ライフサイエンスコーパス: spatial control

1 escence and guide cell adhesion with precise spatial control.

2 enables good tissue penetration and precise spatial control.

3 via an avidin adaptor with a high degree of spatial control.

4 onlinear optical processes with spectral and spatial control.

5 ls for apoptosis induction with temporal and spatial control.

6 lored surfaces that can deliver signals with spatial control.

7 gene expression with exquisite temporal and spatial control.

8 can be introduced under precise temporal and spatial control.

9 fficient, however, and often lack sufficient spatial control.

10 of meiotic onset is under tight temporal and spatial control.

11 n instead promote reactivity through precise spatial control.

12 Our bioorthogonal approach also enables spatial control.

13 er-cell killing mechanisms with temporal and spatial control.

14 guided single cell transplantation with high spatial control.

15 a particular position with a high degree of spatial control.

16 omatic cell types examined with temporal and spatial control.

17 expanded their potential by enabling precise spatial control across nano- to macroscales, supporting

18 By leveraging the spatial control afforded by nanostructured polymer brush

19 ated into mesoporous thin films with precise spatial control along the nanoscale layer thickness.

20 for example transient laser heating, adding spatial control and great flexibility to the processing.

21 etect and kill biofilm bacteria with precise spatial control and in a short timeframe.

22 h understanding of the biosynthesis pathway, spatial control and regulation mechanism of patulin in f

23 fined active matter in contexts ranging from spatial control and sorting of microorganisms to the des

24 By using light as the logic inputs, both spatial control and temporal control were achieved.

25 c maturation of animal oocytes demands tight spatial control and temporal precision.

26 ion method reported here allows temporal and spatial control and will prove to be a useful tool in st

27 tors, and p-n junctions with precise sub-mum spatial control, and a rectification ratio of over 10(4)

28 vity of the associations to model selection, spatial control, and latency period as well as estimatin

29 such as signaling specificity, mechanisms of spatial control, and noise suppression.

30 and IAP cells; is subjected to temporal and spatial control; and depends in part on BRAF signalling

31 fied to present synNotch ligands with coarse spatial control, applications in tissue engineering gene

32 genetic modifications under temporal and/or spatial control are invaluable to functional genomics an

33 ts lacking motility traits surrender to host spatial control, becoming aggregated and entrapped withi

34 tion of the Smo-Evc2 complex is under strict spatial control, being restricted to a distinct ciliary

35 many cases, it is unclear how escaping host spatial control benefits gut bacteria and how changes in

36 reate complex nanostructures with impressive spatial control but struggle to fabricate gaps on the or

37 eptor (MOR) expression is under temporal and spatial controls, but expression levels of the MOR gene

38 Here, we achieve spatial control by biopanning a phage library to discove

39 Our design incorporates temporal and spatial control by the use of chemical and optogenetic m

40 mbined with two-photon excitation, excellent spatial control can be achieved even in complex and high

41 Through intracellular spatial control, cells are able to organize and regulate

42 otion processing and the processing of a non-spatial control complex auditory property (timbre) than

43 e cell phenotypes in vivo, with temporal and spatial control, could have significant impact on a wide

44 a strong initial bottleneck, beginning with spatial control, demographic manipulation via biased mal

45 However, difficulties with precise spatial control during their assembly currently impede a

46 te provides uniform nanostructures with good spatial control, effective encapsulation of dye molecule

47 tes at which two different negatively acting spatial control factors bind, the functions of which are

48 Furthermore, both the negative spatial control functions and response to LiC1 require t

49 ate designer DNA architectures with accurate spatial control has allowed researchers to explore novel

50 In the x-ray region, however, spatial control has been virtually static mainly due to

51 Significantly, the spatial control in both deposition and extraction steps

52 These studies underscore the relevance of spatial control in chromatin-associated protein ubiquiti

53 ity may be a general mechanism for achieving spatial control in diverse biological processes.

54 form for disentangling the role of space and spatial control in multiple cellular contexts and a basi

55 ellular contexts and a basis for engineering spatial control in signaling cascades through localizati

56 les light-induced, chemical crosslinking for spatial control in the gel state.

57 by Ca(2+) and Mg(2+) together with a strong spatial control in the local fiber orientation.

58 lar ferroelectric metamaterials with precise spatial control in virtually any three-dimensional (3D)

59 o direct migration with precise temporal and spatial control in vivo.

60 To incorporate this concept of spatial control into more practical battery electrodes,

61 ed to correlate, with exquisite temporal and spatial control, intracellular biochemical action with g

62 However, NPC spatial control is important, as a dbp5-R256D/R259D nup4

63 In Drosophila, spatial control is primarily provided by the GAL4/UAS sy

64 o distribute and confine capture probes with spatial control, making it possible to achieve a uniform

65 composition utilizing multimaterial actinic spatial control (MASC) during additive manufacturing.

66 Cbl plays a crucial role in the temporal and spatial control of 5-HT(2A)R recycling.

67 proteins, a protein family implicated in the spatial control of actin assembly and previously shown t

68 ed a micropatterning method that enables the spatial control of actin assembly.

69 These novel roles for palmitoylation in the spatial control of actin dynamics and kinase signaling p

70 eveals a novel mechanism for domain-specific spatial control of actin-based motility in the growth co

71 cellular trafficking network linked to tight spatial control of active Src and FAK levels, and so cru

72 Spatial control of active Src requires the trafficking p

73 4-PI3Kalpha assembly defines a mechanism for spatial control of agonist-stimulated PI3K-Akt signallin

74 efficient alpha4-mediated migration requires spatial control of alpha4 phosphorylation by protein kin

75 rease the stability and reach a temporal and spatial control of angiotensin-(1-9) release.

76 This spatial control of AP backpropagation was mediated by Ia

77 ctivity in a det3 background showed that the spatial control of AtMYB61 expression was lost.

78 Here, we investigate the spatial control of autophagic proteasome turnover in bud

79 Spatial control of auxin application is reduced, but thi

80 The temporal and spatial control of auxin distribution has a key role in

81 of the nervous system requires temporal and spatial control of axon guidance signaling.

82 This spatial control of bacterial gene expression could be us

83 protein modules enable precise temporal and spatial control of biological processes in non-invasive

84 We propose that the spatial control of BM production along two tissue axes p

85 nvolved in local Ca(2+) signaling and in the spatial control of Ca(2+) extrusion, but how different P

86 teracting with the bud neck is maintained by spatial control of catastrophe and rescue, which extends

87 Depletion of SH3BP1 resulted in loss of spatial control of Cdc42 activity, stalled membrane remo

88 al knock-out systems that allow temporal and spatial control of Cdk5 expression in the adult brain.

89 Proper spatial control of cell cycle timing can mitigate these

90 d to identify the signal responsible for the spatial control of cell death.

91 ir innervation requires precise temporal and spatial control of cell differentiation.

92 ze leaf shape does not depend on the precise spatial control of cell division, and support the genera

93 o be of critical importance for temporal and spatial control of cell expansion.

94 We have studied the temporal and spatial control of cell migration from the external germ

95 omplex process dependent on precise temporal-spatial control of cell proliferation, differentiation a

96 of aleurone mutant phenotypes, temporal and spatial control of cell type-specific fluorescent marker

97 development require the precise temporal and spatial control of cell-shape changes.

98 eceptors (GPCRs) is crucial for temporal and spatial control of cell-surface GPCR signaling.

99 tures guide cell adhesion, providing precise spatial control of cells without requiring adhesive liga

100 adigm for the role of peptide signals in the spatial control of cellular differentiation.

101 Our data indicate tight spatial control of chromatin motions after genomic insul

102 We propose that spatial control of ciliogenesis uncouples or specifies s

103 ation of active myosin, thereby ensuring the spatial control of concerted contraction during cytokine

104 Our results demonstrate spatial control of condensation as a new tool for constr

105 development is unclear because experimental spatial control of cortical cell arrangement is technica

106 roscale and the microscale, enabling precise spatial control of crosslink density that results in hig

107 termed ZMMs, are required for formation and spatial control of crossovers throughout eukaryotes.

108 Spatial control of cytokinesis in plant cells depends on

109 ropose that POK1 and POK2 participate in the spatial control of cytokinesis, perhaps via an interacti

110 tric division of fission yeast cells through spatial control of cytokinesis.

111 on of source/drain contact asymmetry enables spatial control of de/doping and creation of single-mate

112 of otoconia requires a complex temporal and spatial control of developmental and biochemical events.

113 ction motifs imparting distinct temporal and spatial control of DGK activity to each isozyme.

114 A new model for the spatial control of division planes by the Min system in

115 y complex organizational principles, such as spatial control of division site placement by intracellu

116 odules independently govern the temporal and spatial control of DNA replication in the asymmetrically

117 ng that the immortalization process modifies spatial control of DNA replication.

118 through this manner, it limits temporal and spatial control of DNA-based logic operations.

119 Using microcontact printing to achieve spatial control of DNA-surface patterning and DNA-functi

120 The integrity of the barrier depends on spatial control of dynamics of actin cytoskeleton in the

121 n of ciliary and flagellar motility requires spatial control of dynein-driven microtubule sliding.

122 n metal dichalcogenides enable unprecedented spatial control of electron wavefunctions, leading to em

123 d an internal cis-regulatory switch by which spatial control of endo16 expression is shifted from Mod

124 ogenesis depends on the precise temporal and spatial control of epithelial dynamics.

125 All life demands the temporal and spatial control of essential biological functions.

126 form chromatin is essential for temporal and spatial control of eukaryotic genomes.

127 veals the mechanistic basis for temporal and spatial control of FANCD2:FANCI monoubiquitination that

128 mplex tissues in eukaryotes requires precise spatial control of fate-specifying genes.

129 e that an HD-ZIP protein plays a role in the spatial control of fiber differentiation.

130 Finally, spatial control of flagella in B. subtilis seems more re

131 se results raise the possibility that proper spatial control of FrzS has an important role in the reg

132 nent localisation, dynamic localisation, and spatial control of functional materials within MOF cryst

133 with uniform and controllable dimensions and spatial control of functionality.

134 The spatial control of GEN1 therefore contributes to genome

135 imate link between lncRNA expression and the spatial control of gene expression during development.

136 orphogenesis requires intricate temporal and spatial control of gene expression that is executed thro

137 Spatial control of gene expression, at the level of both

138 Caulobacter cell cycle requires temporal and spatial control of gene expression, culminating in an as

139 nd developmental processes by regulating the spatial control of gene expression.

140 ntrols together provide precise temporal and spatial control of gene expression.

141 this positioning contributes to temporal and spatial control of gene expression.

142 or AKAP12 and sheds light into mechanisms of spatial control of gene expression.

143 tal transitions require precise temporal and spatial control of gene expression.

144 ronmental cues requires precise temporal and spatial control of gene expression.

145 ns of this adaptable and swift mechanism for spatial control of gene function.

146 itfalls, in principle, enabling temporal and spatial control of gene recombination.

147 trafficking is pivotal for the temporal and spatial control of GPCR signaling and is regulated by mu

148 FLAIR revealed precise spatial control of growth factor-induced Rac activation,

149 of outer-membrane protein patterning in the spatial control of intracellular processes, adding an im

150 gels may also provide enhanced temporal and spatial control of intratumoral conformal drug delivery.

151 liquid-liquid phase separation to study the spatial control of irreversible protein aggregation in t

152 diverse cellular processes depends on tight spatial control of its activity.

153 otic flagellum requires precise temporal and spatial control of its constituent dynein motors.

154 rgistically promote centromere alignment via spatial control of kinetochore-microtubule dynamics.

155 These results suggest that temporal and spatial control of ligand availability conferred by D2 p

156 remains challenging, in particular when fine spatial control of light is required to achieve local sp

157 tudy the molecular mechanisms underlying the spatial control of lignification.

158 Altogether, we propose that the spatial control of lignin chemistry depends on different

159 We have established an approach for the spatial control of lipid phase separation in tethered po

160 In conclusion, Asp(69) is crucial for the spatial control of loop A, the particular molecular conf

161 erstanding of the mechanisms underlying this spatial control of lrgAB expression, we carried out a de

162 owever, in plants, little is known about the spatial control of MAPK signaling.

163 Precise spatial control of materials is the key capability of en

164 Through spatial control of metal ion content, we created a conti

165 oenzyme, providing a mechanism for exquisite spatial control of metalloenzyme activity.

166 ia (SSM) pool density, implicating it in the spatial control of mitochondrial localization.

167 or phosphatases involved in the temporal and spatial control of moesin, we identify PP1-87B RNAi as h

168 science that have often required programmed spatial control of molecules and atoms in three-dimensio

169 Spatial control of mRNA translation can generate cellula

170 Here we demonstrate a technique that allows spatial control of multiple cell types at single cell le

171 CtrA activity required for the temporal and spatial control of multiple cell-cycle events.

172 urface chemistry of colloidal nanoparticles, spatial control of nanoparticle surface chemistry remain

173 We show that both components to spatial control of nanos translation initiate during oog

174 The temporal and spatial control of organ-specific endoderm progenitor de

175 protein MEX-3 is central to the temporal and spatial control of PAL-1 expression in the C. elegans ea

176 Creating this polymer network allows for the spatial control of pendant reactive sites and dramatical

177 To understand the temporal and spatial control of PI4P generation across the Golgi comp

178 n this chapter, we discuss the mechanics and spatial control of polarity development and cytokinesis,

179 The power of such temporal and spatial control of polymerization can be found in nature

180 likely to be essential for the temporal and spatial control of protein associations at the membrane-

181 ns provide cells with exquisite temporal and spatial control of protein function.

182 binding protein (CPEB) provides temporal and spatial control of protein synthesis required for early

183 Spatial control of proteolysis is emerging as a common f

184 y regulator of lens vesicle polarity through spatial control of Prox1, Jag1, p27(Kip1) (Cdkn1b) and p

185 This mechanism is critical for spatial control of Ran-guanosine triphosphate (GTP) grad

186 Our work establishes a novel spatial control of Recombination-Dependent Replication (

187 interactions providing precise temporal and spatial control of regulatory gene expression.

188 Porphyrin-phospholipid liposomes demonstrate spatial control of release of entrapped gentamicin and t

189 ole for alternative membrane interactions in spatial control of RGS-PX proteins in cell signaling and

190 The temporal and spatial control of Rho GTPase signaling pathways is a ce

191 Spatial control of RhoGTPase-inactivating GAP components

192 hanism for S1P and provide insights into how spatial control of S1P activity underpins cholesterol ho

193 However, the temporal and spatial control of SET8 activity remains elusive.

194 uction of biological noise, and temporal and spatial control of signal transduction.

195 ulphides in a matrix with high surface area, spatial control of solid-state sulphur and lithium sulph

196 ed a c-Src-GFP fusion protein to address the spatial control of Src activation and the nature of Src-

197 lus vulgaris ABI3-like factor (PvALF) in the spatial control of storage protein gene expression is we

198 ed self-assembly for molecular machines, the spatial control of supramolecular polymerization with sy

199 e site of irradiation, thus allowing for the spatial control of surface derivatization.

200 e LH2 complex is readily patterned simply by spatial control of surface polarity.

201 ds represent a general tool for temporal and spatial control of T cell signaling and extend the reach

202 st time the importance of nuclear export and spatial control of telomeric proteins in telomere mainte

203 f the natural sciences, but it requires high spatial control of the 3D structure of matter.

204 also requires a method for an efficient and spatial control of the cAMP pool in the pathogen or in t

205 supramolecular arrays provide a route to the spatial control of the chemical functionality of a surfa

206 u(I), or added as a Cu(I) salt, temporal and spatial control of the CuAAC reaction is not readily ach

207 scaffold; and demonstration of temporal and spatial control of the distribution of non-reactive solu

208 Temporal and spatial control of the doping is achieved by varying the

209 ion thereby providing extensive temporal and spatial control of the experimental parameters of gene e

210 the site of irradiation, thus, allowing for spatial control of the ligation or labeling.

211 his challenge as they allow for atomic-level spatial control of the molecular subunits that comprise

212 so that a photomask is not required for the spatial control of the plug location.

213 Spatial control of the protease cascade relies on the Pi

214 This would facilitate spatial control of the remodelling of mRNP protein compo

215 e site of irradiation, thus allowing for the spatial control of the surface derivatization.

216 has an appropriate T(m), as well as accurate spatial control of the temperature in the microfluidic d

217 e-integrated microheaters to achieve precise spatial control of the temperature profile (i.e., hotspo

218 Temporal and spatial control of these signaling cascades is achieved

219 sms have been suggested for the temporal and spatial control of these transformations.

220 d Hedgehog signaling underlying temporal and spatial control of tissue growth and specification in de

221 uron growth cones and that both temporal and spatial control of Toll expression is crucial for its ro

222 e function is necessary for the temporal and spatial control of tracheal repopulation.

223 Precise temporal and spatial control of transcription is a fundamental compon

224 anscriptional activator from yeast to obtain spatial control of transgene expression in all organs of

225 Cell-specific promoters allow only spatial control of transgene expression in Caenorhabditi

226 , QS and quinic acid to achieve temporal and spatial control of transgene expression in various tissu

227 expression systems allow tight temporal and spatial control of transgene expression, invaluable in s

228 ical systems but also allow for temporal and spatial control of transition-metal catalysis through ge

229 n but could provide a means for temporal and spatial control of translation.

230 ion, our results suggest a mechanism for the spatial control of tubulin modifications that is require

231 The data suggest new CRM1 functions in spatial control of vesicle coat-assembly, centrosomes, a

232 interference (RNAi) enables temporal and/or spatial control of virtually any gene, making it useful

233 This system could allow for spatial control of Wg signaling to targets at different

234 sed by E. coli and other bacteria to achieve spatial control of Z-ring assembly.

235 Temporal and spatial controls of cell migration are crucial during no

236 However, despite the temporal and spatial control offered by LFS, such a procedure lacks c

237 We sought to exert precise spatial control over activation of TGF-beta signaling.

238 cally patterned surface chemistry to provide spatial control over adhesion sites, and elastic deforma

239 ction of functional synthetic cells requires spatial control over arrays of biomolecules within the c

240 sequential events provide both temporal and spatial control over beta-actin mRNA translation, which

241 bound compartments, affording sequential and spatial control over biochemical reactions.

242 developing alternatives capable of achieving spatial control over bone formation.

243 n of cell-adhesive ligands and BMP-2 allowed spatial control over cell adhesion and osteogenic differ

244 Precise spatial control over cell spreading and orientation has

245 ndritic spine and synapse plasticity through spatial control over cofilin activation.

246 constitutively; thus, they provide intrinsic spatial control over DNA targeting activities but natura

247 /(Eu(0.7)Sr(0.3)MnO(3))n] x m, as a route to spatial control over electronic bandwidth and ferromagne

248 for the normal eye to maintain very specific spatial control over FGF expression in order to prevent

249 t scaffolding provided by DNA structure with spatial control over fluorophore positioning allows the

250 in combining the attributes of temporal and spatial control over gene expression into a single syste

251 constitutively active, precise temporal and spatial control over genome editing and transcriptional

252 lly flexible micropatterning method provides spatial control over growth of IC-21 murine peritoneal m

253 ctive in guiding Li deposition and realizing spatial control over Li nucleation.

254 res is reported, which allows high-levels of spatial control over mechanical and chemical properties.

255 Spatial control over molecular movement is typically lim

256 We conclude that precise spatial control over MT nucleation is achieved by coupli

257 Spatial control over MyoII exchange kinetics establishes

258 polarized growth with enhanced temporal and spatial control over prolonged periods.

259 ese systems offer unprecedented temporal and spatial control over protein function.

260 Realizing atomic-level spatial control over qubits, the fundamental units of bo

261 sed the GAL4-UAS and FLP-FRT systems to gain spatial control over reporter gene expression.

262 Together, our findings suggest that host spatial control over resident microbiota plays a broader

263 izes to a set of cortical nodes that provide spatial control over signaling for entry into mitosis.

264 Precise spatial control over the electrical properties of thin f

265 shapes likely reflects precise temporal and spatial control over the formation of polarity axes.

266 ue, mostly involving the lack of temporal or spatial control over the genetic 'lesion'.

267 We display spatial control over the immobilization of a variety of

268 Gaining spatial control over the nanoparticle incorporation is u

269 on of the material and facilitating enhanced spatial control over the polymerization.

270 We demonstrate that spatial control over the positioning of fluorophores on

271 lution, possibly to allow tight temporal and spatial control over the production of this key signalin

272 This was done to gain spatial control over the reaction.

273 disassembly kinetics, enabling temporal and spatial control over the release of multiple components

274 Spatial control over the trapped molecules is achieved b

275 e-crystal microwaveguides in order to attain spatial control over their light output.

276 increase the range of cell types and deliver spatial control over their location.

277 rganic optical waveguides in order to attain spatial control over their output in two and three dimen

278 e waveguides requires downsizing and precise spatial control over their shape and size at the microsc

279 volving topological insulators (TIs) require spatial control over time-reversal symmetry and chemical

280 system, which provides the experimenter with spatial control over transgene expression.

281 To permit temporal as well as spatial control over UAS-transgene expression, we have e

282 Spatial control over Z ring assembly is achieved by two

283 nce of repressive regulatory interactions in spatial control processes.

284 up of the division site, cytokinesis and its spatial control remain an open-ended field with outstand

285 ly synthesized in bulk solution, lacking the spatial control required for on-chip integration.

286 Our data elucidate the temporal and spatial control surrounding a constitutive, potentially

287 o affect performance in a difficulty-matched spatial-control task that did not require processing of

288 ogether with non-spatial auditory and visual spatial control tasks.

289 In addition to spatial control, temporal control is easily attainable v

290 eversibility, dynamic induction strength and spatial control, that are difficult to obtain with chemi

291 Cellular functions are regulated with high spatial control through the local activation of chemical

292 lls (NSCs) to divide with tight temporal and spatial control to produce different daughter cell types

293 yt-IV-regulated BDNF secretion is subject to spatial control to regulate synaptic function in a site-

294 FETCH enables precise temporal and spatial control to visualize tagged proteins in vivo, fe

295 for new nanotechnological devices for which spatial control translates into a higher level of sophis

296 The tight temporal and spatial control underlying this process of somitogenesis

297 alian cells, either globally or with precise spatial control using a steerable laser.

298 ave been achieved using small molecules, and spatial control using light, no singular system with con

299 n of inter-leg timing, whereas adaptation of spatial control was intact.

300 The spatial control within the final architecture allows the