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1 e field of view similar to that of a natural compound eye.
2 ics are studied in comparison with a natural compound eye.
3 sual system commonly is considered to be the compound eye.
4 ivision during development of the Drosophila compound eye.
5  site-dependent morphological changes in the compound eye.
6 y organs, conceivably with the function of a compound eye.
7  neighborhoods in the case of the Drosophila compound eye.
8 yme required specifically for patterning the compound eye.
9 eptor cells in each facet of the Drososphila compound eye.
10 igures ommatidial organisation in the mature compound eye.
11 nzyme required for patterning the developing compound eye.
12 re expressed in photoreceptor neurons in the compound eye.
13 phila, which lack the major opsin of the fly compound eye.
14 of the Drosophila central nervous system and compound eye.
15  affecting the development of the Drosophila compound eye.
16 cursor cells into ommatidial clusters in the compound eye.
17 , which form the new surface of the ruptured compound eye.
18 idium, which is the basic visual unit of the compound eye.
19  spanning less than half of one facet of the compound eye.
20 nterneurons from the ipsi- and contralateral compound eye.
21  with a specialized dorsal rim area in their compound eye.
22  second neuropil or medulla behind the fly's compound eye.
23 the R8 photoreceptor array in the Drosophila compound eye.
24  determine the shape and architecture of the compound eye.
25  in the fine visual acuity of the Drosophila compound eye.
26  for capturing light, within each facet of a compound eye.
27 re mediated through different regions of the compound eye.
28 t brain that processes visual input from the compound eye.
29 s, regulates neuronal differentiation in the compound eye.
30 in, Arr1, in developing and adult Drosophila compound eyes.
31 pple arrays, to reduce reflectivity in their compound eyes.
32 ogenetically within several groups that lack compound eyes.
33 y reconstruct ancestral ostracods as lacking compound eyes.
34 ufficient to induce the formation of ectopic compound eyes.
35  have inspired the development of artificial compound eyes.
36 ng maneuver is initiated by their ocelli and compound eyes.
37 in mutant clones causes defects in wings and compound eyes.
38 ion system and in dissociated ommatidia from compound eyes.
39 a dramatic transformation of the ocelli into compound eyes.
40 from two optical sensors, the ocelli and the compound eyes.
41 adult brain and visual system, including the compound eyes.
42 rication of biologically inspired artificial compound eyes.
43 heir retinas under the stable lenses of each compound eye(1-3).
44              In each facet of the Drosophila compound eye, a cluster of photoreceptor cells assumes a
45                           We reconstruct its compound eye and analyze the optical properties of the o
46 vestigated how the adjacent primordia of the compound eye and dorsal head vertex are specified.
47  null allele and demonstrate that the mutant compound eye and larval visual system is not detectably
48 h rhodopsin-dependent light reception in the compound eye and photoreceptor cells in the Hofbauer-Buc
49 rigger a transformation of the ocelli into a compound eye and the neighboring head epidermis into an
50 or cells in each of the ommatidia of the fly compound eye and the uniform orientation of the hairs in
51 ness independently of visual function in the compound eye and without affecting circadian rhythms.
52 Drosophila melanogaster, including a pair of compound eyes and a trio of simple eyes called ocelli.
53 ts' visual system by covering one of the two compound eyes and analyzed their ability to recognize fa
54 y of adaptations is found among animals with compound eyes and even closely related taxa can show var
55 sory systems including photoreceptors of the compound eyes and ocelli, large ocellar interneurons, an
56 work are differentially expressed within the compound eyes and ocelli.
57                    Arthropods have intricate compound eyes and optic neuropils, exhibiting exceptiona
58 fer new insights into the miniaturization of compound eyes and scaling of sensory organs in general.
59  expression of opsins in ostracod median and compound eyes and suggest that photoreceptor specific ex
60  an artificial eye inspired by superposition compound eyes and the retinal structure of elephantnose
61 ppearance corresponds with the appearance of compound eyes and walking legs.
62 e fly causes partial or complete loss of the compound eye, and this is associated with inappropriate
63  differentiation, ommatidia formation in the compound eye, and wing hair polarization.
64 thropods typically possess two types of eyes-compound eyes, and the ocellar, so called 'median eyes'.
65                                         This compound-eye architecture could be a useful model for op
66             Strategies that aim to mimic the compound-eye architecture involve integrating photodetec
67 h as insects and crustaceans is based on the compound-eye architecture, consisting of a dense array o
68         The photoreceptors of the Drosophila compound eye are a classical model for studying cell fat
69    The photoreceptor cells of the Drosophila compound eye are precisely organized in elementary units
70 7 and R8 in the dorsal rim area (DRA) of the compound eye are specialized to detect the electric vect
71                                          The compound eyes are crucial for such visual navigation; ho
72                                       Insect compound eyes are easily recognizable despite dramatic d
73                                              Compound eyes are ideally suited for fast panoramic moti
74                                        While compound eyes are in focus of many investigations, media
75        Ipsi- and contralateral histaminergic compound eyes are required for photic entrainment.
76         One such debate is whether arthropod compound eyes are the product of single or multiple orig
77 ocopids--the only Ostracoda (Crustacea) with compound eyes--are nested phylogenetically within severa
78 rsoventral pattern is displayed in the adult compound eye as a distinct mirror symmetry across the do
79 ividual ommatidia, and the insulation of the compound eye as a whole.
80                          Starfish have small compound eyes at the ends of their arms.
81 ces ectopic structures externally resembling compound eyes at the middorsal adult head of both basal
82 VS neuron to the ocellar axis closest to its compound eye axis.
83 e eyelets antagonize Cryptochrome (CRY)- and compound-eye-based photoreception in the large LNvs whil
84 e prototyped and characterized an artificial compound eye bearing a hemispherical field of view with
85                            Patterning of the compound eye begins at the posterior edge of the eye ima
86 ods showed the external lattices of enormous compound eyes, but not the internal structures or anythi
87 om a different region compared to the insect compound eyes calling organ homology into question.
88                    We developed a biomimetic compound eye camera with an effective pixel number of 4.
89                                  In insects, compound eyes can have very different inner architecture
90  research questions (e.g. how low resolution compound eyes can localise small objects) using modern m
91 to assess functionality reveals that ectopic compound eyes can rescue the ability to respond to visua
92                      In the adult Drosophila compound eye, color discrimination is achieved by UV-, b
93            C. chacei lacks the sophisticated compound eyes common to other decapod crustaceans.
94 with a fully modern type of visual system, a compound eye comparable to that of living bees, dragonfl
95 receptor neurons (R cells) in the Drosophila compound eye connect to specific targets in the optic lo
96  sl result in extra R7 photoreceptors in the compound eye, consistent with overactivation of the rece
97                               The Drosophila compound eye consists of approximately 750 independently
98 ificial ommatidium, like that of an insect's compound eyes, consists of a refractive polymer microlen
99 the almost anucleate brain, all cells of the compound eye contain nuclei.
100 ceptor neurons (R1-R6, R7 and R8) in the fly compound eyes converges to the external part of the medu
101               The new fossil preserves large compound eyes, delicate mouthparts, and even gills.
102 la dachshund is necessary and sufficient for compound eye development and is required for normal leg
103 yes absent (eya) gene which is essential for compound eye development in Drosophila, was shown to be
104 eye development in Drosophila, and embryonic compound eye development in primitive insects.
105 ehog (Hh) and Decapentaplegic (Dpp) initiate compound eye development, while reciprocal domains of Dp
106                               The Drosophila compound eye develops by a complex series of cell intera
107 al strategies seem to be applicable to other compound eye devices, such as those inspired by moths an
108 tembryonic phase produces the adult specific compound eyes during late larval development and pupatio
109 a gracilis has a pair of bi-lobed apposition compound eyes, each with a large upward-looking portion
110 utive expression of TDP-43 in the Drosophila compound eye elicited widespread gene expression changes
111  this information in three axes, whereas the compound eyes encode in nine.
112 ese results illustrate exactly why arthropod compound eye evolution has remained controversial, becau
113 e the primordial visual system, and that the compound eyes evolved later.
114     Here, we present a biomimetic apposition compound eye fabricated using a microfluidic-assisted 3D
115 y scans to map the viewing directions of all compound eye facets, and found a non-uniform sampling of
116 scribe a unique design method for biomimetic compound eyes featuring a panoramic, undistorted field o
117 receptor neurons (R cells) in the Drosophila compound eye form connections in different optic ganglia
118  functional units, at a cellular level, of a compound eye from the base of the Cambrian, more than ha
119  visual behaviours, a view that accords with compound eyes from the early Cambrian that were, in size
120 different cell types of the retina in insect compound eyes, fulfill important functions.
121        Visual transduction in the Drosophila compound eye functions through a pathway that couples rh
122                            In the developing compound eye, glass function is regulated at two points:
123 tiple times in different arthropod groups or compound eyes have been lost in a seemingly inordinate n
124  the embryonic specification of the juvenile compound eye in directly developing insects while the Dr
125               Although the morphology of the compound eye in Drosophila and the single-chambered eye
126 scent of invertebrate structures such as the compound eye in Drosophila melanogaster.
127 -structural organization of the fiddler crab compound eye in relation to visual processing and visual
128 nging from tiny pigment-cup eyes in limpets, compound eyes in ark clams and pinhole eyes in Nautilus,
129                             The structure of compound eyes in arthropods has been the subject of many
130 ensional vision via multi-view geometry like compound eyes in flies, or time-of-flight sensing like e
131  gene can trigger the development of ectopic compound eyes in flies.
132                                  Inspired by compound eyes in nature, these microlenses are designed
133 ions into the visual abilities of apposition compound eyes in the deep sea.
134 ed here, comprehensive models for apposition compound eyes in the mesopelagic, the dominant eye form
135                               The Drosophila compound eye includes a dorsal domain specialized for th
136                                          The compound eye includes outer photoreceptors that express
137 eye induction-converges onto that of regular compound eyes, including up-regulation of several retina
138 s the outermost ommatidial pigment shield in compound eyes incorporating a chitinous cornea.
139 logy of facets (ommatidia) in the Drosophila compound eye is accomplished by regulation of cell diffe
140   Development of the Drosophila melanogaster compound eye is also inhibited in flies that are mutant
141                               The Drosophila compound eye is an attractive system for unraveling how
142           Engineering a miniature artificial compound eye is challenging because it requires accurate
143                               The Drosophila compound eye is formed by selective recruitment of undif
144                            Patterning in the compound eye is fundamentally different: the boundary is
145 ocrystalline pattern of the adult Drosophila compound eye is generated by ordered selection of single
146 and R8 photoreceptor cells of the Drosophila compound eye is highly coordinated.
147                    Although the fiddler crab compound eye is of the apposition type, typical for Brac
148 receptors in the ommatidia of the Drosophila compound eye is polarized, having a handedness or chiral
149                               The Drosophila compound eye is specified by the concerted action of sev
150 vent in patterning the developing Drosophila compound eye is the progressive restriction of the trans
151 Although development of the adult Drosophila compound eye is very well understood, little is known ab
152                                The acuity of compound eyes is determined by interommatidial angles, o
153                 Revealing the functioning of compound eyes is of interest to biologists and engineers
154 itz, a signal for ommatidial assembly in the compound eye, is transported to retinal axon termini in
155 petence to ectopically generate a functional compound eye-like structure.
156                                              Compound eye-loss, however, was provoked when ey and toy
157 amined to find that the red pigment from the compound eye masks much of the signal from biogenic amin
158 ernal structures or anything about how those compound eyes may have functioned.
159  Drosophila DUB essential for patterning the compound eye, might have a novel regulatory function; Fa
160                                    To date, 'compound eye models' (CEMs) have largely explored featur
161                                   Drosophila compound eye morphogenesis transforms a simple epitheliu
162 y of the antireflection properties of insect compound eyes, new examples of natural antireflective co
163 tories that will eventually develop into the compound eye, ocelli, head epidermis, bristles, antenna
164 ise to numerous adult tissues, including the compound eyes, ocelli, antennae, maxillary palps and sur
165  the three-dimensional structure of the huge compound eye of a 160-million-year-old thylacocephalan a
166 llently preserved internal structures of the compound eye of a 429 Mya old Silurian trilobite, Aulaco
167 n to visualize six ommatidial classes in the compound eye of a lycaenid butterfly with a four-opsin v
168  The first complete 3D reconstruction of the compound eye of a minute wasp species sheds light on the
169 t cellular-level reconstruction of the whole compound eye of an insect, the miniaturized parasitoid w
170                        We show here that the compound eye of both mosquitoes is divided into specific
171                                          The compound eye of cockroaches is obligatory for entrainmen
172                               The developing compound eye of Drosophila has long been a model of choi
173                                          The compound eye of Drosophila melanogaster is configured by
174                During the development of the compound eye of Drosophila several signaling pathways ex
175 e in establishing epithelial polarity in the compound eye of Drosophila.
176 m in a sequential fashion, in the developing compound eye of Drosophila.
177  honey-comb organization of ommatidia in the compound eye of insects.
178        Expression of the dMyc mutants in the compound eye of the adult fly results in a visible defec
179                                          The compound eye of the female M. viggianii consists of 29 o
180 ctural organization of the ommatidium in the compound eye of the fiddler crab, Uca vomeris, at both t
181 se chain reaction cloning, we found that the compound eye of Vanessa cardui has the typical ultrastru
182 t exceptionally preserved non-biomineralized compound eyes of a non-trilobite arthropod Cindarella eu
183 ence of refractive lenses in the complex and compound eyes of many invertebrates, relatively little i
184      By applying our model to the apposition compound eyes of Phronima, a mesopelagic hyperiid amphip
185 lution better than this is not attainable in compound eyes of realistic size.
186 plysia, a sea hare), in jellyfish and in the compound eyes of some arthropods; all are different and
187                 Here we study scaling in the compound eyes of workers of the wood ant, Formica rufa,
188 imposing the "neurocrystalline" order of the compound eye on the postsynaptic target field.
189  predation, many species have evolved unique compound eyes on the radioles that function as shadow or
190 r and is equipped with two separate pairs of compound eyes, one pair viewing above and one viewing be
191 e internal structures of a modern apposition compound eye open important insights into the evolution
192 d to interpreting external features, such as compound eyes or sensilla decorating appendages, and ear
193  indicating that the neurotransmitter of the compound eyes participates in both entrainment pathways.
194                 In the developing Drosophila compound eye, pattern formation and cell-type specificat
195                            Long UV-sensitive compound eye photoreceptor neurons terminated in medulla
196 egant automatic-gain control was revealed in compound eye photoreceptors: In bright light, an assembl
197                            In the Drosophila compound eye, photoreceptors (R cells) that respond to l
198 estalks typifying crown Malacostraca provide compound eyes populated by ommatidia revealing structure
199                    The prototyped artificial compound eye possesses several characteristics similar t
200  input pathway, together with input from the compound eyes, precisely times the activity of flies und
201 ctly developing insects while the Drosophila compound eye primordium is evolutionarily related to the
202                                       In the compound eye, prospero (pros) is transcribed specificall
203 directions is determined mainly by the fly's compound eye, revealing the intimate connections between
204 ngth-selective behaviors are mediated by the compound eye's narrow-spectrum photoreceptors R7 and R8
205    Here we show that the organization of the compound eye shapes the systematic variation in the pref
206 eyeless/Pax6 expression cause differences in compound eye size within and between Drosophila species.
207 ttered1 (shtd1) mutation disrupts Drosophila compound eye structure.
208 green-sensitive photoreceptor neurons of the compound eye terminated in lamina layers LA1 and LA2, ad
209                       The apposition type of compound eye that bees and other diurnal insects possess
210  by "chunks," unlike the conventional insect compound eye that decomposes the visual image in a point
211 dramatically enlarged eye-imaginal discs and compound eyes that are normally patterned.
212  are mediated via visual feedback from their compound eyes that detect retinal slip, as well as rapid
213 icon-based focal plane arrays and artificial compound eyes that have hemisphere-like structures.
214                            In the Drosophila compound eye the dorsal and ventral fields of eye units
215 a biomimetic analogue to naturally occurring compound eyes, the eye's full-colour 3D to 2D mapping ca
216 of honey bees upon visual stimulation of the compound eye to analyze chromatic response properties.
217  of photoreceptor cells in each facet of the compound eye to eight.
218 markedly reorganizes the architecture of the compound eyes to resemble an open system.
219 e establishment of polarity within the adult compound eye via a mechanism that includes the four join
220 tic density, both in the ocellar pathway and compound eye visual neurons.
221                             A unique bifocal compound eye visual system found in the now extinct tril
222                 Inspired by the desert ants' compound eyes, we developed a single-shot pol-PD based o
223 l configurations regularly appear in the fly compound eye, which is connected to the visual center by
224 eurons and in ommatidial degeneration of the compound eye, which is rescued by expression of human PI
225 existence of neural arrangements serving the compound eyes, which are organized like neuropils servin
226 n most animal species, vision is mediated by compound eyes, which offer lower resolution than vertebr
227  Bythograea thermydron possess image-forming compound eyes with a visual pigment sensitive to the blu
228                                       Either compound eyes with detailed similarities evolved multipl
229 ion, arthropods have developed sophisticated compound eyes with extraordinary visual capabilities tha
230                            Most animals have compound eyes, with tens to thousands of lenses attached
231 speed of the ocelli with the accuracy of the compound eyes without compromising either.

 
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