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 The latter is split by weak axial and rhombic anisotropies.

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

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

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

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

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

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

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

14 ental observations, it is proposed here that rhombic calcite microcrystals form exclusively in meteor

15 Furthermore, the hypothesis that rhombic calcite microcrystals form exclusively in meteor

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

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

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

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

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

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

22 Holococcoliths consisting of simple rhombic crystals can be produced by the haploid life cyc

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

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

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

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

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

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

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

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

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

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

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

34 overcomes this failure mode by leveraging Li rhombic dodecahedra as nucleation seeds, enabling the su

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

36 In a coin cell architecture, these rhombic dodecahedra exhibit near point-contact connectiv

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

38 Both rhombic dodecahedra show unusual chemical stability in a

39 Rhombic dodecahedra were assembled into truncated triang

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

41 ion of crystal symmetry in cubes, octahedra, rhombic dodecahedra, and their truncated variants.

42 e for a particular crystal morphology (e.g., rhombic dodecahedra, stacked clusters, and smooth rods).

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

44 ic NPs of three shapes-cubes, octahedra, and rhombic dodecahedra-on substrates and investigate their

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

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

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

48 mechanical vibrations to assemble 3D printed rhombic dodecahedral and truncated octahedral grains int

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

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

51 s on the three-dimensional toric code on the rhombic dodecahedral lattice with boundaries and prove t

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

53 oordinated 12-c cuboctahedral cluster from a rhombic dodecahedral ZIF-8 particle.

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

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

56 Rhombic dodecahedral, octahedral, and hexapod-shaped sup

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

58 The shape remained rhombic dodecahedral-tetrahedral, and the phase retained

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

60 ron microscopy (TEM), we show that cubic and rhombic dodecahedron (RD) ZIF-8 NPs convert into hollow

61 plasmonic Au nanoparticles - nanocube (NC), rhombic dodecahedron (RD), and octahedron (OC) - exposin

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

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

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

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

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

67 on morphology of metallic Li to be that of a rhombic dodecahedron, which is surprisingly independent

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

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

70 thesize an unreported shape, which is the Cu rhombic dodecahedron.

71 um spin-space described by the vertices of a rhombic dodecahedron.

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

73 ({200}, {020}, {112}) and led to 12 faceted rhombic dodecahedrons.

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

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

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

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

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

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

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

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

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

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

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

85 , these molecules are highly anisotropic and rhombic EPR spectra for the Ce(III) complex are reported

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

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

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

89 uration, high fluid:solid ratio) exhibit the rhombic form/morphology, whereas calcite microcrystals c

90 ndicative of meteoric diagenesis whereas non-rhombic forms are associated with marine burial conditio

91 turation, low fluid:solid ratio) exhibit non-rhombic forms.

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

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

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

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

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

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

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

99 The rhombic heme measured by electron paramagnetic resonance

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

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

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

103 Heme alphaI exhibited a rhombic high spin signal, in line with its ligation by a

104 high-spin (S = 1) ground state and displays rhombic high-frequency and -field electron paramagnetic

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

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

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

108 The rhombic lattice angle alpha increases continuously with

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

110 diameter and ~250 nm height, that provides a rhombic-lattice canvas of a thousand pixels each, with p

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

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

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

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

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

116 tly localizes to the ventricular zone of the rhombic lip (RL(VZ)).

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

118 lling lead to Sonic hedgehog MB in the upper rhombic lip (RL) granule cell lineage(5-8).

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

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

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

122 fferentiation, hbNES cells transit through a rhombic lip (RL) progenitor state at day 7, demonstratin

123 tely anterior to the morphologically defined rhombic lip (RL).

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

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

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

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

128 regulator in both the normal and transformed rhombic lip and identifying ZIC1 as an exquisitely conte

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

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

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

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

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

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

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

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

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

138 1 is the defining molecule of the cerebellar rhombic lip and Pax6 is downstream in the Math1 pathway.

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

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

141 The cerebellar rhombic lip and telencephalic cortical hem are dorsally

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

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

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

145 interface between columnar epithelium of the rhombic lip and the expanding squamous epithelium of the

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

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

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

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

150 ory progenitor populations-specifically, the rhombic lip and ventricular zone progenitors, respective

151 While CN neurons derived from the rhombic lip are positioned in the caudodorsal area of th

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

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

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

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

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

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

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

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

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

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

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

163 Cerebellar rhombic lip derivatives demonstrate a temporal organisat

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

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

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

167 Disruptions in human rhombic lip development are associated with posterior ce

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

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

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

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

172 ess p75NTR when they migrate either from the rhombic lip during embryonic development or from the EGL

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

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

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

176 ing human tissues(3)-particularly within the rhombic lip germinal zone, which produces all glutamater

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

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

179 The rhombic lip gives rise to neuronal populations that cont

180 Distinct ZIC1 mutations affect cells of the rhombic lip in diametrically opposed ways, suggesting th

181 Ablation of the rhombic lip in organotypic slice cultures substantially

182 subgroups to their unified beginnings in the rhombic lip in the early stages of human development.

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

184 The rhombic lip is a discrete strip of neuroepithelium borde

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

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

187 The rhombic lip is thus emerging as a spatiotemporally disti

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

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

190 of CN neurons that do not originate from the rhombic lip or ventricular zone of the cerebellar primor

191 program that is mirrored in human cerebellar rhombic lip origins.

192 The human rhombic lip persists longer through cerebellar developme

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

194 iotemporal expansion of both ventricular and rhombic lip primary progenitor zones to include subventr

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

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

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

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

199 in restricting vz progenitors from becoming rhombic lip progenitors.

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

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

202 Oncogenic transformation of early Prtg(+ve) rhombic lip stem cells initiates group 3 medulloblastoma

203 s, PPHLN1 is expressed in the most primitive rhombic lip stem cells, and targeting PPHLN1 splicing re

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

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

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

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

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

209 2+ UBCs appeared to migrate out of the upper rhombic lip via two cellular streams: a dorsal pathway i

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

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

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

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

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

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

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

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

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

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

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

221 ns arising from the ventricular zone and the rhombic lip, two distinct germinal zones of the embryoni

222 generated from a unique progenitor zone, the rhombic lip, whereas the inhibitory neurons and astrocyt

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

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

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

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

227 The rhombic lip-derived cells express transcription factors

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

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

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

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

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

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

234 et shows that WNT medulloblastomas match the rhombic lip-derived mossy fiber neuronal lineage and emb

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

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

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

238 ral auditory system neurons derived from the rhombic lip.

239 rsal neuroectodermal progenitor cells of the rhombic lip.

240 expression of Math1 and Tcf4 throughout the rhombic lip.

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

242 have a predetermined spatial address in the rhombic lip.

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

244 igate tangential neuronal migration from the rhombic lip.

245 of granule precursor cells derived from the rhombic lip.

246 of the mesencephalon and metencephalon, the rhombic lip.

247 lockade reduces the length of the cerebellar rhombic lip.

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

249 cerebellar nuclei that arise from the caudal rhombic lip.

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

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

252 Molecular signatures encoded within a human rhombic-lip-derived lineage trajectory aligned with phot

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

254 s normally arise only in the lower and upper rhombic lips, respectively.

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

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

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

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

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

260 y of Phanerozoic limestones characterized by rhombic microcrystals also exhibit petrographic and/or g

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

262 ed of hybrid plasmonic waveguide (HPW)-based rhombic nano-antenna, polarization beam splitter, couple

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

264 ainstem system derives from dorsally located rhombic neuroepithelium.

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

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

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

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

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

270 rhombic colloidal crystals of hard Brownian rhombic platelets.

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

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

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

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

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

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

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

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

279 ned, which coincided with an increase in the rhombic signal intensity.

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

281 hree distinct EPR signals: S = 1/2 axial and rhombic signals, and a high-spin S = 7/2 signal.

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

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

284 The rhombic superlattice assembled from SD/Ag78a through int

285 The rhombic superlattice assembled from SD/Ag78a through int

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

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

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

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

290 In addition, a possible rhombic-to-square vortex lattice phase transition is als

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

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

293 2D nanoporous molecular networks containing rhombic voids are demonstrated to be accessible from low

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

295 /- 2 cm(-1) (where D and E are the axial and rhombic zero-field splitting parameters, respectively) a

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

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