects, and arises from computations

57 Crickets and other orthopteran insects sense air current

58 Studies on aphids, crickets and planthoppers have revealed that alternative

59 Several new studies on crickets and social bees have now shown how insects can

60 metabolous species, Acheta domesticus (house cricket) and Periplaneta americana (cockroach), and re-e

61 RC enrolled in 4 Italian trials (CAVE, VELO, CRICKET, and CHRONOS) and treated with anti-EGFR rechall

62 Beetles, crickets, and ants exhibited rapid cycles of tracheal co

63 he CC led to malformed chirping movements by crickets, and pharmacological stimulation evoked stridul

64 have been performed in locusts, cockroaches, crickets, and stick insects, the examples we cite here a

65 Female crickets appear to have evolved a simple but effective s

66 Mormon crickets appear to occur in two phases that differ in mo

67 Female field crickets approach the low-frequency calling song of male

68 House crickets are expected to play a significant role in the

69 However, crickets are much smaller than the wavelength of their c

70 We have examined how the crickets' ascending auditory pathway copes with self-gen

71 Male crickets attract females by producing calls with their f

72 Axonal terminals of bush-cricket auditory afferents received 2-5 mV graded depola

73 The cricket auditory system has to deal with highly stereoty

74 uitoes afford highly sensitive ears, and how crickets avoid deafening themselves with their songs.

75 le from materials such as a tennis ball, red cricket ball and cricket glove.

76 The variation in lipidome of house cricket, banded cricket, Jamaican field cricket and two-

77 erties, could be used for the development of cricket-based protein ingredients for food formulations.

78 te the effects of mating on female decorated cricket baseline immunity and the potential for a male-g

79 esence of chitin and other inhibitors in the cricket biomass.This trial was registered at as NL6821.

80 Temporal pattern recognition in the cricket brain occurs within the anterior protocerebrum a

81 An examination of both developing and adult cricket brains showed that sema2a mRNA and protein were

82 nt activities were significantly enhanced in cricket breads, indicating that cricket powder provides

83 ng structural resonance for sound radiation, crickets broadcast species-specific songs at a sharply t

84 ease in efficiency is accessible not just to crickets but to all acoustically communicating animals w

85 ce in male and female Gryllus texensis field crickets by manipulating diet quality via nutrient conte

86 Categorical perception was tested in crickets by using two paradigms of human psychophysics,

87 use a resonant system to produce sound, tree crickets can produce high amplitude songs at different f

88 pite their small size, some insects, such as crickets, can produce high amplitude mating songs by rub

89 to Gregarina niphandrodes suggest that these crickets carry the parasite.

90 ion persist in a fictively singing, isolated cricket central nervous system and are therefore the res

91 anosensory receptors and interneurons in the cricket cercal sensory system are sensitive to the direc

92 ly selective mechanosensory afferents in the cricket cercal sensory system form a map of air current

93 ameters by sensory interneurons (INs) in the cricket cercal sensory system.

94 in two types of sensory interneurons in the cricket cercal system.

95 From simple cricket chirps to more elaborate bird songs, animals go

96 3%), and did not differ for the 2 meals with crickets compared with the reference meal.

97 Feces from control, bulk, and NP-exposed crickets contained Ce at 248, 393, and 1010 ng/g, respec

98 ional geometries of the tracheae of the bush cricket Copiphora gorgonensis.

99 worm (MWP), migratory locust (LP), and house cricket (CP) are novel foods recently authorized by the

100 at were important to biological processes in cricket development.

101 Tree crickets differ sharply from this scheme.

102 The results show that crickets divide sound frequency categorically between at

103 us viridescens), in schistosomes and in cave crickets (Dolichopoda species).

104 In one group of crickets (Eneopterinae: Lebinthini), however, males prod

105 The results showed that cricket-enriched doughs and the standard had similar fer

106 Cricket enrichment conferred to the breads a typical fla

107 e diversity of acoustic signaling systems in crickets exemplifies the evolution of elaborate male dis

108 We also show that the tree cricket exploits critical oscillator-like mechanics, ena

109 Crickets fed NP CeO2-exposed zucchini leaves contained s

110 recognition in crickets shows that decorated cricket females use self-referenced recognition informat

111 with intrinsically (67)Zn-labeled low-chitin cricket flour (2.51 mg Zn, n = 25), whereas the secondar

112 imed to evaluate different pre-treatments on cricket flour (CF), solvent-defatting (CFH), and supercr

113 In this work, cricket flour was used to produce gluten-free sourdough

114 our efforts to provide genetically improved crickets for human consumption and livestock feed.

115 nt in future studies of genetically modified crickets for improved food production, including those i

116 w that it is the distinctive geometry of the crickets' forewings (the resonant system) that is respon

117 Spiders that consumed crickets from control or bulk treatments contained nonqu

118 (PO) activity, and encapsulation ability of crickets from eight inbred lines with that of crickets f

119 genes, COII and COIII, in samples of Mormon crickets from gregarious populations west of the contine

120 Surprisingly, crickets from inbred lines had a greater encapsulation a

121 rickets from eight inbred lines with that of crickets from the outbred founder population.

122 greater encapsulation ability compared with crickets from the outbred population.

123 genomics and a high-quality chromosome-level cricket genome.

124 tive incompatibility exist among taxa of the cricket genus Gryllus.

125 ggested that diversification of the Hawaiian cricket genus Laupala was initiated by single invasions

126 coustic preference variation in the Hawaiian cricket genus Laupala.

127 he commonality of BMP signaling in mouse and cricket germ cell induction, we suggest that BMP-based g

128 such as a tennis ball, red cricket ball and cricket glove.

129 neural recordings in three groups of insects-crickets, grasshoppers, and fruit flies-reveals common s

130 In this study, whole crickets (Gryllodes sigillatus) were hydrolyzed with alc

131 ical consequences of inbreeding in decorated crickets, Gryllodes sigillatus, by comparing lytic activ

132 Here, we show that the cricket Gryllus bimaculatus has a different solution to

133 We show that primordial germ cells of the cricket Gryllus bimaculatus transduce BMP signals and re

134 In the cricket Gryllus bimaculatus, a member of the hemimetabol

135 Here, we show that in the cricket Gryllus bimaculatus, an evolutionarily distant o

136 show that in a basally branching insect, the cricket Gryllus bimaculatus, conserved germ plasm molecu

137 erved in both the mouse Mus musculus and the cricket Gryllus bimaculatus, which is an emerging model

138 is not required for segment formation in the cricket Gryllus bimaculatus, which retains ancestral cha

139 ere, we characterize sema1a and plexA in the cricket Gryllus bimaculatus.

140 formation from the head to the thorax in the cricket Gryllus bimaculatus.

141 iance in sperm size and number traits in the cricket Gryllus bimaculatus.

142 artificial selection of sperm length in the cricket Gryllus bimaculatus.

143 needle-shaped nucleus of the emerging model cricket Gryllus bimaculatus.

144 entally induced seasonal environments in the cricket Gryllus bimaculatus.

145 ortholog in a basally branching insect, the cricket Gryllus bimaculatus.

146 The field crickets Gryllus firmus and G. pennsylvanicus exhibit a

147 B(12) in mealworm (Tenebrio molitor larvae), cricket (Gryllus assimilis), grasshopper (Locusta migrat

148 ity between Macrobrachium spp. and the field cricket (Gryllus bimaculatus) is necessary for food safe

149 The onset of chill-coma in the fall field cricket (Gryllus pennsylvanicus, Orthoptera: Gryllidae)

150 from contaminated carrots by Jamaican field crickets (Gryllus assimilis) and yellow mealworms (Teneb

151 locusts (Locusta migratoria) and two-spotted crickets (Gryllus bimaculatus) as well as to subsequentl

152 laboratory population of Mediterranean field crickets (Gryllus bimaculatus), in which both explorator

153 n of individually marked and genotyped field crickets (Gryllus campestris).

154 et of the corresponding abdominal neurons in crickets (Gryllus, Orthoptera), the ecdysial cGMP respon

155 on and plasticity in the life history of the cricket, Gryllus firmus.

156 closely related eastern North American field crickets, Gryllus firmus and G. pennsylvanicus, hybridiz

157 Two species of crickets, Gryllus veletis and G. pennsylvanicus, share s

158 n identical conditions, two-spotted & banded crickets had a lipid content 1.5 fold higher than house

159 A new study of crickets has found that females mark their mates to avoi

160 We suggest that because inbred crickets have reduced reproductive effort, they may, the

161 Bush crickets have tympanal ears located in the forelegs.

162 rdings of extrinsic neurons in the brains of crickets, honey bees, and cockroaches.

163 nge of sensitivities to the frequency of the cricket host's calling song frequency.

164 520 mum, to pinpoint the 5 kHz chirp of its cricket host.

165 In lebinthine crickets, however, we found that auditory ascending neur

166 seen when females were allowed to consume a cricket in lieu of a male, suggesting that it is the con

167 ion, football in the English Premier League, cricket in the Indian Premier League and baseball in Maj

168 e tested the baffle-making behaviour of tree crickets in a series of experimental contexts.

169 Thus, Cricket is a game of skill for individuals and a game of

170 e crickets and fortified maize porridge with crickets is low, which may be explained by the presence

171 Phonotactic orientation of female crickets is tuned to the temporal pattern of the male ca

172 riation in lipidome of house cricket, banded cricket, Jamaican field cricket and two-spotted cricket

173 ludes many familiar singing insects, such as crickets, katydids, and grasshoppers.

174 Beetles, mantids, true crickets, mole crickets, katydids, green lacewings, and locusts have an

175 nisms of evolutionary interest, the Hawaiian cricket Laupala genome is not well characterized genetic

176 t of biologically inspired robots performing cricket-like auditory orientation.

177 A small group called tree crickets make acoustic tools called baffles which reduce

178 Even though the recovery of GlcN from spiked cricket material was slightly lower compared to that usi

179 This study evaluated the effect of cricket meal (CM) incorporation on the physicochemical,

180 Absorbed zinc from both cricket meals was higher than that from high-enriched me

181 The auditory neuropil of the bush-cricket Mecopoda elongata is tonotopically organized, wi

182 Beetles, mantids, true crickets, mole crickets, katydids, green lacewings, and

183 nvertebrates, including shrimp, cockroaches, crickets, moths, crayfish, and sea stars.

184 their gross morphology is similar to that of cricket omega cells.

185 As predicted, crickets on a high-quality diet eclosed more quickly, an

186 Crickets on a high-quality diet were not in better condi

187 We found that given the opportunity, tree crickets optimised baffle acoustics; they selected the b

188 Here, we show that tree-crickets optimize acoustic baffles, objects that are use

189 rothoracic limb in two other winged insects, crickets (Orthoptera) and milkweed bugs (Hemiptera), is

190 survival after DCV infection, but also after cricket paralysis virus (CrPV) and flock house virus (FH

191 An IRES element in cricket paralysis virus (CrPV) can directly assemble 80S

192 The cricket paralysis virus (CrPV) intergenic region interna

193 The cricket paralysis virus (CrPV) intergenic region IRES (I

194 onavirus mRNAs, hepatitis C virus (HCV), and cricket paralysis virus (CrPV) IRES-driven mRNAs that ar

195 The cricket paralysis virus (CrPV) uses an internal ribosoma

196 The cricket paralysis virus (CrPV), a member of the CrPV-lik

197 Like the IRES in cricket paralysis virus (CrPV), the TSV IRES can assembl

198 pathogen, Drosophila C virus (DCV), and with Cricket Paralysis virus (CrPV).

199 The intergenic IRES of Cricket Paralysis Virus (CrPV-IRES) forms a tight comple

200 In this study, we identify the dicistrovirus cricket paralysis virus 1A (CrPV-1A) protein that functi

201 tly discovered IRES located in the genome of cricket paralysis virus can direct the efficient transla

202 ribosome entry site located in the genome of cricket paralysis virus can form 80S ribosomes without i

203 The dicistrovirus Cricket Paralysis virus contains a unique dicistronic RN

204 Thus, the cricket paralysis virus genome is an example of a natura

205 nfirmed that ribosomes that assembled on the Cricket paralysis virus intercistronic internal ribosoma

206 In this report, we show that the cricket paralysis virus intergenic internal ribosome ent

207 gated how a 40S subunit was recruited by the cricket paralysis virus intergenic region (CrPV IGR) IRE

208 ic amino acid transporter, cat-1, and of the cricket paralysis virus intergenic region, were stimulat

209 lly characterized at high resolution how the Cricket Paralysis Virus Internal Ribosomal Entry Site (C

210 The cricket paralysis virus internal ribosome entry site (Cr

211 binding to the A and P sites as well as the cricket paralysis virus internal ribosome entry site (IR

212 tiation complex formed by Nsp1, 40S, and the cricket paralysis virus internal ribosome entry site (IR

213 The cricket paralysis virus internal ribosome entry site (IR

214 Using the cricket paralysis virus internal ribosome entry site ele

215 driven by the classical swine fever virus or cricket paralysis virus internal ribosome entry sites (I

216 Therefore, the cricket paralysis virus IRES is likely to recruit riboso

217 ribosomal entry site (IRES) or an RNA with a cricket paralysis virus IRES.

218 Cricket paralysis virus is a member of a group of insect

219 in, called CrPV-1A, within the dicistrovirus cricket paralysis virus that can inhibit host transcript

220 ned the role of temperature on the growth of cricket paralysis virus, a member of the family Dicistro

221 flies to infection by Drosophila C virus and cricket paralysis virus, two members of the Dicistroviri

222 ibit the translation of a putative IRES from cricket paralysis virus.

223 ated viruses, encephalomyocarditis virus and cricket paralysis virus.

224 IRES from the intergenic region (IGR) of the Cricket Paralysis Virus.

225 ope, and the internal ribosome entry site of cricket paralysis virus.

226 resolution X-ray crystal structure of mature cricket parvovirus (Acheta domesticus densovirus [AdDNV]

227 inguished good from poor batsmen, and that a cricket player's eye movement strategy contributes to hi

228 ts, [58Fe]SO4 (reference meal), or unlabeled crickets plus [54Fe]SO4.

229 enhanced in cricket breads, indicating that cricket powder provides to bakery gluten-free goods high

230 basic nutritional composition revealed that cricket powders were rich in protein (42.0-45.8% of dry

231 nalyses into the proteins indicated that the cricket powders were treated with high temperatures and

232 lving rapid alteration of both the songs the crickets produce and the ability of eavesdropping flies

233 of whole, roasted whole and roasted powdered cricket products.

234 ies and antioxidant activities of conjugated cricket protein (CCPs) by wet heating Maillard reaction

235 The cricket protein (CP) samples pre-processed with microwav

236 and supercritical-defatting (CFS) to obtain cricket protein concentrate (CPC) by ultrafiltration (UF

237 ration processes were suitable for obtaining cricket protein concentrates.

238 e profile, structure and solubility of house cricket protein extracts.

239 perties demonstrate the potential to develop cricket protein hydrolysates as a source of functional a

240 The study was carried out to investigate cricket protein hydrolysates' (CPH) potential to enhance

241 he results suggested that the conjugation of cricket protein isolate (CPI) with MR is the most promis

242 with MR is the most promising way to improve cricket protein properties for food industry application

243 Different cricket proteins were detected by immunoblotting with sh

244 ethanol induced aggregation of non-blanched cricket proteins, with a 13-72% reduction in protein rec

245 Cricket-related hand injury was related to an increased

246 Data included history of cricket-related hand/finger injury leading to > 4 weeks

247 In field studies, female crickets respond positively to purrs, but eavesdropping

248 singing behavior of the Island's only field cricket, resulting in a coevolutionary arms race involvi

249 nse to self-generated sound and protects the cricket's auditory pathway from self-induced desensitiza

250 A recent study of social recognition in crickets shows that decorated cricket females use self-r

251 Haldane's rule for female sterility in field cricket sister species (Teleogryllus oceanicus and T. co

252 We recorded phonotaxis to a cricket song masked by band-limited noise.

253 wing mutation, flatwing, that eliminates the crickets' song, an important sexual signal, but protects

254 nd rapid diversification of their local host crickets' song.

255 We also demonstrate that field cricket species closely related to the Lebinthini show a

256 es that they can colonize, and that two bush cricket species show increased fractions of longer-winge

257 Although the four cricket species were reared in identical conditions, two

258 a clear north-south split within each of the cricket species, a pattern not seen for morphological or

259 In five cricket species, we analyzed the structure and activity

260 ation phylogeny for this pair of hybridizing cricket species.

261 e identified with no major differences among cricket species.

262 he singing central pattern generator in five cricket species.

263 atures and allowed the determination of four cricket-specific peptides that showed sufficient thermos

264 er-order genome organization in ultracompact cricket sperm, and establishes a multidisciplinary metho

265 New observations of wild field crickets suggest instead that guarding males provide pro

266 A study of tropical crickets suggests that a twitchy response to ultrasonic

267 ve germ cell specification between mouse and cricket supports the hypothesis that this molecular mech

268 hat for a set of male call properties in the cricket Teleogryllus commodus, the pattern of multivaria

269 signal in Hawaiian populations of the field cricket Teleogryllus oceanicus, which was brought about

270 lt traits in the continuously breeding field cricket Teleogryllus oceanicus: male mating tactics, rep

271 a labeled bursicon-containing neurons in the crickets Teleogryllus commodus and Gryllus bimaculatus,

272 of the 21st century in a population of field crickets (Teleogryllus oceanicus) on the Hawaiian island

273 nge in the sexual signal of Polynesian field crickets, Teleogryllus oceanicus, that recently colonize

274 -soluble protein from the integument of bush-cricket Tettigonia cantans.

275 her orthopteroid taxa (cockroaches, locusts, crickets, tettigoniids).

276 Laupala, a group of forest-dwelling Hawaiian crickets that is characterized primarily through differe

277 ecordings of auditory neurons in the singing cricket, that presynaptic inhibition of auditory afferen

278 method for measuring the movements of female crickets, that when walking and flying each sound pulse

279 In field crickets, the brain receives activity from two auditory

280 We show that in crickets, the eggs of females that mate only with siblin

281 include the allatostatins of cockroaches and crickets, the schistostatins of locusts, and the callato

282 ently assembled and annotated genome of this cricket, this knock-in/knockout method increases the via

283 alyzed the phonotactic selectivity of female crickets to varying temporal features of calling song pa

284 s preferentially sniffed model prey fish and crickets underwater by exhaling and reinhaling air throu

285 Crickets use their long antennae as tactile sensors.

286 e test this in a wild population of Hawaiian crickets using temporal genomics and a high-quality chro

287 kinematic relationships between the hand and cricket velocity revealed that predictions of the expect

288 cket, Jamaican field cricket and two-spotted cricket was studied using high-throughput screening tech

289 lso showed that tibial neuron development in crickets was comparable to that described in grasshopper

290 protein expression patterns in the embryonic cricket were similar to that seen in the grasshopper.

291 After 14 d, crickets were analyzed for Ce content or were fed to wol

292 Intrinsically [57Fe]-labeled and control crickets were reared.

293 study examines the indel spectrum in Laupala crickets, which have a genome size 11 times larger than

294 rat (Thysanura) and the leg patch is seen in crickets, which have no comb.

295 In female crickets, which orient towards the male's calling song,

296 EHD was applied to house crickets with and without PEF pretreatment, and the effe

297 Information on the lipidome of these crickets with high commercial value is important to esti

298 onal iron absorption from 57Fe-labeled house crickets with refined maize porridge (3.06%) and from re

299 his, we modelled the calling efficiencies of crickets within the full space of possible natural wing

300 Crickets would only consume beads when their mouth size