ライフサイエンスコーパス: rhombic

1 easured in a single alignment medium that is rhombic.

2 3-2.07 signal (g = 2.3-2.07, 1.863) and/or a rhombic 2.08 signal (g = 2.077, 1.935, 1.880).

3 Oxidized CrHydA1 displayed a rhombic 2.1 EPR signal (g = 2.100, 2.039, 1.997) and an

4 e orientation of the riboses relative to the rhombic alignment tensor of the molecule studied, a stem

5 The EPR signal is rhombic and consists of two overlapping S = ½ spe

6 entify an unusual EPR signal with very small rhombic anisotropy and g values of 2.02, 1.99, and 1.96.

7 scales, specifically from the terminal umbo, rhombic apophysis, and cuticle structure.

8 Dinuclear gold(III) clusters with a rhombic Au(2)O(2) core and 2,2'-bipyridyl ligands substi

9 controlled by the His-Fe-His vector, and the rhombic axes are controlled by the mean of the imidazole

10 several Raman bands revealed an increase of rhombic B(1g) distortion with respect to native HRP in w

11 ifferent molecular environments, including a rhombic Be2 X2 (X=C, N) core, a vertical Be-Be axis in a

12 ce M3 receptor population is a tetramer with rhombic, but not linear, orientation.

13 ), g-strain and broadening from the possible rhombic character of the Zeeman interaction are small.

14 tical spectrum; (2) its EPR spectrum showing rhombic character to its Type 1 center and nitrite pertu

15 eutral radical, the g-matrix has significant rhombic character, but this is significantly decreased i

16 We observe twinning of two-dimensional (2D) rhombic colloidal crystals of hard Brownian rhombic plat

17 ulation of these spectra yield the axial and rhombic components of the Mn(2+) (S = (5)/(2)) zero-fiel

18 rs between a hexagonal rotator crystal and a rhombic crystal.

19 is key feature, which is not readily seen in rhombic crystals of square colloids, facilitates observa

20 uidistant between two 'anchor' metal ions: a rhombic dipolar interaction tensor, T approximately [T,

21 This correlates with the rhombic distortion caused by the M98Q mutation that is c

22 he coupling of band III to modes with strong rhombic distortion of the heme macrocycle calls into que

23 d M98Q amicyanin, which exhibits significant rhombic distortion of the type 1 site.

24 ar) part of the spectrum is sensitive to the rhombic distortion parameters A(x) and A(y).

25 ll {110}-faceted gold nanostructures, namely rhombic dodecahedra (RD) and triangular bipyramids (BPs)

26 Two imidazolate-metal based rhombic dodecahedra (termed MOP-100 and MOP-101) were de

27 l-regulated crystal orientation not only for rhombic dodecahedra all of whose facets are equivalent,

28 Two {110}-faceted gold nanostructures--rhombic dodecahedra and obtuse triangular bipyramids--ha

29 ra, {100}-truncated rhombic dodecahedra, and rhombic dodecahedra are approximately 200, 140, 270, and

30 the three-dimensional Pt anisotropy of Pt-Ni rhombic dodecahedra can be tuned by controlling the rati

31 The rhombic dodecahedra exposing only the {110} facets exhib

32 Both rhombic dodecahedra show unusual chemical stability in a

33 Rhombic dodecahedra were assembled into truncated triang

34 corner-truncated octahedra, {100}-truncated rhombic dodecahedra, and rhombic dodecahedra are approxi

35 the shapes of spheres, cubes, octahedra and rhombic dodecahedra, we investigate the entire self-asse

36 ary trajectory of phase segregation in Pt-Ni rhombic dodecahedra.

37 d a substantially slower growth rate for the rhombic dodecahedra.

38 olor change takes 10-20 min in the growth of rhombic dodecahedra.

39 iderable variation and form micrometer-sized rhombic dodecahedral cubosome particles.

40 In this study, rhombic dodecahedral gold nanocrystals were used as core

41 l, {100}-truncated rhombic dodecahedral, and rhombic dodecahedral structures have been synthesized.

42 ncated rhombic dodecahedral, {100}-truncated rhombic dodecahedral, and rhombic dodecahedral structure

43 Cubic, rhombic dodecahedral, octahedral, and corner-truncated o

44 Rhombic dodecahedral, octahedral, and hexapod-shaped sup

45 r-truncated octahedral, all-corner-truncated rhombic dodecahedral, {100}-truncated rhombic dodecahedr

46 on of ultrasonic irradiation afforded hollow rhombic-dodecahedral crystals of the C-methylcalix[4]res

47 gh the 14 axes to the 24 edges such that the rhombic dodecahedron becomes a Pt-rich frame enclosing a

48 At the micrometer scale, the anisotropic rhombic dodecahedron crystal habit couples with photonic

49 ubic habit from cube-shaped nanoparticles, a rhombic dodecahedron habit from octahedron-shaped nanopa

50 ies defined by the mesoscale crystal (here a rhombic dodecahedron) by controlling the spacing between

51 esults in Pt segregation to the 14 axes of a rhombic dodecahedron, forming a highly branched, Pt-rich

52 nanoparticles, and an octahedron habit from rhombic dodecahedron-shaped nanoparticles.

53 ink the particles together, in the form of a rhombic dodecahedron.

54 polyhedrons, namely, truncated octahedrons, rhombic dodecahedrons, hexagonal prisms, cubes, gyrobifa

55 pectra for ferrous N694G and an intermediate rhombic electron paramagnetic resonance (EPR) signal for

56 is from a transient species that displays a rhombic electron paramagnetic resonance (EPR) signal wit

57 es a novel Ni(p)(+) species (A(red)*) with a rhombic electron paramagnetic resonance spectrum (g valu

58 x is defined as a ferric high-spin heme in a rhombic environment.

59 The as-purified enzyme exhibited a rhombic EPR signal characteristic of the ready nickel-bo

60 rk, the change from "large g(max)" to normal rhombic EPR signal occurs between axial ligand plane dih

61 ation (under argon) the H cluster exhibits a rhombic EPR signal that is not seen in the as-purified e

62 t of the enzyme results in conversion of the rhombic EPR signal to a g = 6 signal, consistent with fo

63 over many similar sites, the A-center has a rhombic EPR signal with a g-tensor, g(A) = [2.248(4), 2.

64 ed hydrazine-FeMo-cofactor adduct displays a rhombic EPR signal with g = [2.09, 2.01, 1.93].

65 The enzyme as isolated exhibits a rhombic EPR signal with g values of 2.5, 2.3, and 1.86,

66 structures with apical oxo ligands, exhibit rhombic EPR spectra, and 3-5 are electrochemically reduc

67 nd sets in the ferric state and give rise to rhombic EPR spectra.

68 f the double mutants (C52S/C95A) exhibited a rhombic EPR spectrum.

69 It has a rhombic g tensor (2.007, 1.937, 1.897) with an average g

70 -band EPR spectrum of the radical exhibits a rhombic g tensor with dual gx values (2.00550 and 2.0060

71 EPR spectroscopy reveals rhombic g- and A-tensors that indicate a low-symmetry ge

72 The rhombic g-tensor and observed hyperfine coupling to 57Fe

73 the [4Fe-4S](+) of PFL-AE, changing it from rhombic (g = 2.02, 1.94, 1.88) to nearly axial (g = 2.01

74 O(2) to generate an intermediate (H) with a rhombic, g < 2 EPR spectrum; (2) a form of the enzyme wi

75 en well documented, has the highest level of rhombic heme (41-fold greater than for HbA(0)), even tho

76 The rhombic heme measured by electron paramagnetic resonance

77 Thereby, the high spin ferric rhombic heme spectrum became similar to lactoperoxidase,

78 dandelion-like assemblages from Pt NCs, and rhombic/hexagonal platelet assemblages from PdS NCs and

79 e with two or three cysteinate ligands and a rhombic high spin (S = 2) Fe(II) center (E/D = 0.28, D =

80 active site iron center in oxidized SOR from rhombic high-spin ferric (S = 5/2) to axial-like low-spi

81 The results reveal a rhombic intermediate-spin (S = 3/2) Fe(III) center (E/D

82 weak signal at g = 4.3, which we ascribe to rhombic iron and a free radical signal at g(ave) = 2.01.

83 The rhombic lattice angle alpha increases continuously with

84 kwise, from the average pointing axis of the rhombic lattice yielding a form of nonlocal chiral symme

85 which have higher symmetry but can also form rhombic lattices at high densities, each rhombic particl

86 s are more frequently expressed in the lower rhombic lip (LRL) and embryonic dorsal brainstem than in

87 The lower rhombic lip (LRL) is a germinal zone in the dorsal hindb

88 ield that adjoins a germinal zone, the lower rhombic lip (LRL), functions as a progenitor domain by c

89 ins within and outside the hindbrain (lower) rhombic lip (LRL).

90 imordium contains two germinative zones, the rhombic lip (RL) and the ventricular zone (VZ), which ge

91 The rhombic lip (RL) is an embryonic proliferative neuroepit

92 The rhombic lip (RL) is the neuroepithelium immediately adja

93 equirement of Pax6 in the development of all rhombic lip (RL) lineages.

94 ral progenitors originating from the rostral rhombic lip (RRL).

95 embryonic dorsal brainstem than in the upper rhombic lip (URL) and developing cerebellum.

96 The upper rhombic lip (URL), a germinal zone in the dorsoanterior

97 Expression of atonal1 in the rhombic lip adjacent at the roof plate boundary is acute

98 eal molecular organization of the cerebellar rhombic lip and introduce Lmx1a as an important regulato

99 Math1 expression delimits the extent of the rhombic lip and is required for the generation of the hi

100 for specification of the adjacent cerebellar rhombic lip and its derivative fates.

101 cification of cerebellar cell types from the rhombic lip and its upregulation inhibits their producti

102 indbrain, arise from precursors in the lower rhombic lip and migrate anteroventrally to reach their f

103 that DCN neurons in mice are produced in the rhombic lip and migrate rostrally in a subpial stream to

104 Our results suggest that UBCs arise from the rhombic lip and migrate via novel pathways to their fina

105 h are critical for maintenance of the entire rhombic lip and normal cerebellar morphogenesis.

106 of Lmx1a, these cells precociously exit the rhombic lip and overmigrate into the anterior vermis.

107 1 is the defining molecule of the cerebellar rhombic lip and Pax6 is downstream in the Math1 pathway.

108 associated with premature regression of the rhombic lip and posterior vermis hypoplasia in Lmx1a(-/-

109 hl1 homeobox gene is highly expressed by the rhombic lip and rhombic lip-derived migratory neurons.

110 The cerebellar rhombic lip and telencephalic cortical hem are dorsally

111 ere derived from neuronal progenitors of the rhombic lip and that cerebellar ectopia were derived fro

112 jor precerebellar nuclei that arise from the rhombic lip and that issue mossy fibers.

113 arate progenitor pools located mainly in the rhombic lip and the cerebellar ventricular zone, respect

114 existence of spatial compartmentation in the rhombic lip and the interplay between Wls, Math1, and Pa

115 However, the cerebellum's upper rhombic lip and the optic tectum are abnormal in clo.

116 f cells originating from both the cerebellar rhombic lip and the telencephalic cortical hem.

117 The rhombic lip and ventral midline express Slit2 and both e

118 Thus, proliferating precursors within the rhombic lip are specified to be granule cells very early

119 the earliest granule cell progenitors at the rhombic lip as they separate from the ventricular zone o

120 g granule cell progenitors isolated from the rhombic lip at E14 or from the external germinal layer a

121 nce for an hCPe contribution directly by the rhombic lip at late embryonic stages when hRPe is no lon

122 ansformed our understanding of the embryonic rhombic lip by revealing the inductive cues, regional or

123 We also examine five rhombic lip cell markers (Wls, Math1, Pax6, Lmx1a, and T

124 introduce Lmx1a as an important regulator of rhombic lip cell-fate decisions, which are critical for

125 ggests that Sef may normally function in non-rhombic lip cells and prevent them from responding to FG

126 In the mouse embryo, rhombic lip cells express a number of granule neuron mar

127 When transplanted into younger neural tube, rhombic lip cells maintain their characteristic molecula

128 Isolation of rhombic lip cells reveals a homogenous population of pre

129 Cerebellar rhombic lip derivatives demonstrate a temporal organisat

130 n hindbrain specification and generate upper rhombic lip derivatives on exposure to bone morphogeneti

131 trin orchestrates the migration of hindbrain rhombic lip derivatives to form the precerebellar nuclei

132 gregate the roof plate lineage from neuronal rhombic lip derivatives.

133 l precursor cells generated within the upper rhombic lip directly.

134 more than one cell type, indicating that the rhombic lip does not consist of a homogeneous population

135 ull mice have embryonic abnormalities of the rhombic lip due to loss of mesenchyme-secreted signaling

136 our molecularly distinct compartments in the rhombic lip during cerebellar development.

137 ulture experiments, Tbr2+ UBCs migrated from rhombic lip explants directly into the developing white

138 Dorsal midline cells adjacent to the rhombic lip express Bmp6, Bmp7 and Gdf7, three genes enc

139 d in grafted progenitors: transplanted early rhombic lip fails to subsequently produce granule cell p

140 We find that the anterior rhombic lip gives rise to more than one cell type, indic

141 Thus, we demonstrate that the cerebellar rhombic lip gives rise to multiple cell types within rho

142 The rhombic lip gives rise to neuronal populations that cont

143 Ablation of the rhombic lip in organotypic slice cultures substantially

144 ence of Wls-positive cells in the Math1-null rhombic lip indicates that Wls expression is independent

145 The rhombic lip is a discrete strip of neuroepithelium borde

146 These findings suggest that the rhombic lip is dynamically patterned by the expression o

147 eed, the production interval for hCPe by the rhombic lip is surprisingly extensive.

148 The rhombic lip is thus emerging as a spatiotemporally disti

149 from the Math1 locus, a molecular marker of rhombic lip lineages.

150 ve cells and their progeny that arise in the rhombic lip of the cerebellar primordium during embryoge

151 zone precursors and glutamatergic cell from rhombic lip precursors, mirroring distinct origins for t

152 ental progression has been assumed, with the rhombic lip producing non-mitotic hRPe, and seemingly un

153 e neural tube, derivatives of early and late rhombic lip progenitors display patterns of migration an

154 Modelling of mutations in mouse lower rhombic lip progenitors that generate WNT-subgroup tumou

155 addition, Lmx1a is expressed in a subset of rhombic lip progenitors which produce granule cells that

156 in restricting vz progenitors from becoming rhombic lip progenitors.

157 nterplay between Wls, Math1, and Pax6 in the rhombic lip provides novel views of early cerebellar dev

158 dbrain dorsal interneurons that comprise the rhombic lip relay sensory information and coordinate mot

159 ker of the cells in the interior face of the rhombic lip throughout normal mouse cerebellar developme

160 postnatally, after their migration from the rhombic lip to the external germinal layer.

161 granule cell precursors are generated at the rhombic lip together with neurons of the lateral pontine

162 The neurons generated at the germinal rhombic lip undergo long distance migration along diverg

163 red gene interactions during the presence of Rhombic lip versus the presence of distinct internal gra

164 2+ UBCs appeared to migrate out of the upper rhombic lip via two cellular streams: a dorsal pathway i

165 In organotypic slice cultures, the rhombic lip was necessary and sufficient to produce cell

166 blishment of a neural progenitor population (rhombic lip) that gives rise to multiple hindbrain struc

167 ated protein kinase pathway is active in the rhombic lip, a germinal zone that generates diverse type

168 iferative state, order of emergence from the rhombic lip, and molecular profile of either the constit

169 mutant mice, Tbr2+ UBCs accumulated near the rhombic lip, consistent with impaired migration through

170 The rhombic lip, from which granule cell precursors arise, a

171 d along the dorsal-most region of the caudal rhombic lip, gives rise to the cochlear and precerebella

172 Sef is expressed immediately adjacent to the rhombic lip, overlapping with FGF15 and FGFR1, which is

173 valent to the medial ganglionic eminence and rhombic lip, resembling the gnathostome brain.

174 rsors of cerebellar granule neurons from the rhombic lip, the dorsal aspect of the midbrain/hindbrain

175 erivatives is intrinsically specified at the rhombic lip, the orderly temporal transition in cell typ

176 which gives rise to isthmic nuclei, and the rhombic lip, which generates deep cerebellar nuclei and

177 enitor zones, the ventricular zone and upper rhombic lip, which give rise to distinct cell types in t

178 n orientated, active migration away from the rhombic lip, which is apparently independent of either g

179 A subset of rhombic lip-derived cells also express reelin, a key reg

180 The rhombic lip-derived cells express transcription factors

181 which have a severe cerebellar malformation, rhombic lip-derived cells migrated to the NTZ, despite r

182 nd positioning of fissures, whereas in upper rhombic lip-derived cells the genes are more important i

183 mic FGF signals is required for induction of rhombic lip-derived cerebellar neurons.

184 -lateral coordinates into the adult, whereas rhombic lip-derived granule cells undergo lateral to med

185 ineage appears to be unique among the varied rhombic lip-derived lineages in its proliferative respon

186 e is highly expressed by the rhombic lip and rhombic lip-derived migratory neurons.

187 ctive deficit occurs without affecting other rhombic lip-derived nuclei, despite expression of Math1

188 poptosis, indicating that VZ/SVZ-derived and rhombic lip-derived progenitor cells show differential r

189 ral auditory system neurons derived from the rhombic lip.

190 of granule precursor cells derived from the rhombic lip.

191 rsal neuroectodermal progenitor cells of the rhombic lip.

192 expression of Math1 and Tcf4 throughout the rhombic lip.

193 n trajectories, i.e. the floor plate and the rhombic lip.

194 have a predetermined spatial address in the rhombic lip.

195 onset of their genesis in the mouse anterior rhombic lip.

196 igate tangential neuronal migration from the rhombic lip.

197 of the mesencephalon and metencephalon, the rhombic lip.

198 lockade reduces the length of the cerebellar rhombic lip.

199 ch are localized to the exterior face of the rhombic lip.

200 cerebellar nuclei that arise from the caudal rhombic lip.

201 een the non-neural roof plate and the neural rhombic lip.

202 euroepithelia: the ventricular zone (VZ) and rhombic lip.

203 We uncover a Math1-dependent rostral rhombic-lip migratory stream (RLS) that generates some n

204 selective knock-out of P/Q-type channels in rhombic-lip-derived neurons including the PF and MF path

205 use many precerebellar nuclei originate from rhombic lips, the first analysis of neuronal migrations

206 esponsible for the strong positive axial and rhombic magnetic anisotropy of the high-spin Co(II) ion

207 The rhombic magnetic axes in S92A-metMbCN are rotated approx

208 edicted by the change in the location of the rhombic magnetic axes.

209 rate FeMo cofactor, is a S=3/2 system with a rhombic magnetic g tensor.

210 similar to a fly's eye); and (iv) arrays of rhombic microlenses.

211 ignificantly contributes to constructing the rhombic nanoporous network, whereas carboxylic acid amph

212 ainstem system derives from dorsally located rhombic neuroepithelium.

213 'order-by-disorder' effect that favours the rhombic over other zigzagging configurations.

214 orm rhombic lattices at high densities, each rhombic particle has a distinguishable bidirectional poi

215 ioheme I, and the known essentially constant rhombic perturbation of heme pocket sites on the hyperfi

216 han that of the axial His, that modulate the rhombic perturbation to the heme's in-plane electronic a

217 -order transition between the square and the rhombic phase and different regimes of elasticity, as we

218 rhombic colloidal crystals of hard Brownian rhombic platelets.

219 ncated icosahedron or soccer ball--and the 2 rhombic polyhedra reported by Johannes Kepler in 1611.

220 Like the faces in Kepler's rhombic polyhedra, the 6gon faces in Goldberg polyhedra

221 c site symmetry determining whether axial or rhombic resonance patterns are observed.

222 Fe-NO adduct of FeSOD (NO-FeSOD) exhibit two rhombic S = 3/2 signals of comparable population; E/D =

223 The results reveal a rhombic S = 5/2 linear [Fe3S4](+) cluster with propertie

224 se from the middle Kramers doublet of a near rhombic S = 5/2 system.

225 f FeMo cofactor was observed to convert to a rhombic, S = 1/2, signal (g = [2.08, 1.99, 1.97]).

226 ituted ImiS demonstrated the appearance of a rhombic signal after 10 ms that is assigned to a reactio

227 For the paral-[FeOMTPP(1-MeIm)(2)]Cl, a rhombic signal with g(1) = 1.54, g(2) = 2.51, and g(3) =

228 ](+) exhibits both "large g(max)" and normal rhombic signals, suggesting the presence of both "perpen

229 present different shapes, such as hexagonal, rhombic, six-cornered star, dumbbell, or dendritic.

230 The spectrum displays rhombic symmetry and is indicative of a high-spin heme.

231 of the component spins of the triplets have rhombic symmetry because of electron spin delocalization

232 th axial symmetry and one low-spin heme with rhombic symmetry.

233 n I-II-helix VIII dimers interact to form a "rhombic" tetramer via an interface involving residues fr

234 surface occupy the positions of atoms in the rhombic triacontahedral cluster, the building block of t

235 square particle shape combine to produce the rhombic unit cell.

236 2D nanoporous molecular networks containing rhombic voids are demonstrated to be accessible from low

237 allel = 98 x 10(-4) cm(-1), and another more rhombic, with a smaller A parallel value of 69 x 10(-4)

238 /- 2 cm(-1) (where D and E are the axial and rhombic zero-field splitting parameters, respectively) a

239 uclear center of Mn/Mn-PTE requires slightly rhombic zero-field splitting parameters.

240 The fast QTM rate suggested a significant rhombic ZFS parameter E, as expected from the low (virtu