ライフサイエンスコーパス: antennae

1 ndografts, incorporating MRI receiver coils (antennae).

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

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

4 ene expression is disrupted in black-painted antennae.

5 ynthetic energy transfer in light-harvesting antennae.

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

7 e molecular mechanism and that reside in the antennae.

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

9 erent sensilla types on Cx. quinquefasciatus antennae.

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

11 are dependent on the integrity of the larval antennae.

12 me based on their biased expression in drone antennae.

13 synthesis of cyanobacterial light-harvesting antennae.

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

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

16 ordium resulting in the induction of ectopic antennae.

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

18 antitatively bearing LDN structures on their antennae.

19 ons of legs with reduced tiptop develop like antennae.

20 present in the trimers of the photosystem II antennae.

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

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

23 ining proteins as the major light-harvesting antennae.

24 circadian olfactory responses in Drosophila antennae.

25 pendages, respectively, to be transformed to antennae.

26 thoracic and abdominal) segments to develop antennae.

27 g transformation of mandibular appendages to antennae.

28 ring chlorophyll to nascent photosystems and antennae.

29 preferentially in the olfactory organs, the antennae.

30 phyll b and phycobilisomes as photosynthetic antennae.

31 compartment has been demonstrated in legs or antennae.

32 utgrowths of wing tissue from eyes, legs and antennae.

33 y (Fucalpha1-2Galbeta1-4(Fucalpha1-3)GlcNAc) antennae.

34 adiative (heat) dissipation of energy in the antennae.

35 ctly within the light-collecting chlorophyll antennae.

36 onformational change on the resulting branch antennae.

37 displacement, and angular displacement than antennae.

38 pass dependent upon a circadian clock in the antennae.

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

40 ngth and number of olfactory sensilla on the antennae.

41 creasing thermal dissipation at the level of antennae.

42 ive long sensilla trichodea of male silkmoth antennae.

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

44 e sampling movements with their unrestrained antennae.

45 s, containing reaction centers and connected antennae.

46 cit stereotyped leg movements that groom the antennae.

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

48 onstitutes a previously unknown role for the antennae.

49 erlap brain segments and supply the eyes and antennae.

50 of mechanosensory fibers originating in the antennae.

51 ulses and measuring sensory responses in the antennae.

52 these clusters to serve as light-harvesting antennae.

53 rom olfactory sensory neurons located on the antennae.

54 as electrodes, catalysts, interconnects and antennae.

55 d thus maintains the olfactory acuity of the antennae.

56 e second highest expression levels in female antennae.

57 mes more cuticular hydrocarbons than groomed antennae.

58 stribution of the remaining antenna for both antennae 6 and 6'.

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

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

61 Moreover, nongroomed antennae accumulated significantly more environmental co

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

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

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

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

66 ere activated after touch stimulation of the antennae and before initiation of escape.

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

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

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

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

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

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

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

74 or-evoked afferent activity in both isolated antennae and intact preparations.

75 In Drosophila melanogaster, antennae and legs are homologous structures that differ

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

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

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

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

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

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

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

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

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

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

86 , with MsNOS expressed at high levels in the antennae and the MsGCs expressed at high levels in a sub

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

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

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

90 n be triggered by tactile stimulation of the antennae, and it is then independent of the giant intern

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

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

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

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

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

96 sensory cells of the antennae, even when the antennae are excised and maintained in isolated organ cu

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

98 The antennae are important for the inclination compass becau

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

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

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

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

103 Mosquito antennae are very sensitive acoustic receivers, featurin

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

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

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

107 Crickets use their long antennae as tactile sensors.

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

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

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

111 sion and can induce the formation of ectopic antennae at novel locations in the body, including the h

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

113 a; (c) PV-1 is N-glycosylated and its glycan antennae bear terminal nonreducing galactosyl residues i

114 involved in photosynthetic light harvesting antennae biogenesis.

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

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

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

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

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

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

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

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

123 In several of the pLH1 antennae, carotenoid depletion contributed to the phenot

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

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

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

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

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

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

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

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

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

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

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

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

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

137 xpression occur in chemosensory cells of the antennae, even when the antennae are excised and maintai

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

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

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

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

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

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

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

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

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

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

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

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

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

151 d sialyl-N-acetyllactosamine oligosaccharide antennae from biantennary glycans using MS3, and the loc

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

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

154 ore fucosylation while its absence signifies antennae fucosylation.

155 Nanoplasmonic optical antennae, functioning as biosensors to significantly enh

156 Nanoplasmonic optical antennae, functioning as nanoplasmonic gene switches to

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

187 The antennae of flying moths vibrate and experience Coriolis

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

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

190 e involved in sex pheromone reception by the antennae of male moths.

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

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

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

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

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

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

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

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

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

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

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

202 The glycan antennae of the surface-adsorbed glycoproteins apparentl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

217 Antennae providing similar luminescence intensities with

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

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

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

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

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

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

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

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

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

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

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

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

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

231 ressed in the head and the cardia, crop, and antennae-structures related to feeding.

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

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

234 jority of neurons from wild-type but not eag antennae, suggesting that Eag may have a dendritic local

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

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

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

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

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

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

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

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

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

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

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

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

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

248 The antennae thus play a crucial role in maintaining flight

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

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

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

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

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

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

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

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

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

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

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

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

261 rough the hydrophilic sensillum lymph in the antennae toward their membrane receptors remains the ini

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

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

264 osialylated as the presence of fucose on the antennae was found to suppress the addition of extra sia

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

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

267 NeuAc alpha2-3 substituted Galbeta1-4GlcNAc antennae were common.

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

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

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

271 acent to the electrically inactive receiving antennae were measured.

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

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

274 Antennae were stimulated with forces approximating those

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

276 ere disruption of adult structures; legs and antennae were truncated and eye formation was suppressed

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

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

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

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

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

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

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

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

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

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