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 is particularly high in the endoderm of the tentacles.

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

8 sis correlate with shaping of the elongating tentacles.

9 with the sole alpha-helices representing the tentacles.

10 ar, although disproportionately broad, lacks tentacles.

11 uniform distribution of a variable number of tentacles.

12 y affects the epithelial cells that form the tentacles.

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

14 e sensory cells in the ectoderm covering its tentacles.

15 of putative nitrergic sensory neurons in its tentacles.

16 4,000/mm2), and TSCs in the tips of cephalic tentacles (100/mm2).

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

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

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

20 5-HT-IR was observed in neuropil of tentacle and rhinophore ganglia with many transverse 5-H

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 ead regeneration and transdifferentiation of tentacle battery cells.

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

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

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

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

43 and is transcriptionally patterned into four tentacle buds.

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

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

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

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

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

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

50 The alpha tentacle contributes more to capping affinity and kineti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

115 The tentacled snake's facial appendages are superficially si

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

117 Tentacled snakes act as rare enemies, taking advantage o

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

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

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

121 Soft robotic tentacles that move in three dimensions upon pressurizat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

143 homeotic transformation of body column into tentacle zone.