ライフサイエンスコーパス: antennae

1 ndografts, incorporating MRI receiver coils (antennae).

2 elocity cues at the sensitive mechanosensory antennae.

3 male reproductive organs but retained female antennae.

4 s, containing reaction centers and connected antennae.

5 cit stereotyped leg movements that groom the antennae.

6 ncy, but not to the tonic deflections of the antennae.

7 onstitutes a previously unknown role for the antennae.

8 erlap brain segments and supply the eyes and antennae.

9 ulses and measuring sensory responses in the antennae.

10 these clusters to serve as light-harvesting antennae.

11 rom olfactory sensory neurons located on the antennae.

12 as electrodes, catalysts, interconnects and antennae.

13 d thus maintains the olfactory acuity of the antennae.

14 e second highest expression levels in female antennae.

15 mes more cuticular hydrocarbons than groomed antennae.

16 and from air (geranyl acetate) than groomed antennae.

17 e in light-entrained circadian clocks in the antennae.

18 ene expression is disrupted in black-painted antennae.

19 ynthetic energy transfer in light-harvesting antennae.

20 bution of energy from the core back onto the antennae.

21 e molecular mechanism and that reside in the antennae.

22 ht tones in the vibrations of the mosquito's antennae.

23 erent sensilla types on Cx. quinquefasciatus antennae.

24 ith a peak around the middle of the night in antennae.

25 are dependent on the integrity of the larval antennae.

26 me based on their biased expression in drone antennae.

27 synthesis of cyanobacterial light-harvesting antennae.

28 pheromone-detecting sensilla on B. mori male antennae.

29 ordium resulting in the induction of ectopic antennae.

30 n of female pheromones: the legs, wings, and antennae.

31 antitatively bearing LDN structures on their antennae.

32 ons of legs with reduced tiptop develop like antennae.

33 present in the trimers of the photosystem II antennae.

34 all and joints and as auditory organs in the antennae.

35 ining proteins as the major light-harvesting antennae.

36 circadian olfactory responses in Drosophila antennae.

37 pendages, respectively, to be transformed to antennae.

38 thoracic and abdominal) segments to develop antennae.

39 d to various parts of the body including the antennae.

40 ction), 40 hrs APF (neurogenesis), and adult antennae.

41 of mechanosensory fibers originating in the antennae.

42 ty of the transformation taking place in the antennae.

43 d most of them occur in equal numbers on the antennae.

44 displacement, and angular displacement than antennae.

45 pass dependent upon a circadian clock in the antennae.

46 cated in the brain and a moon compass in the antennae.

47 ngth and number of olfactory sensilla on the antennae.

48 creasing thermal dissipation at the level of antennae.

49 ive long sensilla trichodea of male silkmoth antennae.

50 OBP5) are highly abundant in male and female antennae.

51 e sampling movements with their unrestrained antennae.

52 g of Scr, transform the labial appendages to antennae, a result seen in the other insects only when b

53 mbrane surfaces can act as proton-collecting antennae, accelerating proton uptake by membrane-bound p

54 Moreover, nongroomed antennae accumulated significantly more environmental co

55 ts showed that over a 24-h period nongroomed antennae accumulated three to four times more cuticular

56 , because residual female pheromone on their antennae adapted their peripheral sensilla and habituate

57 emale pheromone that contaminated the male's antennae also elicited courtship from other non-contamin

58 cond (deutocerebral) head segment, including antennae and 'great appendages' of Cambrian arthropods,

59 lattices that morph into frequency-shifting antennae and a human face, demonstrating functionality a

60 otoresponsive polymers thus serve jointly as antennae and actuators that reversibly respond to distin

61 hese interactions, we used lectins to screen antennae and antennal lobes at different stages of adult

62 ly measured circadian gene expression in the antennae and brain of T. saltator and show the clock gen

63 to hierarchically organize light-harvesting antennae and catalytic centers to achieve solar energy c

64 The other is a roachoid with long antennae and chewing mouthparts very similar in form to

65 eans, including differentiated tritocerebral antennae and epipodite-bearing biramous trunk appendages

66 rdotonal neurons detect displacements of the antennae and excite three different classes of functiona

67 in affinities, and preserves portions of the antennae and eyes, coupled with a heavily spined habitus

68 alized to discrete neurons within the larval antennae and facilitate odor-evoked responses in Xenopus

69 at electric fields cause deflections in both antennae and hairs.

70 sis in various extraocular tissues including antennae and legs.

71 ctively removed female pheromone from males' antennae and maintained their chemosensory acuity and se

72 Ablation of the antennae and maxillary palps reduced, but did not elimin

73 These neurons project from the antennae and maxillary palps to the antennal lobe (AL) a

74 stigate two putative electric field sensors: antennae and mechanosensory hairs.

75 ected findings pose a novel function for the antennae and open a new line of investigation into clock

76 Thus, grooming of the antennae and other sensory appendages is an important st

77 in male tarsi and could be also detected in antennae and palpi of both sexes, while CjapOBP2, beside

78 Regulation of the interactions between antennae and photosystems allows photosynthetic organism

79 depended upon mechanosensory inputs from the antennae and proprioceptive feedback from the ipsilatera

80 A shallow equilibrium between the antennae and reaction center in photosystem II will cert

81 , is applied to determine how photosynthetic antennae and reaction centers are activated in the groun

82 urons" that integrate signals across the two antennae and receive input from at least three classes o

83 BPx are expressed at very high levels in the antennae and so could be involved in olfaction.

84 odern termitophiles, with concealed head and antennae and strong posteriorly directed abdominal setae

85 an air piston and experimentally manipulated antennae and visual feedback.

86 gaster were compared with those of wild-type antennae and wild-type legs by means of degeneration and

87 n isolated based on transformations of adult antennae and/or legs toward palps.

88 ram (EAG) recordings revealed that A. cerana antennae are 10-fold more sensitive to GOL than to other

89 Movements of single antennae are ambiguous with respect to wind direction, b

90 Silver nanorice antennae are coupled with a patterned gold triangle nano

91 Light-harvesting antennae are critical for collecting energy from sunligh

92 Furthermore, the spalt/spalt-related null antennae are defective in hearing.

93 al light-harvesting systems, the chlorosomal antennae are devoid of a protein scaffold to orient the

94 Large antennae are disadvantageous at low light intensities be

95 wo strategies for installation of sialylated antennae are explored, and both approaches converge on a

96 The antennae are important for the inclination compass becau

97 Here, we show that the antennae are necessary for proper time-compensated Sun c

98 Key fragment ions revealed that these antennae are predominantly found on the upper 6-arm of t

99 ple-output' communications, because multiple antennae are required to access the polarization or spat

100 The olfactory antennae are separated by a fraction of a millimeter, an

101 Mosquito antennae are very sensitive acoustic receivers, featurin

102 Appendages, such as limbs, fins and antennae, are structures common to many animal body plan

103 rs and the light-harvesting phycobiliprotein antennae arise from the oxygen-dependent ring opening of

104 Mosquitoes use their antennae as hearing organs to locate and interact with o

105 Crickets use their long antennae as tactile sensors.

106 on centers, rather than the PSII chlorophyll antennae, as a major site of (1)O(2) accumulation in pla

107 orientation of T. saltator is located in the antennae, as is the case for Monarch butterflies.

108 As a result, when an odour activates the antennae asymmetrically, ipsilateral central neurons beg

109 ll numbers of ORNs in the Anopheles mosquito antennae at low concentrations.

110 Additionally, ablating ant antennae at the onset of pupation results in AL defects

111 ands bearing distant hydroxycoumarin-derived antennae attached through triazole linkers were modest s

112 involved in photosynthetic light harvesting antennae biogenesis.

113 Flies also sense air motion with their antennae, but how this is used in flight control is unkn

114 sduces suggests that cilia may not be static antennae, but organelles whose functions are shaped by t

115 uencing of ApolPDE, isolated from day 2 male antennae by multiple chromatographic steps, led to cDNA

116 fications of photosynthetic light harvesting antennae called phycobilisomes that occur during complem

117 th a pair of abdominal appendages resembling antennae, called cerci.

118 the different ways in which light-harvesting antennae can be regulated in mesophilic and thermophilic

119 We show how light-harvesting antennae can be tuned to maximize power conversion effic

120 unnatural alpha-Gal and beta-Man terminating antennae can sequentially be decaged by an appropriate g

121 tosensitizers and construct light-harvesting antennae capable of achieving panchromatic absorption an

122 cells (2 inhibitory, 1 excitatory), two were antennae cells (1 inhibitory, 1 excitatory), one was an

123 icipate in energy transfer from the proximal antennae complexes (CP43 and CP47) to the RC core chromo

124 ures can be decorated with novel fucosylated antennae composed of Fucalpha(1-3)GlcNAc.

125 ructured substance accumulated on nongroomed antennae, covering sensillar pores, but not on groomed a

126 data suggest these organelles are cellular "antennae" critically required to modulate ALNP behavior.

127 ield and functioning of the light-harvesting antennae decreased simultaneously, indicating that photo

128 Nerves from uniramous antennae define the deutocerebrum, and a stout pair of m

129 Removing or painting the antennae did not affect daily activity rhythms or compet

130 Extracellular recordings from the antennae do not show any electrophysiological correlates

131 However, how flying insects move their antennae during active turns and how such movements migh

132 ongly aligned with the directions of sensory antennae (e.g. copepods); and this is certain to influen

133 imers present in a variety of photosynthetic antennae, efficient vibration-assisted energy transfer i

134 Natural light-harvesting antennae employ a dense array of chromophores to optimiz

135 of very short duration, as occur when their antennae encounter narrow filaments in an odor plume.

136 oscillations were measured in photosynthetic antennae excited by sequences of coherent ultrashort las

137 ize of neighboring morphological structures (antennae, eyes, or wings, depending on the location of t

138 For two divergently regulated LHCF antennae family mRNAs, in vivo 4-thiouracil metabolic la

139 in architectures with both distant and close antennae for all of the Lns.

140 onic nanostructures are known to act as tiny antennae for efficiently focusing the electromagnetic fi

141 implying the existence of proton collecting antennae for expedited proton transport.

142 nts in dual-functional nanoplasmonic optical antennae for label-free biosensors and nanoplasmonic gen

143 ge the composition of their light-harvesting antennae for maximal absorption of different wavelengths

144 al of using the new compounds as fluorescent antennae for molecular imaging, spectroscopy, microscopy

145 to probe the characteristics of such QDs as antennae for photosensitized release of bioactive agents

146 d to possess chlorosomes as light-harvesting antennae for phototrophic growth.

147 LSC) utilizing two pi-conjugated polymers as antennae for small amounts of the valued perylene bisimi

148 this indicated that the accessibility of the antennae for the molecular targets C4b and C3b was not a

149 Chlorosomes are unique light-harvesting antennae found in two phyla of green bacteria: Chlorobi

150 crotubule-based organelles that project like antennae from the surface of most cells in the body.

151 Primary cilia extend like antennae from the surface of most eukaryotic cells into

152 ore fucosylation while its absence signifies antennae fucosylation.

153 Nanoplasmonic optical antennae, functioning as biosensors to significantly enh

154 Nanoplasmonic optical antennae, functioning as nanoplasmonic gene switches to

155 nt for both pb and Scr give rise to complete antennae, further demonstrating appendage homology.

156 dynamics in photosynthetic light-harvesting antennae has motivated many theoretical models exploring

157 strong chewing mouthparts, robust and short antennae having long setae, legs with only one single ta

158 (workers, male and female alates), tissues (antennae, head, thorax, and abdomen), and developmental

159 Creative designs of nanoplasmonic optical antennae (i.e. plasmon resonant nanoparticles) have beco

160 sual motion, Drosophila actively moved their antennae in a direction opposite to that of the visual m

161 ts of Johnston's organs at the base of their antennae in a frequency range characteristic of the Cori

162 Tribolium labial appendages also develop as antennae in double mutants.

163 iran great appendages and that the sensorial antennae in Mandibulata derived from ancestral raptorial

164 he best-fit models showed that the two mCrry antennae in mCrry-Ig were extended from the Fc fragment.

165 ease in the proportion of uncoupled proximal antennae in PSII as a function of increasing growth ligh

166 y cyanobacteria alter their light-harvesting antennae in response to changes in ambient light-color c

167 epeating structural building blocks of these antennae in Saturniid moths.

168 Photosystems associate with antennae in vivo to increase the size of photosynthetic

169 Mechanical deflections of both hairs and antennae increase with the electric charge carried by th

170 The semiporous, multiscale nature of these antennae influences how odor molecules reach their surfa

171 tunnels allow for effective limb, body, and antennae interaction with walls, which facilitate rapid

172 ctromagnetic energy radiated from cell phone antennae into ex vivo brain tissue.

173 eous activation of multiple straight or loop antennae is a potentially promising technique for rapid

174 The array of nano-antennae is fabricated on a lapped section of standard t

175 sexes, the number of 9-exon ORs expressed in antennae is tightly correlated with the number of glomer

176 ry receptor neurons (ORNs) in the Drosophila antennae, is poorly understood.

177 clock neurons, or the photoreceptors, or the antennae, is sufficient to mediate negative geotaxis and

178 n profiles as they relate to sensory tissue (antennae, legs, and mouthparts), sex (male and female),

179 In Drosophila melanogaster, the antennae, legs, genitalia, and analia make up a serially

180 e membranes, including the primary cilium-an antennae-like structure on the luminal side of the colle

181 EmaA monomers trimerize to form antennae-like structures on the surface of the bacterium

182 cantly higher in dyads using only their left antennae (LL) than it was in those using only their righ

183 the shrimp such as pleopods, pereopods, and antennae located at near-surface layers (undetected by p

184 issues, including the compound eyes, ocelli, antennae, maxillary palps and surrounding head capsule.

185 laneta nub-RNAi first nymphs develop crooked antennae, no visible changes are observed in the morphol

186 Like all arthropod appendages, antennae not only supply sensory information but may als

187 ide MOFs and by using the organic linkers as antennae, novel smart materials can be developed, acting

188 d on the abdomen, wings, legs, proboscis and antennae of adult honey bees.

189 The antennae of adult male German cockroaches detect a conta

190 the functional state of the light harvesting antennae of both photosystem I and II of these plants is

191 compensatory responses in the composition of antennae of both photosystems.

192 were uniquely or primarily expressed in the antennae of both sexes, suggesting their putative role i

193 Collectively, our data show that the antennae of complex N-glycans serve to protect the V3 lo

194 by olfactory receptor neurons (ORNs) on the antennae of Culex pipiens quinquefasciatus (Cx. quinquef

195 ants and the phycobiliprotein photosynthetic antennae of cyanobacteria, red algae, and cryptomonads.

196 The antennae of flying moths vibrate and experience Coriolis

197 re expressed at extremely high levels in the antennae of insects, and have long been believed essenti

198 mone-binding proteins (PBPs), present in the antennae of male moth and other insect species, bind the

199 omone-binding proteins (PBPs) located in the antennae of male moth species play an important role in

200 roduced an Illumina-based transcriptome from antennae of males and females as well as neonate head ti

201 urons located in T1 trichoid sensilla on the antennae of males and females.

202 e to show that glucuronic acid is present on antennae of plasma glycoproteins underlying the correspo

203 ompounds elicited physiological responses in antennae of pollinating Desmometopa flies.

204 ransfer and trapping in the light harvesting antennae of purple photosynthetic bacteria is an ultrafa

205 The antennae of R. prolixus showed increased expression of s

206 Some bear pectinate antennae of remarkable architecture thought to improve o

207 one-degrading enzyme, PjapPDE, from >100,000 antennae of the Japanese beetle.

208 Light-harvesting antennae of the LHC family form transmembrane three-heli

209 induce electrophysiological responses in the antennae of the model springtail Folsomia candida, which

210 the maxillary palps of mosquitoes and in the antennae of the more genetically tractable fruitfly, Dro

211 ests that a cytochrome P450 specific to male antennae of the pale-brown chafer, Phyllopertha diversa,

212 covering sensillar pores, but not on groomed antennae of the same individuals.

213 The glycan antennae of the surface-adsorbed glycoproteins apparentl

214 ted GlcAbeta1--> 3Galbeta1-->4GlcNAcbeta1--> antennae, of which those containing sulfated GlcA, depic

215 ophila melanogaster following the removal of antennae or other sensory tissues.

216 ves the loss of appendages (legs, chelipeds, antennae or tails, for example), skin autotomy can occur

217 hite-cane, nocturnal insects and mammals use antennae or whiskers for near-range orientation.

218 ompartments, such as olfactory cilia, insect antennae, or even synaptic boutons.

219 ling the composition of its light-harvesting antennae, or phycobilisomes, in response to changes in t

220 ngulation between transmitting and receiving antennae (parallel = 90 degrees C +/- 9 degrees C; 45 de

221 This suggests that the BChl a antennae, photosynthetic reaction centers, and remaining

222 d excitation energy is transferred among the antennae pigments and converted into chemical energy at

223 pcb genes encoding constitutive PSI and PSII antennae, plus one PSI iron-regulated pcb gene, whereas

224 re the largest and one of the most efficient antennae produced by chlorophototrophic organisms.

225 uired during photosynthetic light-harvesting antennae production, such as occurs during complementary

226 hrobilin chromophores, which are attached to antennae proteins called phycoerythrins.

227 ular mechanism, and those that reside in the antennae provide time compensation.

228 noreactivity in chemosensory hairs of female antennae provides evidence in support of the participati

229 Antennae providing similar luminescence intensities with

230 d motile cilia/flagella function as cellular antennae, receiving signals from the environment and sub

231 ve long been considered as 'sensory cellular antennae', responding as chemo-sensors, mechano-sensors

232 , a sex pheromone receptor expressed in male antennae, responds strongly to E11 but also generally to

233 he ionotropic receptor family the largest of antennae-rich olfactory genes, second only to odorant re

234 sed in all tissues examined, that CYP6AT1 is antennae-rich, and that CYP4AW1 is antennae-specific.

235 than it was in those using only their right antennae (RR).

236 erogeneity of synthetic analogues of natural antennae-self-assembled molecular nanotubes-by two compl

237 all differences in odor concentration across antennae separated by less than 1 mm [1], and a single o

238 , we show that mechanosensory input from the antennae serves a similar role during flight in hawk mot

239 Furthermore, spalt/spalt-related mutant antennae show severe reductions in Johnston's organ, the

240 the individual (high Chl:C(max), i.e., high antennae size) conflicts with artificial selection of a

241 time compensated by circadian clocks in the antennae so that fall migrants can maintain a fixed flig

242 have isolated, cloned, and expressed a male antennae-specific pheromone-degrading enzyme (PDE) [Anth

243 YP6AT1 is antennae-rich, and that CYP4AW1 is antennae-specific.

244 al linkage information, unambiguously define antennae substitutions, and differentiate isomeric glyco

245 Nature's highly efficient light-harvesting antennae, such as those found in green sulfur bacteria,

246 rhythms and orientation of sandhoppers with antennae surgically removed, or unilaterally occluded wi

247 l drumming (AD), wherein a female trills her antennae synchronously on the rims of nest cells while f

248 from turbulent water currents or wind using antennae that bear chemosensory hairs.

249 Chlorosomes are light-harvesting antennae that enable exceptionally efficient light energ

250 We propose that polysomes may act as antennae that enhance the rates of capture of the limite

251 Males of long-horned bees bear antennae that exceed body length.

252 ew appreciation of primary cilia as cellular antennae that sense a wide variety of signals could help

253 Cilia serve as cellular antennae that translate sensory information into physiol

254 sillum recordings supported this hypothesis: antennae that were prevented from being groomed were sig

255 g that although SiOBPs were expressed in the antennae, the major regions of expression were in the he

256 three CSPs are highly expressed in the adult antennae, the olfactory organ of insects.

257 s energy at the site of the light-harvesting antennae, the phycobilisomes.

258 of the major photosynthetic light-harvesting antennae, the phycobilisomes.

259 the conventional puffing of stimulus on the antennae, the receptor responded to bombykol but not to

260 The antennae thus play a crucial role in maintaining flight

261 ionotropic receptors were enriched in female antennae, thus making the ionotropic receptor family the

262 as experienced during forward flight, causes antennae to actively move forward as a sigmoidal functio

263 troscopic information on single multipigment antennae to be recorded in a nonperturbative aqueous env

264 surface of eukaryotic cells, act as cellular antennae to detect and transmit signals from the extrace

265 nd guidewires that incorporated MRI receiver antennae to enhance device visibility.

266 Nature has chosen chlorophylls in plants as antennae to harvest light for the conversion of solar en

267 brain that relays odor information from the antennae to higher brain centers.

268 orresponding front-to-back optic flow causes antennae to move backward, as a linear function of relat

269 that walking flies combine signals from both antennae to orient to wind during olfactory search behav

270 rom the activation of sensory neurons in the antennae to the excitation of descending neurons in the

271 e significantly less responsive than groomed antennae to the sex pheromone component periplanone-B, a

272 lor the properties of their light-harvesting antennae to the spectral distribution of ambient light.

273 (DTPA)-monoamide ligands bearing molecular "antennae" to enhance metal fluorescence via intramolecul

274 alities, including mechanoreceptors on their antennae, to stabilize the direction and speed of flight

275 llation suggests that these light-harvesting antennae trade energy reversibly between the protein and

276 ycans, despite these lacking the fucosylated antennae typical of many other eukaryotes; some of these

277 nvestigated the morphology of antennules and antennae using fluorescence and scanning electron micros

278 No preferred orientation of the antennae was identified, and this indicated that the acc

279 inspired by the olfactory sensilla of insect antennae, we show that coating nanopores with a fluid li

280 he expression levels of genes transcribed in antennae were compared between 5(th) instar larvae, and

281 -specific olfactory receptor neurons in male antennae were completely desensitized by direct applicat

282 hesized these compounds and showed that male antennae were highly sensitive to them.

283 acent to the electrically inactive receiving antennae were measured.

284 f a single sialic acid on biantennary glycan antennae were resolved.

285 r the [M+3H](3+) ions observed as the glycan antennae were shortened by stepwise exoglycosidase treat

286 Antennae were stimulated with forces approximating those

287 III)) complexes with coumarin or carbostyril antennae were synthesized and their photophysical proper

288 entre that is surrounded by light-harvesting antennae, which absorb the light and transfer the excita

289 ined by their unusually large photosynthetic antennae, which are among the largest ever recorded in m

290 lines plays analogous roles in developing antennae, which are serially homologous to legs, suggest

291 o pairs of very long biramous antennules and antennae, which are used both for attracting client fish

292 Mosquitoes hear with their antennae, which in most species are sexually dimorphic.

293 highly rhythmic in brains and clear-painted antennae, while rhythmic clock gene expression is disrup

294 ing device consists of an array of gold nano-antennae with a total length of 2.3 cm that generate cou

295 through rapid interaction of appendages and antennae with tunnel walls to jam the falls.

296 Eucera males have elongated antennae, with 10 times more pore plates and three times

297 Cilia act as cellular sensory antennae, with defects resulting in human ciliopathies.

298 re sharper than the mechanical tuning of the antennae, with males being more sensitive than females.

299 orant-binding protein genes were enriched in antennae, with the other half being predominantly expres

300 excess native cuticular hydrocarbons on the antennae would impair olfactory reception.