ライフサイエンスコーパス: stripe

1 >15 kHz correlates with the loss of Hensen's stripe.

2 metastable overoxidized glass in the purple stripe.

3 sor signals over those located on the sensor stripes.

4 that reduces the Coulomb repulsion among the stripes.

5 ristic pattern of golden and blue horizontal stripes.

6 pair-rule' genes, each in a pattern of seven stripes.

7 n the form of partially disordered nanoscale stripes.

8 rms wrinkles perpendicular to the underlying stripes.

9 the distribution of magnetic labels over the stripes.

10 light stripes and the loose form of the dark stripes.

11 ating excitatory and inhibitory parasagittal stripes.

12 signal due to magnetic labels between sensor stripes.

13 re located in lateral P1- and medial P2+ ZII stripes.

14 nd long particle-jets from the tips of these stripes.

15 sponses to optic flow visual stimuli and ZII stripes.

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

17 oping in terms of the physics of fluctuating stripes.

18 anophores from coalescing into adult pigment stripes.

19 their spins organize into patterns known as stripes.

20 are mainly responsible for Verticillium stem striping.

21 and a sequence encompassing the minimal eve stripe 2 enhancer (eve2+7).

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

23 The eve stripe 2 transgene exhibits a highly dynamic pattern of

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

25 unctionally regulates the even-skipped (eve) stripe 3+7 enhancer (eve3+7) in Drosophila blastoderm em

26 +7 enhancer could not explain endogenous eve stripe 7 behavior.

27 Instead, we found that eve stripe 7 is controlled by two enhancers: the canonical e

28 Hb bifunctionally regulates eve stripe 7, but it executes these two activities on differ

29 plausibly the major energy source for tiger stripe activity.

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

31 Fruits of Xylopia parviflora, well known as striped African pepper, are sold in the Cameroonian mark

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

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

34 REV1 enrichment at DNA damage stripes also partially depends on BRCA1 and BRCA2, compo

35 ABAergic, was located primarily in the dbx1b stripe and also had contralateral projections terminatin

36 analyze the signal from both a single sensor stripe and an array of sensor stripes as function of the

37 our different dynamical mechanisms to form a stripe and identify the minimal network of each group.

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

39 r stripes that interdigitated with the SAX-7 stripe and PVD dendrites, reflecting the striking precis

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

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

42 located in interstripes and thin CytOx-rich stripes and avoided the CytOx-rich thick stripes in V2.

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

44 y towards the quantitative theory of dynamic stripes and for directly detecting dynamical charge stri

45 projections were located in CytOx-rich thin stripes and in the CytOx-poor interstripes, whereas the

46 nerated by geometric patterns of impermeable stripes and investigate their potential to regularize el

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

48 his technique has been used to remove charge stripes and promote superconductivity, acting in a way o

49 al cells, which in turn instructed the SAX-7 stripes and PVD dendrites.

50 The stripes and resulting frictional domains appear on monol

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

52 witching between the dense form of the light stripes and the loose form of the dark stripes.

53 V2 stripes and V3 columns were reliably localized in all su

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

55 mcIO were located in lateral P2+ and P2- ZII stripes, and climbing fibers from the middle lateral mcI

56 henotypes such as multiple stripes, inverted stripes, and gradients of gene expression.

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

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

59 ted for an implementation based on Farrar's 'striped' approach.

60 uctures possessing core/shell, segmented, or striped architectures.

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

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

63 In sbr mutants, the dark stripes are interrupted by dense iridophores invading as

64 ctuations associated with the dynamic charge stripes are narrow in q and broad in energy.

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

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

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

68 etching can be used to fabricate the arched stripe arrays.

69 single sensor stripe and an array of sensor stripes as function of the geometrical parameters of the

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

71 of the geometrical parameters of the sensor stripes as well as the distribution of magnetic labels o

72 s almost all observers to report the lighter stripes as yellowish.

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

74 bserved during the polarization of HUVECs in stripe assays.

75 amatergic class was medially located along a stripe associated with the alx transcription factor; the

76 gic class was more laterally located along a stripe associated with transcription factor dbx1b; these

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

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

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

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

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

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

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

84 l evacuations by otherwise resident riverine striped bass in the Hudson River Estuary, New York, USA,

85 Striped bass moved out of the estuary, exhibiting novel

86 ther than by the labels on top of the sensor stripes because these are at a lower height.

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

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

89 cription factors responsible for forming the stripe boundaries of the studied genes.

90 Lipids from striped catfish muscle were extracted with the aid of cr

91 ensions, we were able to create circular and striped cellular patterns.

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

93 mcIO were located in P1+ and medial P1- ZII stripes; climbing fibers from the rostral lateral mcIO w

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

95 sent a diblock copolymer system exhibiting a striped columnar phase that preferentially forms wrinkle

96 ly alike (compared with functionally unlike) stripes/columns in V2 and V3.

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

98 tical lattice fluctuations, driven by charge-stripe correlations, in La2-xSrxNiO4 using inelastic neu

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

100 ely structural order parameter in underdoped striped cuprates.

101 olium IXcd consists of seven pairs of ZII+/- stripes denoted P1+/- (medial) to P7+/- (lateral).

102 Color-selective stripes differed from disparity-selective stripes in bot

103 retical proposals of dynamically fluctuating stripes, direct spectroscopic evidence of charge-stripe

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

105 A solution to the riddle of zebra stripes, discussed by Wallace and Darwin, is at hand.

106 delphax striatellus, and causes serious rice stripe disease.

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

108 152) cetaceans, three out of four species:- striped dolphins (SDs), bottlenose dolphins (BNDs) and k

109 Six animals (5 striped dolphins and 1 common dolphin) showed IHC and/or

110 ificantly with body size for both common and striped dolphins.

111 esviral DNA in brain tissue samples from two striped dolphins.

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

113 genetically removing Dpp from its endogenous stripe domain, we confirm the requirement of Dpp for the

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

115 ization associated with 125 nm-wide magnetic stripe domains in 100-nm-thick Ni films.

116 As for the size effect of 180 degrees stripe domains in ferroelectric thin films, there have b

117 at the domain periodicity (w) of 180 degrees stripe domains scales with the film thickness (d) accord

118 onstrated current-driven transformation from stripe domains to magnetic skyrmion bubbles could lead t

119 ansition, inducing preferential formation of striped domains along the terraces of atomically flat st

120 We reveal locally unidirectional striped domains as small as 5 nm, despite apparent bidi

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

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

123 lar, highly structured and unexpected 'zebra stripes', even when the solar-wind activity is low.

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

125 y and that members of this subfamily exhibit striped expression (as seen in Tribolium and previously

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

127 Observations show eruptions from "tiger stripe" fissures that are sustained (although tidally mo

128 pes, direct spectroscopic evidence of charge-stripe fluctuations has been lacking.

129 nally test every possible 3-node network for stripe formation in a morphogen gradient.

130 leles demonstrate that luchs is required for stripe formation in zebrafish; however, the fins are alm

131 -mixing, including microphase separation and stripe formation.

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

133 minent pattern of alternating dark and light stripes generated by the precise positioning of pigment

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

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

136 e study, we cloned 643 bp RFRP cDNA from the striped hamster hypothalamus, which contained an ORF of

137 RFRP-3 on the reproductive activity for the striped hamster is less understood.

138 a century of interest, the function of zebra stripes has never been examined systematically.

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

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

141 otts antiferromagnet at low densities to the striped herringbone phase of planar quadrupoles at highe

142 atches the width of the partially disordered stripes, implying a connection between the structural ph

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

144 REV1 is targeted to laser-induced DNA damage stripes in a manner dependent on its ubiquitin-binding m

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

146 ve stripes differed from disparity-selective stripes in both width (thickness) and length.

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

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

149 The charge stripes in La-438 are weakly correlated along c to form

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

151 and for directly detecting dynamical charge stripes in other strongly correlated systems, including

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

153 ich stripes and avoided the CytOx-rich thick stripes in V2.

154 metastatic melanoma cells avoid DAN protein stripes in vitro.

155 We show that stripes in zebrafish require a novel class of thin, fast

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

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

158 to evolve novel phenotypes such as multiple stripes, inverted stripes, and gradients of gene express

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

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

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

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

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

164 Recent experiments indicate that static stripe-like charge order is generic to the hole-doped co

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

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

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

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

169 aramagnet interpolating between the Neel and stripe magnetic instabilities.

170 on-pnictide superconductors exhibit Neel and stripe magnetic order, respectively.

171 lightly above, the ordering temperature of a stripe magnetic phase.

172 ch, particularly those near the edges of the stripes, mainly affect the sensor signals due to additio

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

174 cells that mediate regeneration of zebrafish stripe melanocytes and defined how these cells reconstit

175 tions through the oxalate-bridges suggests a stripe mode pattern of coupling with weak ferromagnetic

176 Barley stripe mosaic virus (BSMV)-mediated over-expression of b

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

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

179 Here we show that, in the African striped mouse (Rhabdomys pumilio), periodic dorsal strip

180 outh-polar terrain, informally called 'tiger stripes', named Alexandria, Baghdad, Cairo and Damascus

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

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

183 raining data contain a significant amount of striping noise.

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

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

186 e the patterning role of Dpp secreted from a stripe of cells along the anterior-posterior compartment

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

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

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

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

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

192 tation of a morphogen gradient into a single stripe of gene expression as a model phenotype.

193 rcuit topologies that can robustly develop a stripe of gene expression, the vast majority of these ci

194 odelling and axis elongation, and an ectopic stripe of Toll receptor expression is sufficient to indu

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

196 nciples of animal coat patterns, such as the stripes of a tiger, great effort has been made to unders

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

198 Moreover, Alx3 is upregulated in the light stripes of chipmunks, which have independently evolved a

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

200 ith chondroitinase improved GRP migration on stripes of CSPG printed on cover glass, although GRPs we

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

202 the reconstruction consists of self-aligned stripes of enhanced atom density formed to relieve the t

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

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

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

206 t-cell autonomous interactions generate dark stripes of melanophores that alternate with light inters

207 In assays involving alternating stripes of monospecific matrices, human control GCs exhi

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

209 Here we match variation in striping of equid species and subspecies to geographic r

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

211 e SAX-7/L1CAM, which formed regularly spaced stripes on the hypodermal cell.

212 s, which self-organize into five ripple-like stripes on the surface of the barrel-shaped Au105 kernel

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

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

215 on produce differently shaped solid domains (striped or irregular hexagons), shift fluid-solid transi

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

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

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

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

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

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

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

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

224 le slopes the typical pattern form is bands (stripes), oriented parallel to the contours, and their w

225 The bright colour of the limpet's stripes originates from light interference in a periodic

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

227 Taken together, we suggest that a ZII+/- stripe pair may represent a functional unit in the pigeo

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

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

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

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

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

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

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

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

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

237 material with charge-order transitions into stripe phases.

238 with a diameter of 50 nm located between the stripes predominantly determine the sensor signals over

239 tion from magnetic labels between the sensor stripes rather than by the labels on top of the sensor s

240 The human stripes reach into V3.

241 The stripes' reflection band coincides with the spectral ran

242 s of DOPC and cholesterol exhibit large-area striping reminiscent of the stripe superstructures that

243 These stripes represent an intermediate stage in visual hierar

244 d mouse (Rhabdomys pumilio), periodic dorsal stripes result from underlying differences in melanocyte

245 Here we use observed and modelled data on stripe rust occurrence to gauge changes in the geographi

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

247 eny analysis to map the Yr6 locus for yellow stripe rust resistance in hexaploid wheat.

248 ch investment of at least US$32 million into stripe rust resistance is economically justified.

249 ment a significant increase in the spread of stripe rust since 1960, with 88% of the world's wheat pr

250 esistant varieties of wheat with the cost of stripe-rust-induced yield losses, we estimate that a sus

251 Comparing the cost of developing stripe-rust-resistant varieties of wheat with the cost o

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

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

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

255 l point as shown by characteristic circle-to-stripe shape transitions.

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

257 s monolayer, which first forms periodic wavy-stripe-shaped transverse density modulation in the monol

258 sensitive to human antidepressant drugs; the striped shore crab, Pachygrapsus crassipes, was studied

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

260 w banded 'postman' wing pattern in the tiger-striped silvaniform clade, and co-mimetic H. melpomene n

261 Results suggested that striped skunks (Mephitis mephitis) can successfully tran

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

263 se compounds, superconductivity emerges when stripe spin density wave (SDW) order is suppressed by do

264 g-by neutron scattering, finding substantial stripe spin fluctuations coupled with the nematicity tha

265 l weight is transferred from the Neel to the stripe spin fluctuations.

266 enes, extramacrochaetae (emc), hairy (h) and stripe (sr), involved in repression have been documented

267 more compact hexagonal close packed quasi-1D stripe structure.

268 Stripe subdivisions preferentially responding to fast te

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

270 The charge stripe superlattice propagation vector, q = (2/3, 0, 1),

271 We show that the stripe-superlattices can be reproducibly and reversibly

272 hibit large-area striping reminiscent of the stripe superstructures that characterize the proximity o

273 y and topological defects in crystalline and striped systems.

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

275 k projections were more abundant in the thin stripes than in the interstripes.

276 esmosome components exhibited highly regular stripes that interdigitated with the SAX-7 stripe and PV

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

278 provided with educational interventions-the STRIPES trial).

279 sor signals due to additional field from the stripe under an applied field.

280 d that Ca(2+) channels remained clustered in stripes underneath anchored ribbons.

281 Rice stripe virus (RSV) is known to be transovarially transmi

282 In patterned FeRh stripes we observed pronounced supercooling and an avala

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

284 These stripes were originally taken as evidence of the directe

285 The C-terminal antibody stripes were slightly displaced axially, demonstrating a

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

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

288 ortex (V2) is composed of repeating columnar stripes, which are evident in histological variations of

289 ve shell ensures the vivid shine of the blue stripes, which can be perceived under water from a wide

290 y distorted by a charge modulation on the Mn stripes, which in turn drives an unusually large displac

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

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

293 oach based on a DUV LED having multiple mesa stripes whose inclined sidewalls are covered by a MgF2/A

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

295 We show that the signal from sensor stripes with a uniform protective coating, contrary to c

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

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

298 rprisingly, however, we find that the charge stripes within each trilayer of La-438 are stacked in ph

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

300 al pigment cell classes interact to generate stripes, yet the developmental requirements and origins