ライフサイエンスコーパス: sensory organ

1 we did not recognize any oral multicellular sensory organ.

2 al integrative structure known as the aboral sensory organ.

3 te for Merkel cell/neurite complexes in this sensory organ.

4 preclude analysis at the level of an entire sensory organ.

5 ing pathways may specify this highly derived sensory organ.

6 pes of air particle movements using a common sensory organ.

7 sues, including the skin, the body's largest sensory organ.

8 generates different cell types of the mature sensory organ.

9 rk that controls the development of a simple sensory organ.

10 namic turnover of cells in this regenerating sensory organ.

11 stitute the cellular components of the adult sensory organ.

12 egion, leading to animals lacking the apical sensory organ.

13 is highly expressed in the retina and other sensory organs.

14 tle patterns, and in the positioning of some sensory organs.

15 Perception involves motor control of sensory organs.

16 capitulate the spatial pattern of peripheral sensory organs.

17 TRPML3 in the inner ear as well as in other sensory organs.

18 it is needed for the wing margin, veins, and sensory organs.

19 inciples might apply to development of other sensory organs.

20 ne organogenesis, notably the development of sensory organs.

21 late gustatory signaling in these peripheral sensory organs.

22 le for the formation and subtype identity of sensory organs.

23 adhesion processes in maintaining the amphid sensory organs.

24 innervate only one of six to eight distinct sensory organs.

25 brain that process the input coming from the sensory organs.

26 hich contains multiple types of sex-specific sensory organs.

27 fiable phenotypes only in auditory or ocular sensory organs.

28 at normally control the development of these sensory organs.

29 sion of Msx1, a marker of certain vestibular sensory organs.

30 rtility and development of the eye, wing and sensory organs.

31 the eye and cause defects in other external sensory organs.

32 ndefined sites, including different types of sensory organs.

33 o determine the developmental origins of the sensory organs.

34 formation and zonal patterning of vestibular sensory organs.

35 nd generates the mirror-image pattern of the sensory organs.

36 ionship between hair and supporting cells in sensory organs.

37 mechanosensory circuits in combination with sensory organs.

38 nvolves sensory acquisition via the relevant sensory organs.

39 berrant mitoses, and reduced basal bodies in sensory organs.

40 time points of stimuli or their sampling by sensory organs.

41 velopment and are required for maturation of sensory organs.

42 d bigger LLP, affecting the final pattern of sensory organs.

43 connective tissues, whereas placodes produce sensory organs.

44 tion and cell fate determination of external sensory organs.

45 s requirement for the pigmentation of larval sensory organs.

46 mAnkrd6 causes PCP defects in the inner ear sensory organs.

47 information for their progression to mature sensory organs.

48 on of hair cell function within the auditory sensory organ, a mechanism thought to modulate the dynam

49 lan of the cephalopods with highly developed sensory organs, a complex central nervous system, and co

50 utants known to affect the function of these sensory organs also interfere with temperature synchroni

51 , a gene with a deeply conserved function in sensory organ and appendage development, in the sex comb

52 scheme, in which the interaction between the sensory organ and the environment is not affected by its

53 for the nematode, which utilizes specialized sensory organs and a chemoreceptor that is tuned to reco

54 The formation of the sensory organs and cells that make up the peripheral ner

55 nd functional alterations to both peripheral sensory organs and central brain regions.

56 ened head ectoderm that contribute to paired sensory organs and cranial ganglia.

57 atterned feed-forward excitation provided by sensory organs and experience drives the formation of ma

58 prediction based on a proposal that the ear sensory organs and fly mechanosensory organs are evoluti

59 (the common precursor region of many cranial sensory organs and ganglia), and other ectodermal domain

60 tant roles during the development of cranial sensory organs and ganglia, kidneys, hypaxial muscles an

61 to placodes and ultimately into many cranial sensory organs and ganglia.

62 from the dorsolateral ectoderm: chordotonal sensory organs and non-neural oenocytes.

63 They contribute to the paired sensory organs and the cranial sensory ganglia generatin

64 within the otic placode confers identity to sensory organs and to the corresponding otic neurons.

65 Inner ear sensory organs and VIIIth cranial ganglion neurons of th

66 mulation of EVs in the lumen of the cephalic sensory organ, and failure to release PKD-2::GFP-contain

67 piders is modified into extraordinarily long sensory organs (antenniform legs) covered with thousands

68 We propose that most Drosophila sensory organs are built from an archetypal lineage, and

69 Sensory organs are composed of neurons, which convert en

70 the levels of Scute are limiting, then some sensory organs are missing in achaete mutant flies.

71 Furthermore, aberrant and ectopic sensory organs are observed; most striking among these i

72 Sensory organs are often composed of neuronal sensory en

73 receptor neurons are silenced or when other sensory organs are severed, suggesting that increased sl

74 Sensory organs are specialized to detect and decode stim

75 Essential to the operation of these sensory organs are the biomineralized structures--otocon

76 Although the morphology and function of the sensory organs are well characterized, their origins and

77 Vertebrate sensory organs arise from epithelial thickenings called

78 These results suggest that a single sensory organ arises from cells in different parts of th

79 om the biological clock and from a metabolic sensory organ as the arcuate nucleus, are essential for

80 direct upstream regulators of Fgf10 in this sensory organ, as part of constructing the programme of

81 an brain could treat a tool like an extended sensory "organ." As with the body, participants localize

82 romast can break morphologic symmetry of the sensory organ at the stereocilia tips.

83 ls were killed and the peripheral vestibular sensory organs, brainstem, and cerebellum were collected

84 , ectopic scute expression produces external sensory organs but not chordotonal organs in the wing.

85 We show that neurons in a C. elegans sensory organ, called the amphid, undergo a collective d

86 cas show specific transformations in mechano-sensory organ cell identity, characteristic of mutations

87 correct specification of individual external sensory organ cells involves not only cut, but also the

88 trically localized in cells of the inner ear sensory organs, characteristic of components of conserve

89 L4) is thought to be the main route by which sensory organs communicate with cortex.

90 te signaling between cilia and glia to shape sensory organ compartments.

91 brain size reduction, because the brain and sensory organs complete their growth before the rest of

92 The Drosophila adult external sensory organ, comprising a neuron and its support cells

93 sec15(-) sensory organs contain extra neurons at the expense of s

94 Sensory organ damage induces a host of cellular and phys

95 he human SIFD syndrome, including anemia and sensory organ defects.

96 medial ventral ray, does not have increased sensory organ density, and we describe these findings in

97 Vertebrate craniofacial sensory organs derive from ectodermal placodes early in

98 nals, saccule, utricle, and their associated sensory organs, detects angular and linear acceleration

99 To understand the molecular basis of sensory organ development and disease, we have cloned an

100 that Drosophila Insensitive (Insv) promotes sensory organ development and has activity as a nuclear

101 acts peripherally to promote proprioceptive sensory organ development and the execution of specific

102 positively regulates Notch signaling during sensory organ development but acts negatively on Notch t

103 s localization, function, and how it impacts sensory organ development in vivo is not known.

104 Sensory organ development is also markedly disrupted in

105 d to affect asymmetric cell divisions during sensory organ development, carry lgl deletions that are

106 be upstream of very early events during the sensory organ development, hair cell differentiation and

107 into Wnt-responsive progenitor cells during sensory organ development.

108 with cell fate specification during eye and sensory organ development.

109 dy the basis of Eya1 dosage requirements for sensory organ development.

110 higher vertebrates has an additional role in sensory organ development.

111 t to inhibit Notch signaling and specify fly sensory organ development.

112 icular bristles on T3 at different points in sensory organ development.

113 enes involved in the constructive changes in sensory organ development.

114 In flies, overexpression of Atx-1 inhibits sensory-organ development by decreasing Senseless protei

115 DAF-6/patched-related site of action during sensory-organ development.

116 ndary, although their expression patterns in sensory organs differ.

117 sequent activation of Fgf signaling controls sensory organ differentiation, but not progenitor prolif

118 provide the first molecular evidence whereby sensory organs direct the development of the associated

119 In vertebrates, the inner ear sensory organs display distinctive forms of PCP.

120 cience but has not been adapted to the taste sensory organ due to anatomical constraint.

121 gene is widely expressed in placode-derived sensory organs during embryogenesis but Eya1 function ap

122 ES ion transport cells relative to inner ear sensory organs, dysplasia of the endolymph fluid space,

123 Here we report the discovery of a sensory organ embedded within the fibrous symphysis betw

124 The repair of sensory organs enables animals to continuously detect en

125 If sensory organs encode environment, this code must be dec

126 ation of either mechanosensory or structural sensory organ epithelia.

127 e role of the TSC in the Drosophila external sensory organ (ESO), a classic model of asymmetric cell

128 e C. elegans male tail constitute a compound sensory organ essential for mating.

129 ir-279/996 cluster, with a majority of notum sensory organs exhibiting transformation of sheath cells

130 Within these sensory organs, expression of the transcription factor E

131 the ancestral-like coding sequences rescued sensory organ fate in atonal mutants, in contrast to non

132 ner of a selector gene to control neural and sensory organ fate specification in the otocyst.

133 veloped mature nerve terminals and epidermal sensory organs first; also, in developing cortex, marker

134 The carotid body is a sensory organ for detecting arterial blood O2 levels and

135 cochlea and the vestibule, is a specialized sensory organ for hearing and balance.

136 Carotid bodies, the sensory organs for detecting arterial oxygen, express 5-

137 In Drosophila, candidate sensory organs for detecting the gravity vector were pre

138 e halteres of dipteran insects are essential sensory organs for flight control.

139 In chickens, the sensory organs for taste are the taste buds in the oral

140 ination and migration of neural cells during sensory organ formation in the spider.

141 ergize with proneural proteins and to induce sensory organ formation in vivo.

142 (OV), resulting in the failure of inner ear sensory organ formation, and in duplication of the cochl

143 neurogenesis and tissue specification during sensory organ formation.

144 al line placodes, which exhibit two modes of sensory organ formation: elongation to form sensory ridg

145 The Drosophila external sensory organ forms in a lineage elaborating from a sing

146 at glia are required for multiple aspects of sensory organ function.

147 e involved in patterning or specification of sensory organs, ganglion cells and hair cell mechanorece

148 Insect sensory organs have been a favorable model system for in

149 tic responsiveness highlight how the primary sensory organs have been optimized and can be modulated

150 ne cut is a hierarchal regulator of external sensory organ identity and is required to pattern the se

151 es a bony system supporting soft tissues and sensory organs implicated in either olfactory or thermor

152 In particular, the auditory sensory organ in the cochlea, adorned with precisely pat

153 aining isoforms and transforms the fate of a sensory organ in the male tail.

154 ion of the past 5 years is that very diverse sensory organs in Drosophila are produced by astonishing

155 correct identity of external (bristle-type) sensory organs in Drosophila.

156 and investigate its role in the formation of sensory organs in mammal and fish model organisms.

157 tions of taste cells in peripheral gustatory sensory organs in mice.

158 Animals actively move their sensory organs in order to acquire sensory information.

159 rate Gsk3-beta) regulates the development of sensory organs in the anterior-dorsal quadrant of the wi

160 ateral induction produces misshapen or fused sensory organs in the chick.

161 alised areas of ectoderm that contributed to sensory organs in the common ancestor of vertebrates and

162 The maintenance of taste sensory organs in the tongue was shown 140 years ago to

163 Specialized sensory organs in the vertebrate head originate from thi

164 Cranial placodes, which give rise to sensory organs in the vertebrate head, are important emb

165 and the self-organization of rosette-shaped sensory organs in the zebrafish lateral line system.

166 Our results indicate that in certain sensory organs, in which the requirement to transduce sp

167 This unique sensory organ includes taste buds, papilla epithelium an

168 focused on the nervous system and associated sensory organs including the olfactory organ, retina, le

169 region often gives rise to cells in multiple sensory organs, including cells that apparently disperse

170 Diverse sensory organs, including mammalian taste buds and insec

171 A widely-accepted assumption is that the sensory organ is the first station in a serial chain of

172 Input from the sensory organs is required to pattern neurons into topog

173 ce in the Drosophila melanogaster peripheral sensory organ lineage is controlled by the non-neuronall

174 proneural transcription factor Achaete, and sensory organ loss caused by Amun overexpression can be

175 While animals track or search for targets, sensory organs make small unexplained movements on top o

176 cal labial palpomeres with dense specialized sensory organs, match those of modern taxa and suggest t

177 per patterning of gene expression related to sensory organ morphogenesis (Otx1 and Bmp4, respectively

178 iption and the control of cell number during sensory organ morphogenesis.

179 ne primordium (pLLP) generates the zebrafish sensory organs (neuromasts, NMs).

180 In the head, terminal sensory organ neurons showed increased activity in respo

181 As plants have neither specialized sensory organs nor a nervous system, intercellular regul

182 The semicircular duct system is part of the sensory organ of balance and essential for navigation an

183 seous labyrinth, which houses the vestibular sensory organ of balance and orientation [4].

184 The main sensory organ of Caenorhabditis elegans, the amphid, pro

185 e ablated the sheath glial cell of the major sensory organ of Caenorhabditis elegans.

186 reparation of the rat vestibular crista, the sensory organ of the semicircular canals that sense head

187 derlie glial morphological plasticity in the sensory organs of C. elegans.

188 rophy, negatively regulates EV levels in the sensory organs of Caenorhabditis elegans in a cilia spec

189 ts among the cells that give rise to the ray sensory organs of Caenorhabditis elegans.

190 led serrano (sano) as being expressed in the sensory organs of Drosophila larvae.

191 mmetric cell divisions that give rise to the sensory organs of Drosophila melanogaster.

192 The sensory organs of the avian ear are able to regenerate h

193 The sensory organs of the Drosophila adult leg provide a sim

194 beta (TGF-beta) family, is expressed in all sensory organs of the frog inner ear, as it is in the de

195 ng axon, conveys information received by the sensory organs of the front contralateral leg to the neu

196 ion of SoxC genes in vivo results in stunted sensory organs of the inner ear and loss of hair cells.

197 The mechanisms of formation of the distinct sensory organs of the inner ear and the non-sensory doma

198 single sensory competent zone from which all sensory organs of the inner ear develop.

199 anation for regenerative differences between sensory organs of the inner ear, but shows that addition

200 Notably, vestibular sensory organs of the inner ear, the maculae, exhibit a

201 tic placode and otocyst can give rise to the sensory organs of the inner ear, though there were diffe

202 4 also guide the migration of germ cells and sensory organs of the lateral line.

203 re I show that crocodilians have specialized sensory organs on their faces that can detect small disr

204 a passive relay station of information from sensory organs or subcortical structures to the cortex.

205 nto the molecular mechanisms involved in leg sensory organ patterning, we have analyzed a Hedgehog (H

206 nosensory bristles, Delta (Dl) ligand in the sensory organ precursor (SOP) cell is targeted for ubiqu

207 he lateral inhibition process by which adult sensory organ precursor (SOP) cells are specified, but t

208 uring peripheral neurogenesis in Drosophila, sensory organ precursor (SOP) cells arise within proneur

209 increased production of sensory bristles and sensory organ precursor (SOP) cells on the notum of some

210 roneural gene specifies different numbers of sensory organ precursor (SOP) cells within distinct regi

211 l neurogenesis, Notch controls cell fates in sensory organ precursor (SOP) cells.

212 symmetric segregation of determinants in the sensory organ precursor (SOP) lineage.

213 During sensory organ precursor (SOP) specification, a single ce

214 From the PNC, a single cell, the sensory organ precursor (SOP), is selected as the adult

215 ise through asymmetric divisions of a single sensory organ precursor (SOP).

216 During Drosophila sensory organ precursor cell development, Numb segregate

217 In normal development, the sensory organ precursor cell divides asymmetrically thro

218 at this is indeed the case in the Drosophila sensory organ precursor cell lineage.

219 eby EGF secretion from a subset of abdominal sensory organ precursor cells (SOPs) to induce an approp

220 ling techniques to follow Notch receptors in sensory organ precursor cells in Drosophila.

221 embrane and reveal a novel morphology to the sensory organ precursor cells of wing imaginal discs.

222 In Drosophila sensory organ precursor cells, the localization of Numb

223 cell morphology, and the differentiation of sensory organ precursor cells.

224 REAM/MMB, DMyb promotes the PCD of specified sensory organ precursor daughter cells in at least two d

225 During sensory organ precursor divisions in Drosophila, the num

226 d is important for alpha-Ada function in the sensory organ precursor lineage, it was dispensable in t

227 mechanism), is restricted to anterior-dorsal sensory organ precursors (SOP) expressing Senseless (Sen

228 eural gene specifies a stereotypic number of sensory organ precursors (SOP) within each body segment

229 Sensory organ precursors (SOPs) also segregate Numb asym

230 In the developing wing disc, single sensory organ precursors (SOPs) are selected from proneu

231 Asymmetric division of sensory organ precursors (SOPs) in Drosophila generates

232 In Drosophila sensory organ precursors (SOPs), the core PCP components

233 ervous system leads to ectopic production of sensory organ precursors (SOPs), whereas overexpression

234 elix (bHLH) proneural proteins in Drosophila sensory organ precursors and is required for their norma

235 tial Hedgehog pathway activity in peripheral sensory organ precursors creates ORN populations with di

236 Strikingly, ectopic Insv fully rescued sensory organ precursors in Hairless null clones, indica

237 comprise the "proneural clusters" from which sensory organ precursors of the peripheral nervous syste

238 Hedgehog signaling in the imaginal sensory organ precursors thus confers differential ORN r

239 separate subareas, creating six of the eight sensory organs present in birds.

240 from the leg epithelium, rather than single sensory organ progenitors.

241 Peripheral sensory organs provide the first transformation of senso

242 by the information our eyes/retina and other sensory organs receive from the outside world, but stron

243 et the foundation for mechanistic studies of sensory organ regeneration and is crucial for identifyin

244 powerful paradigm to mechanistically dissect sensory organ regeneration.

245 od step toward physiological recovery during sensory-organ regeneration.

246 uer, in which glia and neurons of the amphid sensory organ remodel.

247 hat lumen formation in the C. elegans amphid sensory organ requires the gene daf-6.

248 Patterning of sensory organs requires precise regulation of neural ind

249 al and kinematic evidence indicate that this sensory organ responds to both the dynamic rotation of t

250 ersely Lmx1a (or cLmx1b in the chick) allows sensory organ segregation by antagonizing lateral induct

251 hterless are sufficient to generate thoracic sensory organs (SOs) in the absence of achaete-scute gen

252 The inner ear, which contains the sensory organs specialised for audition and balance, dev

253 The inner ear, which contains sensory organs specialized for hearing and balance, deve

254 In many sensory organs, specialized receptors are strategically

255 Among these, we identified a polycistronic, sensory organ-specific paralogous miRNA cluster that inc

256 We show that A2BP1 regulates sensory organ specification by potentiating Notch signal

257 , including eye patterning, wing margin, and sensory organ specification defects.

258 We find that Cut is required for wing-margin sensory organ specification in addition to and independe

259 ibition processes in the embryonic mesoderm, sensory organ specification in imaginal discs and cell t

260 cells of the proneural cluster orchestrates sensory organ specification.

261 s (much like numerosity maps) do not reflect sensory organ structure but instead emerge within the br

262 rovides the cerebral cortex with inputs from sensory organs, subcortical systems and the cortex itsel

263 Finally, the precursors of peripheral sensory organs such as the ear and olfactory placode und

264 The saccule is a vestibular sensory organ that depends upon regulation of its lumina

265 licated in O2 sensing by the carotid body, a sensory organ that monitors arterial blood O2 levels and

266 for the formation of muscle spindle fibers, sensory organs that are distinct from skeletal muscle co

267 the integration of motion cues from multiple sensory organs that individually do not provide an accur

268 ates, containing a group of mechanosensitive sensory organs that mediate hearing and balance.

269 ode into a labyrinth of chambers which house sensory organs that sense sound and are used to maintain

270 ues that are not represented directly in the sensory organ (the cochlea).

271 r duct houses both a vestibular and auditory sensory organ (the lagena macula and basilar papilla, re

272 The auditory sensory organ, the cochlea, not only detects but also ge

273 osensory lineage reconstruction of a complex sensory organ, the inner ear, by imaging zebrafish embry

274 region that gives rise to both the auditory sensory organ, the organ of Corti, and SG neurons.

275 The mammalian auditory sensory organ, the organ of Corti, consists of sensory h

276 fferentiation and patterning of the auditory sensory organ, the Usher complex, and the planar cell po

277 structural sexual dimorphism in a peripheral sensory organ, the VNO.

278 proposed a fundamental tradeoff between two sensory organs, the eye and the antenna.

279 of a neural prosthesis that can substitute a sensory organ: they bypass the malfunctioning auditory p

280 ied the olfactory Grueneberg ganglion as the sensory organ through which mammalian alarm pheromones s

281 coordinately oriented within each inner ear sensory organ to exhibit a particular form of planar cel

282 tures are the filopodia, which act like cell sensory organs to communicate with the extracellular mic

283 n supposed that microvilli on T cells act as sensory organs to enable search, but their strategy has

284 Neural pathways projecting from sensory organs to higher brain centers form topographic

285 map of neuronal projections from peripheral sensory organs to the brain.

286 e the environment through pathways that link sensory organs to the brain.

287 roup of migrating epithelial cells that form sensory organs, to understand how tissue growth is contr

288 st T cells, they can thus be considered as a sensory organ, trained on self-peptide-MHCs and primed t

289 Our sensory organs transduce errors in behavior.

290 The skin is our largest sensory organ, transmitting pain, temperature, itch, and

291 maintain coherent synaptic transmission from sensory organs undergoing frequent variations in the num

292 specifically in the socket cell of external sensory organs, via an autoregulatory enhancer called th

293 None of the other seven sensory organs was related to the ganglion neurons, sugg

294 As a model for a magnetic sensory organ we propose a system of radical pairs being

295 To decipher glial roles in sensory organs, we ablated the sheath glial cell of the

296 26b1 expression in the developing vestibular sensory organs, which generates the differential RA sign

297 es with Cut in the support cells of external sensory organs, which secrete the bristle shaft and sock

298 he development of the cranium and associated sensory organs, which were crucial for the evolution of

299 The whisker system is an important sensory organ with extensive neural representations in t

300 Contact of developing sensory organs with the external environment is establis