ライフサイエンスコーパス: spatial control

1 ls for apoptosis induction with temporal and spatial control.

2 lored surfaces that can deliver signals with spatial control.

3 guided single cell transplantation with high spatial control.

4 gene expression with exquisite temporal and spatial control.

5 can be introduced under precise temporal and spatial control.

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

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

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

9 omatic cell types examined with temporal and spatial control.

10 escence and guide cell adhesion with precise spatial control.

11 enables good tissue penetration and precise spatial control.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 Spatial control of active Src requires the trafficking p

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

51 This spatial control of AP backpropagation was mediated by Ia

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

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

54 Spatial control of auxin application is reduced, but thi

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

56 This spatial control of bacterial gene expression could be us

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

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

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

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

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

62 Proper spatial control of cell cycle timing can mitigate these

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

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

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

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

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

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

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

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

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

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

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

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

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

76 Spatial control of cytokinesis in plant cells depends on

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 The spatial control of GEN1 therefore contributes to genome

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 Spatial control of mRNA translation can generate cellula

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

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

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

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

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

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

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

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

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

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

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

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

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

136 Spatial control of proteolysis is emerging as a common f

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

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

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

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

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

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

143 Spatial control of RhoGTPase-inactivating GAP components

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 Spatial control of the protease cascade relies on the Pi

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

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

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

164 Temporal and spatial control of these signaling cascades is achieved

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

186 Precise spatial control over cell spreading and orientation has

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

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

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

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

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

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

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

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

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

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

197 Spatial control over MyoII exchange kinetics establishes

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

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

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

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

202 Precise spatial control over the electrical properties of thin f

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

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

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

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

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

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

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

210 Spatial control over the trapped molecules is achieved b

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

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

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

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

215 Spatial control over Z ring assembly is achieved by two

216 nce of repressive regulatory interactions in spatial control processes.

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

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

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

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

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

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

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

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

225 The spatial control within the final architecture allows the