ライフサイエンスコーパス: stripe

1 The correct version states 'Disorder stripes'.

2 e white dashed lines incorrectly read 'Order stripes'.

3 he CCCTC-binding factor (CTCF) anchor of the stripe.

4 metastable overoxidized glass in the purple stripe.

5 Tim Caro introduces why zebras are striped.

6 relations associated with half-filled charge stripes.

7 gradient orthogonal to the ocular dominance stripes.

8 magnetically ordered domains in the form of stripes.

9 rmation in L2/3 blobs and, possibly, some V2 stripes.

10 oping in terms of the physics of fluctuating stripes.

11 anophores from coalescing into adult pigment stripes.

12 their spins organize into patterns known as stripes.

13 dominated spiny stellates compared with thin stripes.

14 are mainly responsible for Verticillium stem striping.

15 reported previously, that the D. erecta eve stripe 2 enhancer (eveS2) fails to drive appreciable exp

16 Using stripe 2 of the even-skipped gene in Drosophila embryos

17 s drives normal eve expression, including in stripe 2.

18 ions of contact, the so-called architectural stripes(3).

19 conservation of clock-like regulation of PR stripe addition in sequentially segmenting species while

20 h distinct magnetic properties, organized as stripes along the MnAs [0001] direction.

21 Interestingly, different canting spin stripes along three 120 degree propagation directions ma

22 confirm that Of-E75A is expressed in PR-like stripes, although it is not expressed in this way in Dro

23 siologically responsive, organelles arise in stripe and interstripe by in-situ differentiation.

24 rystal-arrays architectures, indicating that stripe and interstripe iridophores are different cell ty

25 RNA-sequencing analysis further reveals that stripe and interstripe iridophores have different transc

26 onal, we show how the landscape of competing stripe and magnetic phases can be addressed on a first-p

27 tron-scattering experiments that reveal both stripe and Neel spin fluctuations over a wide energy ran

28 es in a system exhibiting competing magnetic stripe and skyrmion phase using a soft X-ray speckle met

29 daries and underlying critical points in the stripe and skyrmion phases.

30 patterns, and we use our methods to predict stripe and spot statistics as a function of varying cell

31 titatively recapitulate the formation of the stripe and that control of the window of time over which

32 hat frustration of the otherwise dominant Fe stripe and V Neel fluctuations via interfacial coupling

33 atterned expression of Alx3 precedes pigment stripes and acts to directly repress Mitf, a master regu

34 te the formation of diffuse clones, chimeric stripes and belly spots.

35 entified peaks are localized along extrusion stripes and form transitive grids, consistent with their

36 find that iridophores do not migrate between stripes and interstripes but instead differentiate and p

37 pe of iridophore migrating differentially to stripes and interstripes.

38 phological transformations involving nematic stripes and locally aligned focal conic domains.

39 The stripes and resulting frictional domains appear on monol

40 munities and controllable arrays of cellular stripes and spots in space.

41 rning is the zebrafish; its alternating blue stripes and yellow interstripes depend on light-reflecti

42 brane to permit stable, low-overpotential Mg striping and plating for over 100 cycles at a current de

43 e organic-inorganic interface (e.g., helical stripes), and the kernel.

44 gement, thickening of the right paratracheal stripe, and scattered patchy increased interstitial mark

45 of domain growth and the initial iridophore stripe, and to generate hypotheses about the functions o

46 distribute their outputs to the different V2 stripes, and whether different stripes receive inputs fr

47 evealed an in-plane oriented diagonal double-stripe antiferromagnetic spin structure.

48 Architectural stripes appear to be driven by enhancer activity, becaus

49 ally the fastest, faster even than Farrar's 'striped' approach, however the opal library is faster fo

50 Furthermore, we show that architectural stripes are a frequent feature of developmental three-di

51 R) biosensors consisting of many rectangular stripes are being developed for high sensitivity medical

52 lt suggests that dynamic shifts of pair-rule stripes are essential for segment patterning in the trun

53 ent activity of five enhancers, even-skipped stripes are sculpted by the same kinetic phenomena: a co

54 netic phase, attesting that the canting spin stripes are three-fold degenerate states akin to helices

55 nsition temperature cuprate superconductors, stripes are widely suspected to exist in a fluctuating f

56 ion, the olivary inputs to the ZII+ and ZII- stripes arise from different, although adjacent, regions

57 We asked whether V1 inputs to different V2 stripes arise from morphologically different cell types.

58 Here, we show that a model of the tiger stripes as tidally flexed slots that puncture the ice sh

59 g an axis orthogonal to the ocular dominance stripes, as recently demonstrated in cats.

60 We confirm that the nine stripes ascribed to myosin binding protein-C are not rel

61 In a stripe assay, however, where M1-4 lanes alternate with p

62 bserved during the polarization of HUVECs in stripe assays.

63 Here, by removing dpp from the stripe at different time points, we show that the dpp st

64 ion included a blue stripe in place of a red stripe at the right-hand end of the scale.

65 l area (V2) in non-human primates contains a stripe-based anatomical organization, initially defined

66 al MRI (7T), we provide in vivo evidence for stripe-based subdivisions in humans.

67 We revealed stripe-based subdivisions in V2 ending at the V1/V2 bord

68 ng evidence for functional organization into striped-based subdivisions in human V2 and V3.

69 Behavioural adaptions to weather events by striped bass and other coastal fishes will depend on mai

70 for tilapia, catfish, trout, salmon, hybrid striped bass and yellow perch, respectively.

71 Striped bass moved out of the estuary, exhibiting novel

72 idin 1 (P1), isolated from the mast cells of striped bass, has potent activities against bacteria, vi

73 The stripes become dynamic at high temperatures, but LSNO re

74 and, crucially, that prey with high-contrast stripes become less visible than prey with background-ma

75 Thick stripes best coded for lower spatial frequencies and hig

76 struction and rules out criss-crossed charge stripes between layers as a viable alternative in Hg1201

77 stic domain walls in manganites induced by a stripe BiFeO3 template can modulate the electronic trans

78 als features consistent with the left dorsal stripe, black leading edges on the dorsal surfaces of th

79 sufficient to induce myosin accumulation at stripe boundaries.

80 ch cell types project to both thin and thick stripes, but one type, the giant spiny-stellate neuron,

81 t entopallium (E), an overlaying nidopallial stripe called intermediate nidopallium (NI), and the dor

82 We show that stripes can reduce the detection of moving prey by explo

83 Both the pseudogap and the stripe charge order disappear when the band is either em

84 ve a pseudogap phase accompanied by a global stripe charge order that breaks the rotational symmetry

85 s are formed in Pb films as modulated by the stripe charge order.

86 The two stripe/column types were largely interdigitated (e.g., n

87 s and can take the shape of highly organized stripes, convoluted beads, or no pattern at all.

88 Carlo calculations to demonstrate dynamical stripe correlations in the three-band Hubbard model, whi

89 spectrum built on short-range, quasi-static, stripe correlations.

90 and morphogenetic behaviors is necessary for stripe development.

91 ical junction is controlled by the change in stripe direction, while the torsion angle defined by eac

92 Verticillium stem striping disease on oilseed rape was mainly observed in

93 in lattice anisotropy while maintaining the stripe domain morphology with 109 degrees domain wall.

94 transforms into the less-symmetric parallel-stripe domain structure, before the onset of paraelectri

95 rved with relatively short range-ordering of stripe domains due to the modified electrostatic boundar

96 that the unique topological configuration of stripe domains represents a permissive landscape facilit

97 10 GHz is observed and propagates along the stripe domains with a spin-wave dispersion different fro

98 vestigate spin waves in periodic 100-nm-wide stripe domains with alternating upward and downward magn

99 By tracking the developmental dynamics of stripe domains, we show that stripe formation is linked

100 n controllably modify the orientation of the stripe domains, which opens up perspectives for reconfig

101 r labyrinthine pattern, featuring meandering stripe domains.

102 We reveal locally unidirectional striped domains as small as 5 nm, despite apparent bidir

103 Such 'stripe' domains are associated with both poised and acti

104 with distinct regulatory features including stripes, dots, and domains linking promoters-to-promoter

105 the responses of these insect predators to a striped dummy target are reduced when the target is movi

106 The distal early stripe element (DESE) mediates both activation and repre

107 The proximal early stripe element (PESE) is also repressed by Runt, but in

108 In conclusion, V2 CytOx stripes exhibit a mixed degree of segregation and integr

109 milar color-selective or disparity-selective stripes exist in human V2.

110 ll and high-temporal resolution as its seven stripe expression pattern forms, and developed tools to

111 E-P stripes extending from the edge of domains predominantly

112 We show that the striped fibrillar pattern cannot be easily predicted fro

113 This striped fibrillar pattern is preserved across the animal

114 wth, further worsening the local hypoxia and striped fibrosis surrounding the CDs.

115 rsting nuclei from the posterior to anterior stripe flanks.

116 tal dynamics of stripe domains, we show that stripe formation is linked to the functional state of th

117 ch may lead to collective behaviour, such as stripe formation, as well as the microscopic exploration

118 cribes even-skipped plays a critical role in stripe formation.

119 or the wavelength of the periodic pattern of stripes formed by the logs and for the log diameter are

120 responsible for an adult trait of zebrafish, stripe-forming mechanisms also provide a conceptual fram

121 icial superlattice method in synthesizing 1D stripes from 2D layered materials.

122 spectroscopy performed on a red-blue-purple striped glass from the stained glass windows of the Sain

123 ce ordering of charge into a quasi-2D charge stripe ground state.

124 ith half-pitch of 6.4 nm are demonstrated on stripes >80 nm wide.

125 onents of such a condensate, the presence of stripes has not been detected.

126 Neurons in these stripes have been proposed to serve distinct functional

127 Vertical stripes have long been known to attract laboratory fruit

128 lular matrix with alternating soft and stiff stripes improves current NMJ-in-a-dish models by inducin

129 in ageing/disease regulation included a blue stripe in place of a red stripe at the right-hand end of

130 ty (N = 190 single units) across distinct V2 stripes in anesthetized and paralyzed capuchin monkeys (

131 jections to distinct cytochrome oxidase (CO) stripes in area V2: neurons in CO blob columns project t

132 ne Drosophila PRG orthologs are expressed in stripes in Dermestes Functional results parse these gene

133 These optokinetic zones relate to the ZII stripes in folium IXcd of the flocculus, such that an op

134 rcuits of L4B neurons projecting to V2 thick stripes in macaque.

135 stance signaling between the cells that make stripes in the adult zebrafish.

136 ity involves destabilizing insulating charge stripes in the doped Hubbard model.

137 ltus Seven Of-PRG-orthologs are expressed in stripes in the primordia of every segment, rather than e

138 metastatic melanoma cells avoid DAN protein stripes in vitro.

139 ed the sudden emergence of Verticillium stem striping in the UK, whereas in continental Europe Vertic

140 , selectively propagate from boundaries into stripe interiors (whereas horizontal lamellae form on th

141 The incidences of acute mild arteriolopathy, striped interstitial fibrosis, glomerular congestion, an

142 null allele, one study proposed that the dpp stripe is critical for patterning but not for growth.

143 r study proposed that Dpp dispersal from the stripe is required for patterning and also for medial wi

144 n factor concentrations, suggesting that the stripe is shaped by the interplay of 2 distinct underlyi

145 lices and the multiple state of canting spin stripes is a circular configuration with zero skyrmion c

146 he 10(6)-y average power output of the tiger stripes is buffered by a feedback between ice melt-back

147 reas in continental Europe Verticillium stem striping is predominantly caused by the more genetically

148 F231(K1), and F234(K1)), the K10 hydrophobic stripe, K1 interaction residues, and the C-terminal anch

149 tly image Neel-type skyrmion lattice and the stripe-like magnetic domain structures as well.

150 ombined presence of nematic and 'smectic' or stripe-like orders seen in recent scanning tunneling mic

151 ment, WntA is necessary for the induction of stripe-like patterns known as symmetry systems and acqui

152 arch, a basal nymphalid butterfly that lacks stripe-like symmetry systems.

153 EASE, DWD-HYPERSENSITIVE-TO-ABA3, and YELLOW STRIPE-LIKE5) were further studied by reverse genetics,

154 ugar maple, yellow birch, cordate birch, and striped maple.

155 Here, we propose the dot-stripe mechanism for joint patterning, comprising two co

156 Other phonons are a lot less sensitive to stripe melting.

157 Using stripe migration assays, chimeric cell-cell fusion assay

158 By formulating a generic dot-stripe model, describing joint patterns rather than mole

159 n of collagen-like filaments of well-defined striped morphologies.

160 demonstrates that the four-component barley stripe mosaic virus-based system allows the overexpressi

161 Here, a four-component barley stripe mosaic virus-based system with high cargo capacit

162 activity of individual nuclei, we show that stripe movement is driven by the exchange of bursting nu

163 range ordering of ferroelectric 109 degrees stripe nanodomains separated by periodic vertical domain

164 Additionally, thin stripe neurons continued to increase their firing rate f

165 e, a magnetic phase composed of canting spin stripes, never observed in the chiral magnets, forms.

166 Striped NPls were observed in the final products, due to

167 es close to the periodicity and width of the stripes observed in continuous films.

168 ing reduced levels of Ihog/Boi proteins in a stripe of cells at the anterior/posterior compartment bo

169 morphogen gradient derived from the anterior stripe of cells is thought to control growth and pattern

170 -mesenchymal-like transition of a continuous stripe of cells that sweeps across the neuroepithelium,

171 Thus, the stripe of Dpp ensures that signalling remains above a pr

172 sified recently with the suggestion that the stripe of Dpp is dispensable for growth.

173 conditional alleles of dpp, we find that the stripe of Dpp is essential for wing growth.

174 revealed mature principal cells in the inner stripe of the outer medulla converted to intercalated ce

175 Transcription begins as a narrow stripe of two or three cells along the ventral midline,

176 ith features of the filament, such as the 11 stripes of accessory proteins.

177 visual cortex, different cytochrome oxidase stripes of area V2 receive segregated projections from l

178 allel pathways which terminate into distinct stripes of area V2.

179 While some systems exhibit stripes of charge and spin, with a locked periodicity, o

180 lished by a Turing-like mechanism generating stripes of chondrogenic domains.

181 Distinctive "thin" and "thick" stripes of dark CO staining reportedly respond selective

182 ibroblasts on substrates micropatterned with stripes of fibronectin and observed that contact guidanc

183 nje cells (PCs) such that there are sagittal stripes of high expression (ZII+) interdigitated with st

184 f high expression (ZII+) interdigitated with stripes of little or no expression (ZII-).

185 spatial patterns of gene expression, such as stripes of macrophages expressing arginase 1 (ARG1) and

186 ly anisotropic in-plane structures featuring stripes of metallic TaTe(2) and semiconducting FeTe(2),

187 g produces alternating positive and negative stripes of PCs across most of the cerebellar cortex.

188 Moreover, ectopic stripes of Tartan and Ten-m are sufficient to induce myo

189 , the FLP proved to be capable of completely striping-off hydrogen and hydrides to generate the first

190 ter medullary collecting duct from the inner stripe (OMCDi) is not known.

191 undaries are formed at the edges of isolated stripes on a background substrate.

192 to ensure a reducing glass matrix in the red stripe or a metastable overoxidized glass in the purple

193 at, infinite sheet, the patterns are uniform striped or hexagonal.

194 erns have a richer phenomenology than simple stripes or hexagons.

195 anics of epithelial cell aggregates-islands, stripes, or entire monolayers-that combines both vertex

196 two types of CDW orders in LSCO, namely CDW stripe order and CDW short-range order (SRO).

197 This indicates that stripe order at low temperatures is stabilized by the co

198 The favored filled stripe order is different from that seen in real materia

199 nto the CDW stripe order with developing SDW stripe order near the superconducting T(c).

200 We find a stripe order that has a highly compressible wavelength o

201 SC, it is partially transformed into the CDW stripe order with developing SDW stripe order near the s

202 spin component, keeping the diagonal double-stripe order.

203 We report on the magnetism of charge-stripe ordered La(2)NiO(4.11+/-0.01) by neutron scatteri

204 tion of charge correlations in the canonical stripe-ordered cuprate La1.875Ba0.125CuO4 across its ord

205 m transport measurements on charge- and spin-stripe-ordered La(1.7)Eu(0.2)Sr(0.1)CuO(4) and La(1.48)N

206 of these ideas to the recent experiments on stripe-ordered La(1.875)Ba(0.125)CuO(4) (LBCO) are discu

207 Here, we employ resonant x-ray scattering in stripe-ordered superconductors (La,M)2CuO4 to probe the

208 These findings indicate that the stripe orders and SC are inhomogeneously distributed in

209 occulus insofar as the CSA of all PCs in the stripe pair encodes similar sensory information, the oli

210 Thus, although a ZII+/- stripe pair represents a functional unit in the pigeon f

211 airs, whereas the VA zones correspond to ZII stripe pairs P4+/- and P6+/-.

212 r: the HA zones span the P5+/- and P7+/- ZII stripe pairs, whereas the VA zones correspond to ZII str

213 hat the French Angelfish (Pomacanthus paru), Striped Parrotfish (Scarus iseri), Rock Beauty (Holacant

214 g studies suggest that V2 cytochrome oxidase stripes participate in functionally distinct streams of

215 ral crest derived pigment cells of the adult stripe pattern, limiting melanophore population expansio

216 ntrast within gray matter, we also observe a stripe pattern.

217 Adult zebrafish exhibit a striking striped pattern generated through the self-organisation

218 g these issues, we investigated the periodic striped patterning of the rugae (transverse ridges) in t

219 -assemble into fibrils of well-defined axial striped patterns.

220 /Li-C symmetric cell exhibits stable plating/striping performance with small voltage hysteresis and e

221 abrupt magnetic domain jumps observed in the stripe phase are dramatically reduced in the skyrmion ph

222 zed by confinement and a spatially modulated stripe phase is predicted at the A-B phase boundary.

223 f the breathing modes indicates that dynamic stripe phase may host small polarons.

224 rve the predicted density modulation of this stripe phase using Bragg reflection (which provides evid

225 The stripe phase we have detected is accompanied by short-ra

226 in-orbit coupling are predicted to possess a stripe phase with supersolid properties.

227 , with implications for the stability of the stripe phase.

228 nd Ni appears on entering the dynamic charge stripe phase.

229 is simple model, featuring a broken-symmetry striped phase that is disrupted at both high and low ext

230 In YBa(2)Cu(3)O(7), we find many stripe phases that are nearly degenerate with the ground

231 material with charge-order transitions into stripe phases.

232 ganisms exhibit visually striking spotted or striped pigmentation patterns.

233 The human stripes reach into V3.

234 neurons in male macaques, we show that thick stripes receive a greater contribution of L4B inputs fro

235 different V2 stripes, and whether different stripes receive inputs from morphologically distinct neu

236 rs swing upwards or downwards in alternating stripes, reflecting the spin-ice symmetry of the static

237 These stripes represent an intermediate stage in visual hierar

238 nd ventral streams via the V2 thick and thin stripes, respectively.

239 s have alternating dark and light horizontal stripes, resulting from the precise arrangement of three

240 mes 2M and 7M of Ae. comosa might harbor new stripe rust and powdery mildew resistance genes, respect

241 id or with the avirulent race, CYR23, of the stripe rust pathogen Puccinia striiformis f.

242 ng of YrAS2388R will facilitate breeding for stripe rust resistance in wheat and other Triticeae spec

243 Wheat stripe rust, caused by Puccinia striiformis f. sp. triti

244 Wheat stripe rust, due to infection by Puccinia striiformis f.

245 t of novel strategies for durable control of stripe rust.

246 to various diseases including leaf rust and stripe rust.

247 , the entrance of Pb(2+) ions generated PbSe stripes "sandwiched" in between hexagonal Cu2Se domains.

248 trilayer samples consisting of rigid plastic stripes sandwiching a swellable temperature-responsive h

249 -valve (GMR SV) biosensor array with a multi-stripe sensor geometry and matched filtering to improve

250 e monolayer is observed with parallel linear stripes separated by a distance of 3.8 nm corresponding

251 th our ready-to-use computational workflows, STRIPE-seq is a straightforward, efficient means by whic

252 ion of uncapped RNA and reaction cleanups, a STRIPE-seq library can be constructed in about 5 h.

253 We show application of STRIPE-seq to TSS profiling in yeast and human cells and

254 er Elements with high-throughput sequencing (STRIPE-seq), a simple, rapid, and cost-effective protoco

255 process for outputting data, the mainstream stripe-shaped concept certainly suffers from the data ov

256 Stripe-shaped contact patterns-anchored by CTCF-grow in

257 If so, available evidence predicts that such stripes should (1) radiate "outward" from the V1-V2 bord

258 Thin stripes showed the highest proportion (80%) of neurons s

259 area MT, was only found to project to thick stripes.SIGNIFICANCE STATEMENT Area V1 partitions visual

260 ng the observation of cytopathic effect in a striped-snakehead fish cell line, 35-nm virions with fla

261 different time points, we show that the dpp stripe source is indeed required for wing disc growth, a

262 Stripe subdivisions preferentially responding to fast te

263 and are pinned by chemical contrast at each stripe/substrate boundary, align parallel to boundaries,

264 tside blob columns project to thick and pale stripes, suggesting functional specialization of V1-to-V

265 f urbanization, for three bee species: silky striped sweat bees (Agapostemon sericeus), western honey

266 lag, and the total power output of the tiger stripe terrain, while suggesting that eruptions are main

267 d as well as a smooth transition from single stripe to bubble domains, which opens the door to future

268 onal burst frequency is modulated across the stripe to control the mRNA production rate.

269 orm on the background), and register to wide stripes to multiply the feature density.

270 provided with educational interventions-the STRIPES trial).

271 ly order volume fraction is 87% from the two stripe twins, and the temperature evolution of the magne

272 Both stripe types, however, receive a much larger contributio

273 e seen in chromium metal than the insulating stripes typically found in single-layer nickelates like

274 silencing suppressor protein encoded by Rice stripe virus (RSV), a negative-strand RNA virus.

275 risea, Xanthomonas oryzae pv.oryzae and rice stripe virus were analyzed.

276 s pigmented) that we identify as the "medial stripe" visible in many rachis-dominated rectrices of Me

277 , while chicks failed to spontaneously use a striped wall in a square arena, rats showed a modest inf

278 The critical third experiment tested the striped wall inside the rectangular arena.

279 ks, using a single prominent featural cue (a striped wall) within a rectangular arena.

280 Also, 8 different types of sensor stripes were fabricated and design parameters were explo

281 ecific-FGF signalling were incorporated once stripes were formed.

282 These stripes were originally taken as evidence of the directe

283 th technique BSFs are bunched up in parallel stripes where the lower wavelength peak is broadened and

284 g both mouse and human myoblast durotaxis to stripes where they aligned, differentiated, and fused in

285 ast patterns with repeated elements, such as stripes, which are highly visible when prey are stationa

286 rom M-dominated stellates compared with thin stripes, which project to areas processing object attrib

287 We find that V2 thick stripes, which project to areas processing object motion

288 tually patterned as evenly spaced spots, not stripes, which then elongate into rod-shaped digit rays

289 : neurons in CO blob columns project to thin stripes while neurons outside blob columns project to th

290 on between eccentricity and ocular dominance stripe width.

291 nd observed that contact guidance emerges at stripe widths much greater than the cell size.

292 regimes of contact guidance: 1) guidance on stripe widths smaller than the cell size (w <= 160 mum),

293 ongation; and 2) entropic guidance on larger stripe widths, which is governed by fluctuations in the

294 reducing the gap width between the magnetic stripes will enable controlled manipulation of individua

295 many warning signals combine black spots and stripes with a lighter colour such as yellow.

296 rbates into a highly regular superlattice of stripes with period 4-6 nm.

297 ., proportionally wide rachis with a "medial stripe") with lithic, two-dimensionally preserved rachis

298 selectivities compared to the thick and thin stripes, with relatively stronger coding for orientation

299 or olive (mcIO) project to the ZII+ and ZII- stripes within each of the functional pairs.

300 mine the olivary inputs to the ZII+ and ZII- stripes within the functional pairs.