ライフサイエンスコーパス: compound eye

1 nterneurons from the ipsi- and contralateral compound eye.

2 site-dependent morphological changes in the compound eye.

3 y organs, conceivably with the function of a compound eye.

4 neighborhoods in the case of the Drosophila compound eye.

5 yme required specifically for patterning the compound eye.

6 eptor cells in each facet of the Drososphila compound eye.

7 igures ommatidial organisation in the mature compound eye.

8 nzyme required for patterning the developing compound eye.

9 re expressed in photoreceptor neurons in the compound eye.

10 phila, which lack the major opsin of the fly compound eye.

11 of the Drosophila central nervous system and compound eye.

12 affecting the development of the Drosophila compound eye.

13 cursor cells into ommatidial clusters in the compound eye.

14 with a specialized dorsal rim area in their compound eye.

15 second neuropil or medulla behind the fly's compound eye.

16 determine the shape and architecture of the compound eye.

17 in the fine visual acuity of the Drosophila compound eye.

18 for capturing light, within each facet of a compound eye.

19 , which form the new surface of the ruptured compound eye.

20 re mediated through different regions of the compound eye.

21 t brain that processes visual input from the compound eye.

22 spanning less than half of one facet of the compound eye.

23 s, regulates neuronal differentiation in the compound eye.

24 e field of view similar to that of a natural compound eye.

25 ics are studied in comparison with a natural compound eye.

26 ivision during development of the Drosophila compound eye.

27 pple arrays, to reduce reflectivity in their compound eyes.

28 ogenetically within several groups that lack compound eyes.

29 y reconstruct ancestral ostracods as lacking compound eyes.

30 ufficient to induce the formation of ectopic compound eyes.

31 from two optical sensors, the ocelli and the compound eyes.

32 adult brain and visual system, including the compound eyes.

33 rication of biologically inspired artificial compound eyes.

34 in, Arr1, in developing and adult Drosophila compound eyes.

35 In each facet of the Drosophila compound eye, a cluster of photoreceptor cells assumes a

36 vestigated how the adjacent primordia of the compound eye and dorsal head vertex are specified.

37 null allele and demonstrate that the mutant compound eye and larval visual system is not detectably

38 h rhodopsin-dependent light reception in the compound eye and photoreceptor cells in the Hofbauer-Buc

39 or cells in each of the ommatidia of the fly compound eye and the uniform orientation of the hairs in

40 sory systems including photoreceptors of the compound eyes and ocelli, large ocellar interneurons, an

41 expression of opsins in ostracod median and compound eyes and suggest that photoreceptor specific ex

42 an artificial eye inspired by superposition compound eyes and the retinal structure of elephantnose

43 ppearance corresponds with the appearance of compound eyes and walking legs.

44 e fly causes partial or complete loss of the compound eye, and this is associated with inappropriate

45 differentiation, ommatidia formation in the compound eye, and wing hair polarization.

46 The photoreceptors of the Drosophila compound eye are a classical model for studying cell fat

47 The photoreceptor cells of the Drosophila compound eye are precisely organized in elementary units

48 7 and R8 in the dorsal rim area (DRA) of the compound eye are specialized to detect the electric vect

49 Compound eyes are ideally suited for fast panoramic moti

50 Ipsi- and contralateral histaminergic compound eyes are required for photic entrainment.

51 One such debate is whether arthropod compound eyes are the product of single or multiple orig

52 ocopids--the only Ostracoda (Crustacea) with compound eyes--are nested phylogenetically within severa

53 rsoventral pattern is displayed in the adult compound eye as a distinct mirror symmetry across the do

54 ividual ommatidia, and the insulation of the compound eye as a whole.

55 Starfish have small compound eyes at the ends of their arms.

56 ces ectopic structures externally resembling compound eyes at the middorsal adult head of both basal

57 VS neuron to the ocellar axis closest to its compound eye axis.

58 e eyelets antagonize Cryptochrome (CRY)- and compound-eye-based photoreception in the large LNvs whil

59 e prototyped and characterized an artificial compound eye bearing a hemispherical field of view with

60 Patterning of the compound eye begins at the posterior edge of the eye ima

61 ods showed the external lattices of enormous compound eyes, but not the internal structures or anythi

62 In insects, compound eyes can have very different inner architecture

63 to assess functionality reveals that ectopic compound eyes can rescue the ability to respond to visua

64 In the adult Drosophila compound eye, color discrimination is achieved by UV-, b

65 C. chacei lacks the sophisticated compound eyes common to other decapod crustaceans.

66 receptor neurons (R cells) in the Drosophila compound eye connect to specific targets in the optic lo

67 sl result in extra R7 photoreceptors in the compound eye, consistent with overactivation of the rece

68 The Drosophila compound eye consists of approximately 750 independently

69 ificial ommatidium, like that of an insect's compound eyes, consists of a refractive polymer microlen

70 ceptor neurons (R1-R6, R7 and R8) in the fly compound eyes converges to the external part of the medu

71 la dachshund is necessary and sufficient for compound eye development and is required for normal leg

72 yes absent (eya) gene which is essential for compound eye development in Drosophila, was shown to be

73 eye development in Drosophila, and embryonic compound eye development in primitive insects.

74 The Drosophila compound eye develops by a complex series of cell intera

75 al strategies seem to be applicable to other compound eye devices, such as those inspired by moths an

76 tembryonic phase produces the adult specific compound eyes during late larval development and pupatio

77 a gracilis has a pair of bi-lobed apposition compound eyes, each with a large upward-looking portion

78 utive expression of TDP-43 in the Drosophila compound eye elicited widespread gene expression changes

79 this information in three axes, whereas the compound eyes encode in nine.

80 ese results illustrate exactly why arthropod compound eye evolution has remained controversial, becau

81 scribe a unique design method for biomimetic compound eyes featuring a panoramic, undistorted field o

82 receptor neurons (R cells) in the Drosophila compound eye form connections in different optic ganglia

83 functional units, at a cellular level, of a compound eye from the base of the Cambrian, more than ha

84 visual behaviours, a view that accords with compound eyes from the early Cambrian that were, in size

85 Visual transduction in the Drosophila compound eye functions through a pathway that couples rh

86 In the developing compound eye, glass function is regulated at two points:

87 tiple times in different arthropod groups or compound eyes have been lost in a seemingly inordinate n

88 the embryonic specification of the juvenile compound eye in directly developing insects while the Dr

89 Although the morphology of the compound eye in Drosophila and the single-chambered eye

90 scent of invertebrate structures such as the compound eye in Drosophila melanogaster.

91 -structural organization of the fiddler crab compound eye in relation to visual processing and visual

92 gene can trigger the development of ectopic compound eyes in flies.

93 Inspired by compound eyes in nature, these microlenses are designed

94 The Drosophila compound eye includes a dorsal domain specialized for th

95 The compound eye includes outer photoreceptors that express

96 eye induction-converges onto that of regular compound eyes, including up-regulation of several retina

97 logy of facets (ommatidia) in the Drosophila compound eye is accomplished by regulation of cell diffe

98 Development of the Drosophila melanogaster compound eye is also inhibited in flies that are mutant

99 Engineering a miniature artificial compound eye is challenging because it requires accurate

100 The Drosophila compound eye is formed by selective recruitment of undif

101 Patterning in the compound eye is fundamentally different: the boundary is

102 ocrystalline pattern of the adult Drosophila compound eye is generated by ordered selection of single

103 and R8 photoreceptor cells of the Drosophila compound eye is highly coordinated.

104 Although the fiddler crab compound eye is of the apposition type, typical for Brac

105 receptors in the ommatidia of the Drosophila compound eye is polarized, having a handedness or chiral

106 The Drosophila compound eye is specified by the concerted action of sev

107 vent in patterning the developing Drosophila compound eye is the progressive restriction of the trans

108 Although development of the adult Drosophila compound eye is very well understood, little is known ab

109 The acuity of compound eyes is determined by interommatidial angles, o

110 itz, a signal for ommatidial assembly in the compound eye, is transported to retinal axon termini in

111 petence to ectopically generate a functional compound eye-like structure.

112 Compound eye-loss, however, was provoked when ey and toy

113 amined to find that the red pigment from the compound eye masks much of the signal from biogenic amin

114 ernal structures or anything about how those compound eyes may have functioned.

115 Drosophila DUB essential for patterning the compound eye, might have a novel regulatory function; Fa

116 y of the antireflection properties of insect compound eyes, new examples of natural antireflective co

117 ise to numerous adult tissues, including the compound eyes, ocelli, antennae, maxillary palps and sur

118 the three-dimensional structure of the huge compound eye of a 160-million-year-old thylacocephalan a

119 We show here that the compound eye of both mosquitoes is divided into specific

120 The developing compound eye of Drosophila has long been a model of choi

121 The compound eye of Drosophila melanogaster is configured by

122 During the development of the compound eye of Drosophila several signaling pathways ex

123 e in establishing epithelial polarity in the compound eye of Drosophila.

124 m in a sequential fashion, in the developing compound eye of Drosophila.

125 honey-comb organization of ommatidia in the compound eye of insects.

126 Expression of the dMyc mutants in the compound eye of the adult fly results in a visible defec

127 ctural organization of the ommatidium in the compound eye of the fiddler crab, Uca vomeris, at both t

128 se chain reaction cloning, we found that the compound eye of Vanessa cardui has the typical ultrastru

129 t exceptionally preserved non-biomineralized compound eyes of a non-trilobite arthropod Cindarella eu

130 ence of refractive lenses in the complex and compound eyes of many invertebrates, relatively little i

131 lution better than this is not attainable in compound eyes of realistic size.

132 plysia, a sea hare), in jellyfish and in the compound eyes of some arthropods; all are different and

133 Here we study scaling in the compound eyes of workers of the wood ant, Formica rufa,

134 imposing the "neurocrystalline" order of the compound eye on the postsynaptic target field.

135 predation, many species have evolved unique compound eyes on the radioles that function as shadow or

136 r and is equipped with two separate pairs of compound eyes, one pair viewing above and one viewing be

137 e internal structures of a modern apposition compound eye open important insights into the evolution

138 d to interpreting external features, such as compound eyes or sensilla decorating appendages, and ear

139 indicating that the neurotransmitter of the compound eyes participates in both entrainment pathways.

140 In the developing Drosophila compound eye, pattern formation and cell-type specificat

141 egant automatic-gain control was revealed in compound eye photoreceptors: In bright light, an assembl

142 In the Drosophila compound eye, photoreceptors (R cells) that respond to l

143 The prototyped artificial compound eye possesses several characteristics similar t

144 input pathway, together with input from the compound eyes, precisely times the activity of flies und

145 ctly developing insects while the Drosophila compound eye primordium is evolutionarily related to the

146 In the compound eye, prospero (pros) is transcribed specificall

147 ngth-selective behaviors are mediated by the compound eye's narrow-spectrum photoreceptors R7 and R8

148 ttered1 (shtd1) mutation disrupts Drosophila compound eye structure.

149 The apposition type of compound eye that bees and other diurnal insects possess

150 by "chunks," unlike the conventional insect compound eye that decomposes the visual image in a point

151 dramatically enlarged eye-imaginal discs and compound eyes that are normally patterned.

152 icon-based focal plane arrays and artificial compound eyes that have hemisphere-like structures.

153 In the Drosophila compound eye the dorsal and ventral fields of eye units

154 of honey bees upon visual stimulation of the compound eye to analyze chromatic response properties.

155 of photoreceptor cells in each facet of the compound eye to eight.

156 markedly reorganizes the architecture of the compound eyes to resemble an open system.

157 e establishment of polarity within the adult compound eye via a mechanism that includes the four join

158 tic density, both in the ocellar pathway and compound eye visual neurons.

159 eurons and in ommatidial degeneration of the compound eye, which is rescued by expression of human PI

160 existence of neural arrangements serving the compound eyes, which are organized like neuropils servin

161 n most animal species, vision is mediated by compound eyes, which offer lower resolution than vertebr

162 Bythograea thermydron possess image-forming compound eyes with a visual pigment sensitive to the blu

163 Either compound eyes with detailed similarities evolved multipl

164 speed of the ocelli with the accuracy of the compound eyes without compromising either.