ライフサイエンスコーパス: pattern formation

1 ays a role in developmental decisions during pattern formation.

2 nd survival is an essential prerequisite for pattern formation.

3 lular and molecular basis of feather pigment pattern formation.

4 biophysical studies of self-organization and pattern formation.

5 tion and inhibition processes drives spatial pattern formation.

6 um is characterized by two distinct waves of pattern formation.

7 riptional networks change dynamically during pattern formation.

8 or investigating mechanisms of developmental pattern formation.

9 ich these influences are required for normal pattern formation.

10 fundamental physics controlling the complex pattern formation.

11 xis in producer-scrounger groups can lead to pattern formation.

12 on by Ral during cell fate specification and pattern formation.

13 e to the developmental control of growth and pattern formation.

14 table activator gradient to robustly control pattern formation.

15 hormone essential for plant development and pattern formation.

16 descendants play an important role in axial pattern formation.

17 ies and how the resulting system facilitates pattern formation.

18 hereby guiding future studies of neocortical pattern formation.

19 ient dynamics in a growing tissue to precise pattern formation.

20 cult to implement or they preclude arbitrary pattern formation.

21 nism formulation and guide future studies of pattern formation.

22 essential for polarized and continuous vein pattern formation.

23 fforts have been made to explain the dynamic pattern formation.

24 er, it is not known how DRG11 contributes to pattern formation.

25 receptor-mediated signaling to ensure robust pattern formation.

26 l for cellularization, sex determination and pattern formation.

27 nd we investigated the role of Notch in lung pattern formation.

28 nal epithelial polarity and retinal cellular pattern formation.

29 ne of the best-studied examples of embryonic pattern formation.

30 (GRPI) can guide systems-level approaches to pattern formation.

31 well-established paradigm for developmental pattern formation.

32 ntegration of convergent inputs for premotor pattern formation.

33 r responses that are necessary for embryonic pattern formation.

34 anism of soma/germline cooperation affecting pattern formation.

35 the same functions in controlling growth and pattern formation.

36 al axis, thus revealing a novel mechanism of pattern formation.

37 (TOAD2), required for Arabidopsis embryonic pattern formation.

38 milies act antagonistically during embryonic pattern formation.

39 l of Smad1 phosphorylations during embryonic pattern formation.

40 ty and spatial-temporal symmetry breaking of pattern formation.

41 vironment may regulate organ development and pattern formation.

42 urfaces and in the context of the absence of pattern formation.

43 tion depend crucially on the mitotic spindle pattern formation.

44 t to regulate growth of the eye disc but not pattern formation.

45 nt transport mechanisms or ;modules' control pattern formation.

46 d cells were dominant mechanisms of cellular pattern formation.

47 y, protein motors and bacterial motility and pattern formation.

48 imized drug synthesis and programmed spatial pattern formation.

49 especially when they occur during embryonic pattern formation.

50 roach to explore the molecular mechanisms of pattern formation.

51 cts growth and final size without disturbing pattern formation.

52 s pathway or fms requirements during pigment pattern formation.

53 or the reproducibility and robustness of the pattern formation.

54 explain experimentally observed dynamics of pattern formation.

55 quired for proper morphogenetic movement and pattern formation.

56 mputations, which have been shown to lead to pattern formation.

57 ilitates predictive-design of motility-based pattern formation.

58 s indispensable for organogenesis and tissue pattern formation.

59 d accounts for the precision and dynamics of pattern formation.

60 , such as BMP-4, play important roles in the pattern formation.

61 otemporal responses such as oscillations and pattern formation.

62 lped us understand the genetic mechanisms of pattern formation.

63 and chemistry combine to drive morphogenetic pattern formation.

64 plain various phenomena of self-assembly and pattern formation.

65 x), which may facilitate anthocyanin pigment pattern formation.

66 contractility followed by mechanical strain pattern formation.

67 ll, and what mechanistic principles underlie pattern formation?

68 In an influential model of pattern formation, a gradient of Sonic hedgehog (Shh) si

69 We show how this pattern formation ability, which is analogous to solutio

70 a qualitative and quantitative effect on the pattern formation, above a critical value that we determ

71 s identify Sdf1 as a key molecule in pigment pattern formation, adding to the growing inventory of it

72 both gene families are mutated suggest that pattern formation along the central-peripheral axis resu

73 gradient of nuclear Dorsal protein controls pattern formation along the dorsal-ventral axis.

74 ic mRNA injection, we obtained evidence that pattern formation along the entire AP axis of the Episyr

75 rmal ridge (AER) that are essential for limb pattern formation along the proximodistal (PD) axis.

76 and TOAD2 are redundantly required for both pattern formation along the radial axis and differentiat

77 gent property of the system is manifested in pattern formation among phenotypes within a chemical gra

78 vestigations both of population dynamics and pattern formation and appears to be natural to the obser

79 ific transcription factors are essential for pattern formation and cell differentiation processes in

80 retinoids, which are required for embryonic pattern formation and cell differentiation.

81 any developmental control genes critical for pattern formation and cell fate specification during the

82 nt system with which to study morphogenesis, pattern formation and cell proliferation in an epitheliu

83 differentiation, HetR, is necessary for both pattern formation and commitment of approximately every

84 aling pathway plays an essential role in the pattern formation and development of metazoan animals.

85 the genetic network that governs heterocyst pattern formation and differentiation.

86 that can produce scale invariance in spatial pattern formation and discuss examples of systems that s

87 ial of the system for genetically programmed pattern formation and distributed computing.

88 , providing a new approach for understanding pattern formation and dynamics in these systems.

89 etical framework to understand multicellular pattern formation and enables the wide-spread use of mat

90 ells of four different types--a microcosm of pattern formation and gamete specification about which o

91 c consequences of wnt activation: endodermal pattern formation and gene expression required suppressi

92 ul for elucidating fundamental mechanisms of pattern formation and how these mechanisms evolve.

93 s et al. (2014) makes the connection between pattern formation and intercellular communication by sho

94 quantitatively the experimental dynamics of pattern formation and maintenance for wild type and muta

95 embryogenesis require the ability to monitor pattern formation and morphogenesis in large numbers of

96 difications, could be adapted for studies of pattern formation and morphogenesis in other model organ

97 ng and ordering data from imaging studies of pattern formation and morphogenesis in three model syste

98 Pattern formation and morphogenesis require coordination

99 oliferation-dependent cell pattern underlies pattern formation and morphogenesis throughout the metaz

100 regulate cell cycle exit are critical during pattern formation and morphogenesis.

101 oping limb serves as a paradigm for studying pattern formation and morphogenetic cell death.

102 Mechanisms regulating CNS pattern formation and neural precursor formation are rem

103 ng from stem cell differentiation, embryonic pattern formation and organ regeneration to engineered c

104 ltiplicity of clathrin functions in cortical pattern formation and provide important insights regardi

105 long history as a model system for studying pattern formation and regeneration in single cells.

106 Pattern formation and self-organization are fascinating

107 ion among nonneural somatic tissues regulate pattern formation and serve as signals that trigger limb

108 These data reveal powerful novel controls of pattern formation and suggest a constructive model linki

109 orchestrate the development of mirror-image pattern formation and the consequent generation of ectop

110 egulator of cell shape changes during colour pattern formation and the first cytoplasmic protein impl

111 ption factor, Olig2, plays critical roles in pattern formation and the generation of motor neuron and

112 nterface between genes involved in male tail pattern formation and those responsible for function.

113 has been used as a model system for studying pattern formation and tissue development for more than 5

114 mportant role in the regulation of embryonic pattern formation and tissue morphogenesis.

115 Based on pattern formations and time series of populations, we fo

116 where Gli activators play the major role in pattern formation, and a gain of Hh signaling phenotype

117 ng a link between natural genetic variation, pattern formation, and adaptation.

118 associated with developmental processes and pattern formation, and downregulated transcripts involve

119 robust and accessible model for studying the patterning, formation, and expansion of epithelial tubes

120 ecause these and other mechanisms of regular-pattern formation are not mutually exclusive and can coe

121 ular mechanisms that control proximal-distal pattern formation are poorly understood.

122 Morphogenesis and pattern formation are vital processes in any organism, w

123 complexes can be explained as a spontaneous pattern formation arising from the competition between t

124 Pattern formation, as occurs during embryogenesis or reg

125 ll types, metabolic interdependence and even pattern formation, as the spacing of heterocysts along t

126 How these signalling peptides orchestrate pattern formation at a molecular level remains unclear.

127 wn sites, which enable actuation and wrinkle pattern formation at lower applied voltages.

128 e analysis of the mechanisms associated with pattern formation at the onset of gastrulation.

129 mergent network dynamics such as spontaneous pattern formation, bistability and periodic oscillations

130 Embryogenesis offers a real laboratory for pattern formation, buckling, and postbuckling induced by

131 The control of DNA methylation pattern formation by replication dependent and independe

132 rfusion-independent regulation of epithelial pattern formation by the vasculature during organ develo

133 Recent studies revealed that pattern formation by these graded signals depends on uni

134 present the first demonstration that Turing pattern formation can arise in a new family of oscillato

135 The results show that the pattern formation can be described by the identification

136 compact triangles to fractal flakes, and the pattern formation can be explained by the anisotropic gr

137 that have been widely applied to biological pattern formation, can be harnessed to instruct the refi

138 ce reconstruction in ionic crystals; and the pattern formation caused by phase transitions in metal a

139 ed to cell wall biogenesis, xylem and phloem pattern formation, cell cycle, hormone stimulus, and cir

140 la leg is a good model to study processes of pattern formation, cell death and segmentation.

141 e cell number during development, cerebellar pattern formation, cerebellar physiology, and the role o

142 l accounts for the key features of wild-type pattern formation, correctly predicts patterning defects

143 ying and near-universal principle of regular-pattern formation despite scant empirical evidence.

144 streaming occurs during stages 8-10A, while pattern formation determinants such as oskar mRNA are be

145 onsistent with predictions of spatiotemporal pattern formation driven by stochastic resonance).

146 the long-range control of tissue growth and pattern formation during animal development.

147 amental cell signaling system that regulates pattern formation during animal development.

148 pment suggests that MED13 and MED12 regulate pattern formation during Arabidopsis embryogenesis by tr

149 st a conserved role of the nervous system in pattern formation during blastema-based regeneration.

150 g and experiments, that nano/microstructural pattern formation during dealloying results from the int

151 tice in the Drosophila eye is a paradigm for pattern formation during development.

152 mulating that specific sterols have roles in pattern formation during development.

153 Drosophila embryo is a classic paradigm for pattern formation during development.

154 alling gradient that directs both growth and pattern formation during Drosophila wing disc developmen

155 ssential role in cellular specialization and pattern formation during embryogenesis and in tissue reg

156 ning in oogenesis and for anterior-posterior pattern formation during embryogenesis.

157 rabidopsis MED13) are required for timing of pattern formation during embryogenesis.

158 rmination in metazoans, contributing to both pattern formation during embryonic development and poste

159 in anterior Pn.p cells reflect mechanisms of pattern formation during normal hook development.

160 s are an important source of information for pattern formation during organogenesis.

161 rtance of positional information to instruct pattern formation during regeneration.

162 HEHD pattern formation enables the fabrication of multiscale

163 method, computations for surface diffusion, pattern formation, excitable media, and bulk-surface cou

164 e these data to build a theory on heterocyst pattern formation, for which both genetic regulation and

165 . obscuripes by shifting the drivers of nest pattern formation from an endogenous process (queen flig

166 hlight the multifaceted role of mechanics in pattern formation, from protein and cell sorting to the

167 and the ;ventral repression element' of the pattern-formation gene zerknullt.

168 selection acting on expression phenotype of pattern formation genes.

169 Growth factor signaling is essential for pattern formation, growth, differentiation, and maintena

170 One universal mechanism for the pattern formation has been long believed to be the misma

171 local-scale interactions driving large-scale pattern formation has been supported by numerical simula

172 fundamental physics governing the nanoscale pattern formation has not yet been identifed.

173 So far, studies into neural pattern formation have been restricted mainly to animal

174 ally test the hypothesis that self-organized pattern formation improves the persistence of mussel bed

175 Under these circumstances, pattern formation in a developing tissue involves a sele

176 Inter-regional signaling coordinates pattern formation in Arabidopsis thaliana embryos.

177 Pattern formation in biofilms allows cells to position t

178 Pattern formation in biofilms depends on cell proliferat

179 Chemical gradients can generate pattern formation in biological systems.

180 fluids, the growth of bubbles in foams, and pattern formation in biomembranes.

181 edgehog signal transduction during embryonic pattern formation in both vertebrates and invertebrates.

182 anding the mechanisms underlying distributed pattern formation in brain networks and its content driv

183 rvation has major implications for models of pattern formation in branching trees, and may also be im

184 Various mechanisms govern pattern formation in chemical and biological reaction sy

185 n combination, this leads to the notion that pattern formation in classes of arenethiol molecules is

186 mental platform for the study and control of pattern formation in complex biological excitable system

187 Spontaneous pattern formation in cortical activity may have conseque

188 Some aspects of pattern formation in developing embryos can be described

189 Pattern formation in developing organisms can be regulat

190 gene expression and function underlie neural pattern formation in Drosophila, Tribolium, and potentia

191 our approach using a dataset from studies of pattern formation in Drosophila.

192 sents an alternative class of self-organized pattern formation in ecology.

193 We demonstrate our ability to guide pattern formation in films thick enough to be of interes

194 Photoactivated pattern formation in functional polymers has attracted m

195 f the visual cortex to examine its effect on pattern formation in general and the generation of tempo

196 trains are widely known to control nanoscale pattern formation in heteroepitaxy, but such effects hav

197 s suggests that self-organized hallucinatory pattern formation in human vision is governed by the sam

198 e-scale nonequilibrium self-organization and pattern formation in life is a major challenge, with imp

199 Hedgehog signaling controls pattern formation in many vertebrate tissues.

200 s of mussels (Mytilus edulis) during spatial pattern formation in mussel beds can be regarded as bein

201 orts the tantalizing possibility that Turing pattern formation in natural multicellular systems can a

202 Self-organization and pattern formation in network-organized systems emerges f

203 d oligodendrocyte development but not normal pattern formation in Olig2(-/-) embryos.

204 mediated signalling is required for segment pattern formation in other arthropods, suggest that the

205 cise regulation of caudal, and that anterior pattern formation in particular depends on two localized

206 ata provides a convenient model for studying pattern formation in plant tissues.

207 tal system to study cell differentiation and pattern formation in plants and animals.

208 ning phosphatidylinositol levels and affects pattern formation in plants likely through regulation of

209 ciated aspect of developmental robustness is pattern formation in proportion to size.

210 s well as, more generally, for understanding pattern formation in reaction-diffusion systems.

211 First, pattern formation in resist materials is described and t

212 animals, the principles of morphogenesis and pattern formation in single cells remain largely unknown

213 ment, synchronized oscillatory reactions and pattern formation in space, as manifestation of collecti

214 ergence of the diverse mechanisms underlying pattern formation in specific biological contexts probab

215 estingly suggests some commonalities between pattern formation in the biological and physical systems

216 th requirements imposed by current models of pattern formation in the developing body axis.

217 in various cellular contexts, including axis-pattern formation in the developing egg chamber of Droso

218 Pattern formation in the developing embryo relies on key

219 th requirements imposed by current models of pattern formation in the developing limb.

220 d how canonical Wnt signaling contributes to pattern formation in the developing spinal cord.

221 Motivated by studies of pattern formation in the early Drosophila embryo, we ana

222 A computational model of cellular pattern formation in the growing zebrafish retina was de

223 These observations show that pattern formation in the mouse can occur independent of

224 ell death would not appear to explain failed pattern formation in the mutant PrV.

225 ll death is not a sufficient cause of failed pattern formation in the PrV of the DRG11(-/-).

226 erstanding of molecular events that underlie pattern formation in the retina, we evaluated the expres

227 Cellular pattern formation in the root epidermis of Arabidopsis o

228 transcription factor DRG11 is necessary for pattern formation in the trigeminal nucleus principalis

229 genetic and cellular bases for adult pigment pattern formation in the zebrafish Danio rerio, as well

230 Mutations that affect pattern formation in the zebrafish have been widely stud

231 organized, and a quantitative comparison of pattern formation in them has not been made.

232 ing of the basic elements needed for spindle pattern formation in this pathway.

233 been a very influential system for studying pattern formation in vertebrates.

234 sses, is perhaps most evident in examples of pattern formation in which the different cell types aris

235 Pigment pattern formation in zebrafish presents a tractable mode

236 rting modes of collective ATP-driven dynamic pattern formation including not only the previously desc

237 adult central nervous system and at sites of pattern formation, including the developing limb.

238 hat polarized light has a striking effect on pattern formation indicated by enhanced phase separation

239 m, we present a simplified model to describe pattern formation induced by force-generating bodies emb

240 Zigzag pattern formation is a common and important phenomenon i

241 The resulting pattern formation is a direct consequence of the relativ

242 Pattern formation is a hallmark of coordinated cell beha

243 Our results indicate that proper pattern formation is achieved through transcriptional re

244 Together, this leads to the view that pattern formation is an emergent behavior that results f

245 In cuprates, the pattern formation is associated with the pseudogap phase

246 Coordination of cell division and pattern formation is central to tissue and organ develop

247 In both tissues, pattern formation is dependent on molecular gradients th

248 Pattern formation is governed by the interplay of short-

249 One example of pattern formation is that of irregular eutectic solidifi

250 The spontaneous emergence of pattern formation is ubiquitous in nature, often arising

251 ole of Hedgehog (Hh) signalling in embryonic pattern formation is well established, its functions in

252 proliferation, cell signaling mechanisms and pattern formation, little is known about these same proc

253 reviews recent progress in understanding the pattern formation, maternal effects and evolution of thi

254 of additional regulatory links in a complex pattern formation mechanism.

255 Thus, the considered pattern-formation mechanism is very robust, and similar

256 Systematic validation of pattern formation mechanisms revealed by molecular studi

257 tions as a master controller of development, pattern formation, morphogenesis, and tropic responses.

258 The row and pattern formation of (methylated) anthracenethiols indic

259 tically and experimentally-in the problem of pattern formation of a moving boundary, such as a solidi

260 at the subcellular architecture and cellular pattern formation of a tissue may be regulated by neighb

261 Brain oscillations reflect pattern formation of cell assemblies' activity, which is

262 hat it shows a non-stereotypic cell division pattern, formation of dorsal-ventral polarity, and endog

263 d cells, yet it also causes abnormal budding patterns, formation of enlarged and elongated cells, inc

264 Here we demonstrate that photoactivated pattern formation on azobenzene-containing polymer films

265 ultra-smoothening, self-organized nanoscale pattern formation or degradation of the structural integ

266 bout the actual mechanisms underlying colour pattern formation or evolution.

267 The molecular mechanisms underlying pattern formation, particularly the regulation of format

268 s: a half-centre rhythm generator (RG) and a pattern formation (PF) network, with reciprocal inhibito

269 parate half-centre rhythm generator (RG) and pattern formation (PF) networks has been developed from

270 f the path compared to the timescales of the pattern formation process itself.

271 Here, we investigate the response of this pattern formation process to genetic variation and evolu

272 s in the heart can be formed via a dynamical pattern formation process which does not require tissue

273 t governs the VPC primary-secondary-tertiary pattern formation process.

274 ms currently believed to be important to the pattern-formation process.

275 The hedgehog signaling network regulates pattern formation, proliferation, cell fate and stem/pro

276 The pattern formation required fast GABAergic transmission,

277 This reveals that auxin pattern formation requires coordination between influx a

278 chemical reactions and diffusion to control pattern formation requires the careful design of reactio

279 nto the mechanisms that can give rise to the pattern formation seen in other biological systems such

280 modes of activity on networks and localised pattern formation seen throughout science, such as solit

281 sms with those that specify other aspects of pattern formation, such as spatial and sexual informatio

282 ly considered as components of intracellular pattern formation systems.

283 nally, the model demonstrates that with time pattern formation takes place in the ring, worsening the

284 network architecture that can accomplish the pattern formation task at hand--the formation of three l

285 We identify a process of global pattern formation that causes regions to differentiate b

286 and the autonomous hallucinatory geometrical pattern formation that occurs for unstructured visual st

287 A computational model of cellular pattern formation that used a signaling mechanism arisin

288 are also effective in driving hallucinatory pattern formation (the latter is consistent with predict

289 In strains lacking the -271 tsp of hetR, pattern formation, the timing of commitment to different

290 Pattern-formation theory predicts that such highly order

291 pporting a central universality principle of pattern-formation theory.

292 the mechanism governing the transition from pattern formation to flatness using only parameter-free

293 The dynamics that drive pattern formation usually involve genetic nonlinear inte

294 the study of evolution, development of axis pattern formation, venom production, haplo-diploid sex d

295 The herringbone pattern formation via intercluster interactions is also

296 at Hrp38 poly(ADP-ribosyl)ation controls eye pattern formation via regulation of DE-cadherin expressi

297 To investigate the evolution of neural pattern formation, we identified and determined the expr

298 is of transcriptional regulation in dendrite pattern formation, we used RNA interference (RNAi) to sc

299 ent advances in the statistical mechanics of pattern formation, which suggest that the hallucinatory

300 ting the insights gained into ligand-induced pattern formation within self-assemblies.