ライフサイエンスコーパス: tentacle

1 tor that can be extended into a microrobotic tentacle.

2 re identified in L22; one mapped outside the tentacle.

3 t new mutations mapped in L4, all within the tentacle.

4 en attached only via its mobile beta-subunit tentacle.

5 orms as well as the mutant lacking the alpha tentacle.

6 tentacle zone and hypostome, but not in the tentacles.

7 e sensory cells in the ectoderm covering its tentacles.

8 of putative nitrergic sensory neurons in its tentacles.

9 is particularly high in the endoderm of the tentacles.

10 s present as far apically as the base of the tentacles.

11 irmed by comparative study of squid arms and tentacles.

12 ere able to trigger the growth of additional tentacles.

13 bsence of nerve cells in the endoderm of the tentacles.

14 eton with evidence of simple, densely packed tentacles.

15 uniform distribution of a variable number of tentacles.

16 sis correlate with shaping of the elongating tentacles.

17 with the sole alpha-helices representing the tentacles.

18 around the L protein in a manner similar to tentacles.

19 ar, although disproportionately broad, lacks tentacles.

20 y affects the epithelial cells that form the tentacles.

21 4,000/mm2), and TSCs in the tips of cephalic tentacles (100/mm2).

22 the time it took an anemone to re-extend its tentacles after a threatening stimulus, and immersion re

23 mersion response time, the time to re-extend tentacles after simulated tidal immersion.

24 n unexpected increase in the number of their tentacles, allowing for the possibility that these neopl

25 CP with either tentacle alone can cap, as can the isolated beta tentacl

26 acle alone can cap, as can the isolated beta tentacle alone, suggesting that the individual tentacles

27 (b) Neural processes in tentacles along the rows of "boxes" providing structural

28 Behavioral data indicate that tentacle and proboscis movements are controlled by a sha

29 5-HT-IR was observed in neuropil of tentacle and rhinophore ganglia with many transverse 5-H

30 system, and acidic glands, nor in peripheral tentacle and rhinophore ganglia.

31 complex behaviors such as torsion of a squid tentacle and the bending behavior of octopus arms or ele

32 Morphological analyses of the tentacles and adjacent mouthparts in pollinators and clo

33 as been claimed that these worms have collar tentacles and blend morphological features of the two ma

34 es, gonads, respiratory trees, hemal system, tentacles and body wall.

35 uscular specializations such as the anterior tentacles and the posterior sucker that are used as soon

36 beta subunits of CP are mobile extensions ("tentacles"), and these regions are responsible for high-

37 The sensory epithelium of rhinophores, tentacles, and mouth showed a highly structured glomerul

38 y organs (ASO: pairs of rhinophores and oral tentacles, and the anterior field formed by the oral pla

39 The ctene rows, apical organ, and tentacle apparatus are complex structures that are gener

40 ors and closely related taxa showed that the tentacle appears abruptly in female pollinating yucca mo

41 The highest density of ISCs is in the oral tentacles (approximately 1,200/mm2), SSCs in the middle

42 Uncovered in the ectoderm of feeding tentacles are conventional type I hair cells and previou

43 d in vitro, we show that the tips of the PFD tentacles are required to form binary complexes with aut

44 ar behaviors: cytoskeleton is deformed, cell tentacles are significantly shortened, and cell migratio

45 ed by a tentacle to its mouth by bending the tentacle around a joint formed by stiffened distal and p

46 protein can be localized not only to ECM of tentacles as we previously reported, but also to endoder

47 fectly tapered fossil leaves end in a single tentacle, as in both modern Roridula species.

48 This spiraling tentacle-based grabbing modality, the direct peeling-ena

49 ead regeneration and transdifferentiation of tentacle battery cells.

50 her siphonophores, and also suggest that the tentacle bearing zooids should be called tentacular palp

51 sues include an extendable, gullwing-shaped, tentacle-bearing organ surrounding a central mouth, whic

52 mely the tentacle-less enteropneusts and the tentacle-bearing pterobranchs.

53 ructurally unique, cytoplasmic fibrils whose tentacles bind and regulate asymmetric traffic.

54 ino acids of the alpha-subunit, the proposed tentacle, bound to S100B as a free synthetic peptide or

55 and is transcriptionally patterned into four tentacle buds.

56 nt of several organs, including the pharynx, tentacle bulbs and apical organ.

57 ous anatomical novelties, including arms and tentacles, but little is known about the developmental m

58 and NO3- were present at high levels in the tentacles, but were not detectable in NADPH-d-negative a

59 Also, supernumerary tentacles, by permitting higher foraging efficiency for

60 The tentacles carry pinnules, each with a row of stiff filam

61 Loss of both tentacles causes a complete loss of capping activity.

62 that during a local withdrawal reflex of the tentacle, CC5 is necessary and sufficient for the unilat

63 re subsequently retrieved from a C. fleckeri tentacle cDNA library.

64 atically analyze the venom components of the tentacles, column, and mesenterial filaments of sea anem

65 and peptide precursors were identified from tentacles, column, and mesenterial filaments respectivel

66 scribe the formation of the embryonic mouth, tentacles, combs, aboral organ, and putative sensory cel

67 pore, located adjacent to a horseshoe-shaped tentacle complex.

68 spired by marine creatures that present long tentacles containing multiple adhesive domains to effect

69 The alpha tentacle contributes more to capping affinity and kineti

70 stingly, in the intermediate pulsation phase tentacles could pulsate individually without synchroniza

71 protease inhibitor (SmCI) isolated from the tentacle crown of the annelid Sabellastarte magnifica.

72 undamental processes contribute to embryonic tentacle development in the cnidarian Nematostella vecte

73 se findings show an unexpected plasticity of tentacle development, and link post-embryonic body patte

74 The tentacles differ in key aspects from those seen in lopho

75 is tested by simulating extension of a squid tentacle during prey capture; our numerical predictions

76 The ether tentacles (E = methoxymethyl) allow these cations to eff

77 The composite interwoven by CNT tentacle enhances conductivity and prevents the restacki

78 proboscis, and the tentacle suggest that the tentacle evolved quickly through expression of the genet

79 A weak touch to a tentacle excites the ipsilateral PAS and evokes a local

80 The resulting micro-tentacle exhibit spiraling with the final radius as smal

81 sory areas (the mouth area, rhinophores, and tentacles) express the most intense staining, primarily

82 nal region is proposed to act as a flexible "tentacle," extending away from the body of capping prote

83 These snakes are fully aquatic and use tentacles for passive detection of nearby fish.

84 Cephalopods tentacles, for example, can undergo multiple trajectorie

85 The gene plays a role in tentacle formation and in patterning the lower end of th

86 ical defects, as observed during budding and tentacle formation in Hydra, and stabilize aster/vortex-

87 ys a role in the specification of tissue for tentacle formation.

88 anipulations indicate the gene has a role in tentacle formation.

89 ith Hym-301 dsRNA resulted in a reduction of tentacles formed as the head developed during bud format

90 ide resulted in an increase in the number of tentacles formed, while treatment with Hym-301 dsRNA res

91 cifically in the regulation of the number of tentacles formed.

92 : a) Measured 29 morphological characters of tentacles from 45 siphonophore species, b) mapped these

93 long helices extend from a central body like tentacles from a jellyfish.

94 ermediate domains of HslU, which extend like tentacles from the hexameric ring formed by the amino-te

95 hanism, thus no new mechanism was needed for tentacle function.

96 e body column to the extracellular milieu in tentacles further suggests that HMP-1 is a secreted prot

97 only in a few neurons of the rhinophore and tentacle ganglia.

98 ult of rhythmic opening and closing of their tentacles, has fascinated scientists since the 18th cent

99 The regions where the tentacle helices attach to the body of the Tim8-Tim13 co

100 o expansion segments, which contain extended tentacles in metazoans.

101 To learn more about the roles of the tentacles in ribosome assembly and function, we isolated

102 In addition, we find no evidence of tentacles in the available deep-sea photographs (publish

103 the specialized sensory function of bivalve tentacles in the common jingle shell, Anomia simplex.

104 nd delivers them preferentially among DTPs' "tentacles" in the SA-DTP system to produce strong, ampli

105 uctures such as stolons and nematocyst-laden tentacles, induced to deter encroachment by competitors,

106 rents respond to water movements and project tentacle information to the tectum in alignment with vis

107 ntacle alone, suggesting that the individual tentacles interact with more than one actin subunit at a

108 Finally, we observe that the NELF-A tentacle interacts with the RPB2 protrusion and is neces

109 s not observed nearby when the single apical tentacle is formed.

110 The observed order of tentacles is a real-world example of an optimal hashing

111 sensitivity of the rhinophores than the oral tentacles, led us to conclude that the two pairs of chem

112 two main hemichordate body plans, namely the tentacle-less enteropneusts and the tentacle-bearing pte

113 We identify tentacle-like helices and a globular complex capping the

114 visualize the distal tip cell which extends tentacle-like processes that directly contact distal ger

115 tional phases exclusive to eukaryotes led to tentacle-like rRNA expansions.

116 sion segments (ESs) consist of multitudes of tentacle-like rRNA structures extending from the core ri

117 itself appear at the regenerating tip, with tentacle markers displaced to the region below.

118 We tested the tentacle model in vitro with recombinant mutant CPs.

119 C terminus is not mobile as predicted by the tentacle model.

120 xhibit a unique, rhythmic pulsation of their tentacles (Movie S1), first noted by Lamarck nearly 200

121 oint formed by stiffened distal and proximal tentacle muscles, and thus may use motor control strateg

122 Commissural tracts and tentacle nerves branching off the connectives appear lat

123 e arrangement and developmental order of the tentacles obey a mathematical rule.

124 biological muscular hydrostats such as squid tentacles, octopus arms and elephant trunks.

125 the basic patch near the joint of the alpha tentacle of CP shown previously to drive most of the ass

126 Here we show that the terminus of an rRNA tentacle of Homo sapiens contains 10 tandem G-tracts tha

127 At first glance, the trailing tentacles of a jellyfish appear to be randomly arranged.

128 core is exposed to water, like the extended tentacles of Actinia, and adsorbs the dissolved contamin

129 ed end, block interaction between C-terminal tentacles of capping protein and filament end-sides, and

130 Mutations in the tentacles of L4 and L22 confer macrolide resistance in a

131 Branches of the connectives innervate the tentacles of the head and the sucker organ in the tail.

132 cerebral, pedal, and buccal ganglia; in the tentacles of the oral hood; in the sensory end of the rh

133 Here we utilize the tentacles of the sea anemone Nematostella vectensis as a

134 snap traps of Venus flytraps and catapulting tentacles of the sundew Drosera glanduligera.

135 Inspired by the "tentacles" of an octopus, herein, we present a framework

136 ven 'jellyfish' galaxies-galaxies with long 'tentacles' of material that extend for dozens of kilopar

137 The actin-binding COOH-terminal region, the "tentacle," of the CP beta subunit was important for bind

138 eproductive system, followed by rhinophores, tentacles, oral veil, mouth, buccal mass, and esophagus.

139 show aggressive responses to eversion of the tentacle organs of the caterpillars.

140 promoters, we examined how DAC-2-25 affects tentacle patterning.

141 gene is not necessary for the formation of a tentacle per se.

142 b (Fgfrb) signaling in ring muscles defines tentacle primordia in fed polyps.

143 rowth is observed in polyp but not embryonic tentacle primordia.

144 Tentacle probes (TPs) have a hairpin structure similar t

145 labeled probes, molecular beacons (MBs) and tentacle probes (TPs).

146 yzing over 1000 growing polyps, we find that tentacle progression is stereotyped and occurs in a feed

147 mer resembles a jellyfish with alpha-helical tentacles protruding from a beta barrel body defining a

148 pening and overlapping muscle fibers between tentacles, providing the mechanisms for tentacle synchro

149 d release would create a homology-searching "tentacle." Rec8 and Red1/Mek1 also independently license

150 In contrast, removal of the beta tentacle reduced the affinity by only 300-fold and did n

151 Given that prolonged tentacle retraction reduces foraging opportunities and c

152 HT-IR cell bodies were not observed in foot, tentacles, rhinophores, oral veil, mouth, buccal mass, e

153 The NADPH-d-reactive neurons in the tentacles send processes to regions adjacent to the inne

154 significant affinity, to the proposed alpha-tentacle sequence of whole native capping protein in sol

155 tions in P. sibogae; i.e., ISCs and the oral tentacles serve contact- or short-distance chemoreceptio

156 conclude that the two pairs of chemosensory tentacles serve different chemosensory functions in P. s

157 lagic colonial cnidarians that use tentilla (tentacle side branches armed with nematocysts) exclusive

158 The tentacled snake's facial appendages are superficially si

159 Here, it is reported that tentacled snakes (Erpeton tentaculatus) exploit this nor

160 Tentacled snakes act as rare enemies, taking advantage o

161 Catania provides an introduction to tentacled snakes and their ingenious ability to capture

162 Star-nosed moles and tentacled snakes have exceptional mechanosensory systems

163 and Wnt expression, which delineates arm and tentacle sucker fields.

164 aracteristic lepidopteran proboscis, and the tentacle suggest that the tentacle evolved quickly throu

165 but also as far apically as the base of the tentacles, suggest that this meprin-class metalloprotein

166 e ciliated receptor cells observed along the tentacle surface.

167 ween tentacles, providing the mechanisms for tentacle synchronization.

168 Soft robotic tentacles that move in three dimensions upon pressurizat

169 chids" possess a basal calyx encircled by 18 tentacles that surround the mouth.

170 tain globular surface domains and elongated 'tentacles' that reach into the core of the large subunit

171 the nerve ring, the osphradium, the cephalic tentacles, the buccal tissues, and the foot, whereas NOS

172 the body column just inferior to the base of tentacles, the region of active cell differentiation or

173 Smaller hydrophobic patches on the tentacles themselves likely interact nonspecifically wit

174 the pigmented region of the ocellus, in the tentacle tip by in situ hybridization, and in the embryo

175 An octopus brings food grasped by a tentacle to its mouth by bending the tentacle around a j

176 bic core, suggesting its potential role as a tentacle to search for OST.

177 esting CP uses two independent actin binding tentacles to cap the barbed end.

178 of Actinia, a marine predator that uses its tentacles to ensnare food, for the removal of an array o

179 verse mechanoreceptors from hydroid filiform tentacles to jellyfish statocysts.

180 neutrophils use large filopodia as cellular tentacles to sense local environment but also to detect

181 controls directional food transfer from the tentacles to the mouth.

182 and project their fans, composed of radiolar tentacles, up into the water column for respiration and

183 n the key innovation in the moths of complex tentacles used for pollen collecting and active pollinat

184 formed transcriptome sequencing of dissected tentacles using phylogenetically-informed annotation to

185 The localization of HMP-1 protein in tentacles was confirmed using an enzymatic approach.

186 However, when polyp tentacles were cut into small pieces, the fragments rema

187 en compared with the innervation of cephalic tentacles, which are involved in mechanoreception and po

188 end regeneration, markers for tissue of the tentacles, which lie below the extreme oral end (the hyp

189 r to, and directly above, the zone where the tentacles will emerge, but is not observed nearby when t

190 determined a bound conformation of the beta tentacle with V-1 that is consistent with these findings

191 We propose that comb rows are derived from tentacles with paired sets of pinnules that each bear a

192 Chordata ribosomes present polymorphic tentacles with the potential to switch between inter- an

193 classes of multicellular stalked glands (or tentacles) with an apical pore.

194 g ipsilateral head turning, head withdrawal, tentacle withdrawal, feeding, and locomotion.

195 the gene is expressed in the ectoderm of the tentacle zone and hypostome, but not in the tentacles.

196 enes whose expression is associated with the tentacle zone are ectopically expressed upon exposure to

197 ith body column tissue are turned off as the tentacle zone expands.

198 ing the border between the hypostome and the tentacle zone.

199 homeotic transformation of body column into tentacle zone.