ライフサイエンスコーパス: torus

1 mutating the outer surface of the betagamma torus.

2 gravitational potential and the surrounding torus.

3 , brighter on the pole closest to the plasma torus.

4 e circumferentially wound DNA strands in the torus.

5 id bends back on itself like the inside of a torus.

6 bility by merging with an unstable invariant torus.

7 onds to currents flowing on the surface of a torus.

8 ures in the inner nebula including a jet and torus.

9 re significant for mechanical support of the torus.

10 leading to images of an embedding of a flat torus.

11 of the pore with respect to the edge of the torus.

12 s interaction with the Enceladus neutral gas torus.

13 nward on the new cross-wall and thus forms a torus.

14 apoA-I to a plane inside of an alpha-helical torus.

15 ically self-confined current-carrying plasma torus.

16 All three nuclei of the torus also have reciprocal connections with the superior

17 rior semicircular canal, absence of a nuchal torus and a suprainiac fossa, and a small occipital bun.

18 oepithelial locations into BT units near the torus and BM units at intermediate sites.

19 the binary is comparable to the size of the torus and broad-line region, the feeding of the black ho

20 The torus and ionosphere are also depleted by three time-var

21 fraction of resistance to flow, whereas the torus and margo pores formed a large fraction, which dep

22 th-long monitoring campaign of the Io plasma torus and neutral cloud was conducted to determine the c

23 They share occipital (suprainiac and nuchal torus) and temporal labyrinthine (semicircular canal) mo

24 ea, hypothalamus, optic tectum, semicircular torus, and caudal midbrain tegmentum, but conspicuous pr

25 ole in a binary system is believed to form a torus around a Kerr black hole.

26 four-stranded beta-sheets are arranged in a torus around a pseudosymmetric axis.

27 even four-stranded beta-sheets arranged in a torus around a pseudosymmetry axis.

28 at GFP-tagged HsSAS-6 variants localize in a torus around the base of the parental centriole before S

29 Mutation of residues along the side of the torus at blade 1 diminish affinity for alpha but do not

30 strong magnetic field to form a co-rotating torus at Io's distance; the remaining ions and electrons

31 atenin/Tcf and Blimp1, repression within the torus by Hox11/13b, and repression outside the torus by

32 rus by Hox11/13b, and repression outside the torus by Tcf in the absence of Wnt8 signal input.

33 es located on separate rings of right-handed torus catenanes containing six or more nodes.

34 thermore, parallel psi sites on right-handed torus catenanes were not substrates for Xer recombinatio

35 ent molecules deduced from the volume of the torus compares well with those obtained on the same samp

36 cterized by a pseudo symmetric heterodimeric torus containing a small channel that is positively char

37 eids decreases steadily with height, whereas torus diameter remains relatively constant.

38 e structure transformation from spherical to torus, disk-shaped geometries and tubular assemblies.

39 such models cannot explain or predict failed torus events.

40 We find that such 'failed torus' events occur when the guide magnetic field (that

41 eld inside the droplets and show that as the torus evolves, its cross-section significantly deviates

42 h an optical trap to examine the kinetics of torus formation induced by the binding of protamine and

43 Torus fractures predominated, and these patterns were co

44 the cis-regulatory level by the blimp1-wnt8 torus-generating subcircuit now explains the progression

45 blimp1 and wnt8, are members of a cohort of torus genes with similar regulatory inputs and similar,

46 modes of penetration are observed in the CD torus; however, there is a 0.985-A shift in the position

47 These amino acids on the beta-torus identify a region that is distinct from those regi

48 nding efferents from all three nuclei of the torus innervate central and lateral thalamic nuclei, and

49 gnetohydrodynamic force imbalance called the torus instability.

50 in the magnetic topology, as in the kink or torus instability; and coronal jets from a resistive pro

51 t ejects sodium only from the wake of the Io-torus interaction, together with a visually distinct, sp

52 he experimentally obtained velocities at the torus interface to theoretically reconstruct the interna

53 The outer surface of the betagamma torus is largely made from outer beta strands of the pro

54 ional energy of a black hole surrounded by a torus is released through several channels.

55 chiral knot 4(1) and the predominance of the torus knot 5(1) over the twist knot 5(2) observed in the

56 ost common substrates: unknots, unlinks, and torus knots and catenanes.

57 norientable surfaces and use it to construct torus knots and links of type (p,2) around multiply twis

58 nteractions between particle-like skyrmionic torus knots of molecular alignment field, which can be t

59 We also find that the family of (2, 2k+1) torus knots unravel gradually by simplifying their topol

60 he knots found belong to the small family of torus knots.

61 trefoil or pentafoil, or even of more exotic torus knots.

62 ucleus and the lateral hypothalamus (lateral torus, lateral recess nucleus, hypothalamic inferior lob

63 the dorsomedial nucleus of the thalamus, the torus lateralis of the ventral hypothalamus, and the pre

64 ferior lobe, and the nucleus diffuses of the torus lateralis.

65 Their torus-like spatial expression patterns and gene regulato

66 a nonlinear increase in loss from the plasma torus, limiting plasma buildup.

67 lar results were obtained in recordings from torus longitudinalis.

68 rane and a typical gymnosperm conduit with a torus-margo pit membrane structure.

69 basis than vessel pits, owing to the unique torus-margo structure of the conifer pit membrane.

70 For conduits with torus-margo type pits pit membrane deflection was also m

71 k mechanism in which increases in the plasma torus mass cause a nonlinear increase in loss from the p

72 ent increase in the neutral cloud and plasma torus masses.

73 sed osteogenic differentiation of mandibular torus MSCs was associated with the suppression of Notch3

74 Mandibular torus (MT) is a common intraoral osseous outgrowth locat

75 ier that this circuit generates an expanding torus of blimp1 and wnt8 expression.

76 he upper atmosphere of Jupiter itself, and a torus of emission residing just outside the orbit of Jup

77 wnt8, and blimp1 genes accounts for a moving torus of gene expression that sweeps concentrically acro

78 in the sea urchin embryo depends on a moving torus of regulatory gene expression.

79 he packing of the guest molecules inside the torus of the CD changes upon substitution of a methoxy g

80 lecule is included deeply in the hydrophobic torus of the extended dimer host.

81 Relative to terrestrial anurans, the torus of X. laevis is hypertrophied and occupies the ent

82 Each xenon(II) atom is surrounded by a torus of xenon valence electron density comprised of the

83 es 'trapped' on the mica as partially formed toruses of nucleoprotamine.

84 servations reveal an isolated third ring, or torus, of high-energy (>2 MeV) electrons that formed on

85 capsulating polymerized actin assumed mostly torus or disk shapes along with some high aspect ratio t

86 ent with minocycline-induced staining of the torus palatinus and alveolar bone.

87 bone density, with a thickened mandible and torus palatinus, by impairing the action of a normal ant

88 bone density, a wide and deep mandible, and torus palatinus.

89 w resistance was low relative to that of the torus, pore location near the inner edge of the margo al

90 he carbohydrate residues to the cyclodextrin torus, proceeds in moderate-good yields (42-70%) by the

91 entral thalamus, and all three nuclei of the torus receive descending input from the anterior entoped

92 runcation studies show that formation of the torus requires a repeated domain separate from AIR9's mi

93 cycle and a quasiperiodic solution on a two-torus, respectively.

94 nses of one class of auditory neurons in the torus semicircularis (auditory midbrain) of frogs reflec

95 nalyzed the decline in IEG expression in the torus semicircularis (homolog of the inferior colliculus

96 hat this merging takes place in the midbrain torus semicircularis (TS).

97 n deep layers of the dorsal (electrosensory) torus semicircularis (TSd).

98 cluding the nucleus praeeminentialis, dorsal torus semicircularis and optic tectum showed expression

99 ere found only in the laminar nucleus of the torus semicircularis and the anterodorsal tegmental nucl

100 aterally to two nuclei in the tegmentum, the torus semicircularis and the lateral mesencephalic nucle

101 sing analyses that assess the ability of the torus semicircularis as a whole to discriminate among ac

102 pped the connections of the subnuclei of the torus semicircularis in Xenopus laevis to determine whic

103 ed in separate pathways that converge in the torus semicircularis on combination-sensitive neurons, m

104 itory sites in nucleus centralis (NC) in the torus semicircularis show a medial column of retrogradel

105 differential phase-sensitive neurons to the torus semicircularis suggests integration of the two sen

106 ral (DC) telencephalon project to the dorsal torus semicircularis to regulate processing of electroco

107 auditory thalamus and/or auditory midbrain (torus semicircularis).

108 structures (optic tectum, dorsal and ventral torus semicircularis); and (4) basal forebrain, preoptic

109 behavior, including the basal forebrain, the torus semicircularis, and the hypoglossal nuclei (nXII).

110 leus of the preoptic area, septum, striatum, torus semicircularis, and ventromedial nucleus of the hy

111 tivity was seen in the optic tectum, rostral torus semicircularis, central pretectal area, and granul

112 vous system nuclei in the dorsal midbrain or torus semicircularis, homologous to the inferior collicu

113 Present study includes spinal projections to torus semicircularis, hypothalamus, thalamus and the tel

114 lamus and pretectum, in the optic tectum and torus semicircularis, in the mesencephalic tegmentum, in

115 rminate heavily in a lateral division of the torus semicircularis, in the ventral optic tectum, and i

116 rom duration-selective neurons in the anuran torus semicircularis, in vivo.

117 ng of particular interest: the optic tectum, torus semicircularis, isthmus, dorsal and medial nuclei

118 rethalamic and thalamic areas, optic tectum, torus semicircularis, mesencephalic tegmentum, interpedu

119 e brainstem areas included the optic tectum, torus semicircularis, nucleus lateralis valvula, a periv

120 different neurons, whereas in other nuclei (torus semicircularis, octavolateralis area, parvocellula

121 os differed in the three subdivisions of the torus semicircularis, suggesting that, as in birds, the

122 Several ascending fibers extended into the torus semicircularis, thalamic and pretectal areas and i

123 zif268, NGFI-A, and krox-24) throughout the torus semicircularis, the auditory midbrain homolog of t

124 cur in the medial octavolateral nucleus, the torus semicircularis, the medial hindbrain, and the thal

125 aminar, midline, and principal nuclei of the torus semicircularis, whereas the ventral region did not

126 and the ventroposterior nucleus (VP) in the torus semicircularis.

127 hypothalamus, and a group of cells near the torus semicircularis.

128 ly to the lateral posterior subdivision, the torus semicircularis.

129 nuclei: the nucleus praeeminentialis and the torus semicircularis.

130 sal and lateral anterior subdivisions of the torus semicircularis.

131 he lateral lemniscus and some neurons in the torus semicircularis.

132 divisions within the central nucleus of the torus semicircularis.

133 put from the pallium (cortex in mammals) and torus semicircularis.

134 ach other and simultaneously changing into a torus-shape.

135 This torus-shaped area of LvBrac expression remains constant

136 A vortex ring is a torus-shaped fluidic vortex.

137 binds to each of the two outer faces of the torus-shaped GTP cyclohydrolase I.

138 ariety of morphologies, including annular or torus-shaped species, were observed.

139 enesis, the channel becomes organized into a torus-shaped structure ("the nimbus") enriched in protei

140 flgI transposon mutants lacked a torus-shaped structure attached to the flagellar rod, es

141 aves, initially excited by turbulence in the torus, should inflate into a bubble in a time as short a

142 Composition measurements through the torus showed that the spatial distributions of protons,

143 ain moves in a hinge-like manner, sampling a torus space around the proximal end of the iSH2 domain.

144 he type {Mo(57)M'(6)} (M' = Fe(III), V(IV)) (torus structure), {M(72)M'(30)} (M = Mo, M' = V(IV), Cr(

145 eatures, including absence of a supraorbital torus, subrectangular orbits, prominent canine fossae, n

146 redicted division site do not elicit an AIR9 torus, suggesting that AIR9 recognizes a component of th

147 eal a surface patch facing the inside of the torus that is highly evolutionarily conserved and specif

148 n to identify the regions on the side of the torus that might be important for effector interactions.

149 Auditory input to the torus, that arising directly from the dorsal medullary n

150 The torus thickness determined from the curve-fitting protoc

151 nce for extensive mass loading of the plasma torus through the ionization of SO2.

152 rating the capability of the giant inorganic torus to develop relevant supramolecular chemistry, prob

153 The resulting increase in the ratio of torus to pit aperture diameter allows the pits to withst

154 most closely correlated to the ratio of the torus to pit aperture diameter but did not vary systemat

155 The response of the plasma torus to this outburst shows that the interaction betwee

156 d structure of the pits in the case of margo-torus type pit membrane.

157 ously unknown eruption criterion below which torus-unstable flux ropes fail to erupt.

158 ed, however, by observations indicating that torus-unstable flux ropes sometimes fail to erupt.

159 xtinction of expression in the center of the torus, whereas its outward expansion follows reception o

160 ss through the membrane, and the impermeable torus, which functions to isolate gas-filled tracheids.

161 position of the guest molecules in the host torus, which takes place without changing the hydrophobi

162 The remaining fraction is released in torus winds, thermal emissions, and (conceivably) megael

163 s released in gravitational radiation by the torus with angular velocity eta similar 0.2 to 0.5 relat