ライフサイエンスコーパス: cricket

1 produces neurons throughout the life of the cricket.

2 generated sound in a sonorously stridulating cricket.

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

4 rrespond to regional grouping of conspecific crickets.

5 related within eastern North American field crickets.

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

7 milar to those produced by female lebinthine crickets.

8 ed between, species to explore speciation in crickets.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

24 Mormon crickets and juvenile locusts form huge migratory bands-

25 Crickets and other orthopteran insects sense air current

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

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

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

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

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

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

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

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

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

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

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

37 The cricket auditory system has to deal with highly stereoty

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 Tree crickets differ sharply from this scheme.

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

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

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

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

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

58 Crickets fed NP CeO2-exposed zucchini leaves contained s

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

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

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

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

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

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

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

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

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

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

69 coustic preference variation in the Hawaiian cricket genus Laupala.

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

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

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

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

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

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

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

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

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

79 entally induced seasonal environments in the cricket Gryllus bimaculatus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 520 mum, to pinpoint the 5 kHz chirp of its cricket host.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 The dicistrovirus Cricket Paralysis virus contains a unique dicistronic RN

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

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

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

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

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

129 The cricket paralysis virus internal ribosome entry site (Cr

130 The cricket paralysis virus internal ribosome entry site (IR

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

132 Using the cricket paralysis virus internal ribosome entry site ele

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

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

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

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

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

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

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

140 ated viruses, encephalomyocarditis virus and cricket paralysis virus.

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

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

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

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

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

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

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

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

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

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

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

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

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

154 ation phylogeny for this pair of hybridizing cricket species.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 Crickets use their long antennae as tactile sensors.

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

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

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

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

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

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