ライフサイエンスコーパス: architectural

1 r results find applications in areas such as architectural acoustics, indoor localization, virtual re

2 y region and by muscle sheet, IMAs displayed architectural adaptations to the different loci.

3 the oscillatory changes were related to the architectural alterations in cortical cytoskeleton, the

4 platform, PANorama, which measures multiple architectural and branching phenotypes from images simul

5 n, organization, and compliance provide both architectural and chemical cues that modulate tissue str

6 and silicon) that are characterized by high architectural and chemical robustness.

7 Control over the architectural and electronic properties of heterogeneous

8 ergy harvesting devices and because of their architectural and functional flexibility, can potentiall

9 etic information that gives rise to a cell's architectural and functional machinery.

10 the bone marrow, a tissue with higher-order architectural and functional organization than previousl

11 ctive processing framework lacks many of the architectural and implementational details needed to ful

12 ficiency of different nutrients induces root architectural and morphological changes that are, at lea

13 The El Palenque palace exhibits certain architectural and organizational features similar to the

14 These architectural and regulatory principles appear conserved

15 For ASG2, we demonstrate its remarkable architectural and sequence similarities to spider silk f

16 te the human system due to immunophenotypic, architectural, and functional inter-species variability.

17 Although the architectural arrangement of parts of the Y complex has

18 R5 and RbBP5, suggesting a restraint for the architectural arrangement of subunits within the complex

19 changes, dysplastic nevi with structural and architectural atypia, and melanoma.

20 share similar transcription factor-mediated architectural "blueprints."

21 Defective architectural cell function explains the immunodeficienc

22 This architectural change facilitates cognate promoter-enhanc

23 d biochemical mechanisms that underlie these architectural changes and highlight their particular rel

24 icient for functional cohesin exhibit global architectural changes associated with loss of cohesin/CT

25 intramolecular coevolution with only modest architectural changes in lectin and esterase domains; an

26 lts from a key proline residue that produces architectural changes in the channel pore alpha-helical

27 hat sulindac sulfide does not induce drastic architectural changes in the fibrillar structure but int

28 The suite of morphological and architectural changes induced by high ambient temperatur

29 xaggerated by chronic stress exposure, where architectural changes lead to persistent loss of PFC fun

30 date, the simultaneous depiction of 3D micro-architectural changes of endplate with aging and interac

31 as been achieved, the presence of underlying architectural changes on biopsies can identify patients

32 tructural and compositional analysis reveals architectural changes that begin with the incorporation

33 transporters and the ability to induce root architectural changes to forage P.

34 ing mitosis the chromatin undergoes dramatic architectural changes with the halting of the transcript

35 plants displayed profound physiological and architectural changes, depending on the tissue, includin

36 ate rhizosphere information into global root architectural changes.

37 sis with CERK1 required for AMF-induced root architectural changes.

38 rom multi-omic networks and validating their architectural characteristics based on innovative comput

39 e SGIC separation mechanism and derive chain architectural characteristics of polymer chains.

40 This social chromosome shares architectural characteristics with that of the fire ant

41 formation and communication systems offering architectural choices that combine photonics with electr

42 nization is in mediating interactions within architectural chromosome compartments, rather than speci

43 present the most important considerations in architectural coating design.

44 in the context of developing new generation architectural coating materials.

45 In this review, we discuss the architectural commonality between immunity and metabolis

46 Through expanded architectural comparisons between these complexes and HI

47 including both the chemical composition and architectural complexity - of biointerfaces.

48 However, the architectural complexity and heterogeneous contents asso

49 living materials is challenging due to their architectural complexity and spatiotemporal heterogeneit

50 ulpture of wing scales vary widely, and this architectural complexity arises from variations in the d

51 Cellular diversity and architectural complexity create barriers to understandin

52 While we have come to appreciate the architectural complexity of microbially synthesized seco

53 reate 4D nanostructures with the chemical or architectural complexity of their biological counterpart

54 llular networks of arbitrary biophysical and architectural complexity using the logic of NEURON and a

55 tions were able to delay the general loss of architectural complexity, as the benefits of grazing in

56 s of live coral cover resulting in a loss of architectural complexity.

57 ulty of structure determination due to their architectural complexity.

58 olyse the polysaccharide chitin, an abundant architectural component in invertebrates and fungi.

59 NEAT1 is an essential architectural component of paraspeckle nuclear bodies, w

60 sed on their link to signaling molecules and architectural components important in disease pathogenes

61 Me(2+) ions are intimate architectural components of each active site, where they

62 The sensor consists of only simple architectural components, and as such they are inexpensi

63 genes, but referring to the phenotype), and architectural concepts including morphology, geometry, a

64 mon network functions may reveal active-site architectural connections that are critical for function

65 Here we demonstrate that this strong architectural constraint is not required for effective e

66 Their positioning in the architectural context of imposed specific interactions f

67 Architectural control over these cross-beta assemblies,

68 Metallomacromolecular architectural conversion is expanded by the characteriza

69 iled substitution patterns, highlight common architectural cores, and discuss unusual or rare structu

70 explanation for how the stromal ECM encodes architectural cues for branch orientation as well as how

71 gative impacts, from the construction of the architectural cytoskeleton of cells to the formation of

72 Architectural defects arise because loss of Rac1 disrupt

73 diagrams that take into account this updated architectural design are presented.

74 etabolic rate and body mass are based on the architectural design of the cardiovascular system and pr

75 r, our data provide a first glimpse into the architectural design of the CTP complex and reveals uniq

76 Despite the substantial impact of architectural design on people's visual experience of bu

77 rural diaphragm is generated by a unique myo-architectural design, each of which forms a "noose" arou

78 Modifiable factors include build age, architectural design, level of maintenance, variations i

79 on, chain-end functional groups, and polymer architectural design.

80 actors are essentially determined by the ICU architectural design.

81 work and we propose an initial model for its architectural design.

82 Here, we present the external architectural details of BK channels using lanthanide-ba

83 addition, there is no evidence that protein architectural differences are driven by lineage-specific

84 ructure of ceCblC provides insights into how architectural differences at the alpha- and beta-faces o

85 The reconstruction method captures unique architectural differences between lines, such as leaf an

86 Analysis of this line revealed architectural differences in myofibrils of the distinct

87 ibility of the low-pH-induced transition and architectural differences in the fusion proteins themsel

88 wn color (ICC, 0.40; 95% CI, 0.35-0.44), and architectural disorder (ICC, 0.43; 95% CI, 0.39-0.48).

89 ria associated with melanoma included marked architectural disorder (odds ratio [OR], 6.6; 95% CI, 5.

90 r protein composition, there are exceptional architectural dissimilarities between opisthokont (yeast

91 atively and the presence or absence of crypt architectural distortion and eosinophilia was documented

92 DBT, with increased recall examinations for architectural distortion and mass (P < .001) and decreas

93 Architectural distortion was the imaging finding identif

94 The spinal cord showed architectural distortion, severe neuronal loss, and micr

95 For patients with masses and architectural distortion, the difference in recall rates

96 ons, asymmetry or focal asymmetry, mass, and architectural distortion.

97 s 2.5% [237 of 9364], respectively; P = .90; architectural distortion: 2D two-dimensional + 3D three-

98 with which to biopsy DBT-detected suspicious architectural distortions not visualized at mammography

99 The mammographic features (masses, architectural distortions, calcifications, focal asymmet

100 radiographs were obtained, and for masses or architectural distortions, control mammography or DBT wa

101 masses with microcalcifications) and 21 were architectural distortions.

102 ovide a framework for mechanistic studies of architectural diversification.

103 to diversified organisms, during a period of architectural diversification.

104 ate reconstruction we identify two stages of architectural diversification.

105 Architectural diversity appears to matter considerably f

106 root traits that reliably capture heritable architectural diversity as well as environmentally induc

107 res, but the functional significance of this architectural diversity is not yet understood.

108 ity, prodigious chemical, organizational and architectural diversity is revealed.

109 We begin with a brief introduction to the architectural diversity of bimetallic nanocrystals, foll

110 is critical for capsid assembly, both as an architectural element of the CA hexamer and pentamer and

111 modifications associated with regulatory and architectural elements affect patterns of gene expressio

112 f new secondary structures that can serve as architectural elements of innovative materials, molecula

113 cture-guided mutations of conserved tertiary architectural elements of the ligand binding domain usin

114 e filament proteins lamin A and C, two major architectural elements of the mammalian cell nucleus.

115 Chromatin boundaries are architectural elements that determine the three-dimensio

116 This structure reveals architectural elements unique to eukaryotic Cys-loop rec

117 This structure reveals two architectural elements unique to glycyl initiases and cr

118 and facilitates the formation of a favorable architectural environment for ICL repair processing.

119 y of SPBCL as a platform for controlling the architectural evolution of multimetallic nanoparticles i

120 and to discover the forces underpinning the architectural evolution.

121 ified heightened expression of the chromatin architectural factor High Mobility Group AT-hook 1 (HMGA

122 ucture in eukaryotic cells involves abundant architectural factors such as high mobility group B (HMG

123 n or changes in transcription, chromatin, or architectural factors, which are coordinately regulated

124 gh Xist attracts some interactors, it repels architectural factors.

125 Bow-tie or hourglass structure is a common architectural feature found in many biological systems.

126 gal homolog, nhTMEM16, revealed an important architectural feature of this protein family in the form

127 For other art forms (ambient and architectural features and interior design), we did a na

128 53 (Cdh1(d/d)Trp53(d/d)) clearly demonstrate architectural features characteristic of type II ECs, in

129 In summary, we have uncovered key architectural features in the cobalamin-binding pocket t

130 muxFM data, and accurately reproduces known architectural features of cortical synapse distributions

131 e use a model of cascade spreading to reveal architectural features of human brain networks that faci

132 Network analysis was used to define global architectural features of intrinsic cerebral nuclei circ

133 analysis tools supporting the extraction of architectural features of root systems has increased in

134 terpretation for many previously unexplained architectural features of the central complex.

135 To reveal global architectural features of the cortical association conne

136 c, interior design including visual art, and architectural features on health outcomes in surgical pa

137 s nature images and more spacious rooms, and architectural features providing more sunlight had posit

138 utants of Calkro_0111 revealed the essential architectural features required for catalytic function.

139 While it is well-known that architectural features such as flexible junctions betwee

140 These results reveal chromatin architectural features that orient transcription at dive

141 Crystallographic analysis reveals architectural features that promote enhanced biochemical

142 Hierarchically designed structures with architectural features that span across multiple length

143 compressed graphs convey network motifs and architectural features useful for understanding both sma

144 technologies enables the systematic study of architectural features within the antibody conjugated dr

145 ldelta, Pol, and Polzeta, which share common architectural features, such as the exonuclease/polymera

146 to design functional oxides with multiscale architectural features.

147 ent upon its unique cellular composition and architectural features.

148 eptide scaffolds offer chemical versatility, architectural flexibility and structural complexity, but

149 ons to Mesoamerica before the post-A.D. 1040 architectural florescence in Chaco Canyon.

150 electron microscopy (EM) images, defining an architectural foundation at the ciliary base.

151 matin-looping factor that contributes to the architectural foundation of the genome by providing sequ

152 ed Central project, using the PubMed Central architectural framework, workflows and processes.

153 Our analysis suggests that the architectural functionality of TADs arises from the inte

154 erochromatin, co-immunoprecipitated with the architectural heterochromatin proteins HP1, DEK1, and AT

155 Investigation of the architectural (i.e. bulge vs. contiguous pairs) and sequ

156 labels with DNP NMR enables determination of architectural information about polymeric protein system

157 at BRD2, but not BRD4, co-localizes with the architectural/insulator protein CCCTC-binding factor (CT

158 Architectural integrity of the mitotic spindle is requir

159 y rich dynamic behavior without losing their architectural integrity.

160 they will yield the necessary insights into architectural intimacies at the atomic level.

161 f GO oxidation state, allowing control of GO architectural laminate (GOAL) spacing and permeability.

162 chers, and simple suggestions for artificial/architectural lighting are provided for regulatory autho

163 chically partition fold space and define the architectural make up of proteins.

164 Elaborate architectural manipulation of nanohybrids with multi-com

165 This architectural map explains the vast majority of the elec

166 We constructed a computerized architectural map of the branching process throughout fe

167 a self-assembly topology enabling a net-like architectural mimetic of native extracellular matrices c

168 These data allowed us to present an architectural model for ODA16-mediated IFT of ODAs.

169 te, to our knowledge, the most comprehensive architectural model of the human nuclear pore complex to

170 chroism spectroscopy are consistent with our architectural model.

171 road ramifications for enhancer function and architectural models of transcriptional elongation.

172 The results lead to architectural models that explain how integration and ex

173 ted in different and sometimes controversial architectural models.

174 ross a range of magnitudes without requiring architectural modifications.

175 is, D14L is dispensable for AMF-induced root architectural modulation, which conversely relies on CER

176 diac extracellular matrix (ECM) is a complex architectural network consisting of structural and nonst

177 There were no bone architectural or bone mineral density differences by mic

178 ally stable host/guest metal adducts display architectural ordering comparable to that of the enniati

179 ins at A level uncovered general patterns of architectural origin and diversification.

180 s hypothesized to follow the "site I-II-III" architectural paradigm, with site I of p19 being require

181 topological characteristics as well as root architectural parameters are computed.

182 present a novel approach for recovering root architectural parameters based on image-analysis techniq

183 al nanowires with sub-10 nm control over the architectural parameters in both axial and radial dimens

184 The code consists of three independent architectural parameters-network strand length, side-cha

185 led with sandy soil results in a set of root architectural parameters.

186 which determined a particular subset of root architectural parameters.

187 dendritic and/or round cells; a nonspecific architectural pattern at the dermoepidermal junction (DE

188 ly of the gut microbiota follows predictable architectural patterns that correlate with the developme

189 is of the participating cell types and their architectural patterns.

190 ical phene of long, dense root hairs and the architectural phene of shallower basal root growth are s

191 emplate for the generation of supramolecular architectural photopolymerizable materials.

192 Architectural plans for construction of the HOR began in

193 se results suggest an important role of root architectural plasticity across future rice crop conditi

194 In this study, the relationship between root architectural plasticity and adaptability (i.e. yield st

195 oth populations, and one locus for both root architectural plasticity and grain yield was detected.

196 Relationships among root architectural plasticity for root dry weight, root lengt

197 Our findings emphasize the importance of architectural plasticity in response to environmental ch

198 e identified as hot spots with multiple root architectural plasticity traits in both populations, and

199 Root architectural plasticity traits were related to 13 (Aus

200 ions varied in the soil depth effect on root architectural plasticity traits, none of which resulted

201 ience a range of growth conditions, and root architectural plasticity will be an important characteri

202 Trees are capable of tremendous architectural plasticity, allowing them to maximize thei

203 at neuromorphic computing, despite its novel architectural primitives, can implement deep convolution

204 metric unit reported to date and follows the architectural principle for dsRNA viruses that a 120-sub

205 is offers a mechanism to understand a common architectural principle of biological systems, and a way

206 ned experimentally, indicating a fundamental architectural principle of the brain that links dendriti

207 This structure provides insights into the architectural principles governing ligand recognition, h

208 toolbox for the assessment and comparison of architectural properties in brain networks.

209 isation markedly diminishes all investigated architectural properties of cortical connectivity.

210 connected microchannels which replicates the architectural properties of microvascular systems.

211 through which we can study the higher-order architectural properties of the world around us.

212 hromosomal DNA based on its two distinct DNA architectural properties.

213 ions containing active genes and clusters of architectural protein binding sites.

214 hromatin topology is in part mediated by the architectural protein CCCTC-binding factor (CTCF) that b

215 The architectural protein CTCF plays a complex role in decod

216 on of progerin, a mutant form of the nuclear architectural protein lamin A, leading, through unknown

217 a support a model suggesting that the unique architectural protein occupancy within enhancers is one

218 h mobility group box protein 1 (HMGB1) is an architectural protein that facilitates the formation of

219 ults support a model in which YY1 acts as an architectural protein to connect developmentally regulat

220 sis for the functional switch from chromatin architectural protein to transcription factor and DNA da

221 CTCF is an architectural protein with a critical role in connecting

222 Thus, an architectural protein with no discernible DNA sequence-r

223 placenta-specific occupancy of the chromatin architectural protein, CTCF, at HSIV.

224 nds, consistent with its role as a chromatin architectural protein.

225 Chromatin architectural proteins (CAPs) bind the entry/exit DNA of

226 ions for long-range contacts involving known architectural proteins and DNA motifs.

227 are enriched for RNA Polymerase II, CBP, and architectural proteins but there are also distinctions.

228 oss the genome are maintained in part by the architectural proteins CCCTC binding factor (CTCF) and t

229 res associated with active promoters and the architectural proteins CTCF and YY1.

230 gether, our data identify Nups as a class of architectural proteins for enhancers and supports a mode

231 temperature stress induces relocalization of architectural proteins from TAD borders to inside TADs,

232 cy, long non-coding RNAs, or the presence of architectural proteins have been implicated in regulatio

233 Architectural proteins insulate compartmental domains by

234 Chromatin architectural proteins interact with nucleosomes to modu

235 molecules randomly decorated by nonspecific, architectural proteins into tightly organized 3D structu

236 atin fibers by association with histones and architectural proteins such as high mobility group (HMGB

237 ors that regulate lineage specification, the architectural proteins that globally coordinate DNA meth

238 ory elements and siRNA-mediated depletion of architectural proteins to determine the relative contrib

239 o gain and retain physical interactions with architectural proteins upon stimulation with ecdysone.

240 wo enhancer classes are occupied by distinct architectural proteins, affecting their enhancer-promote

241 tion and activity of cell signaling enzymes, architectural proteins, and immune regulatory factors.

242 is partly established by a special class of architectural proteins, of which CCCTC-binding factor (C

243 By evaluating ChIP-seq occupancy of architectural proteins, typical enhancer-associated prot

244 tional compensation among nucleosome binding architectural proteins.

245 of transcription or depletion of individual architectural proteins.

246 ng axon trafficking parameters, and imposing architectural rearrangements such as the nodes of Ranvie

247 Intracellular Domain (NICD) blocked cardiac architectural regeneration and restoration of ventricula

248 Critical chromatin architectural regulators condensin I and condensin II pl

249 the estimation of Pueblo population based on architectural remains and apply this formula to 18 archa

250 ation of H2'-H3 sequences suggests that this architectural remodeling constitutes a previously unreco

251 This article reviews the extensive architectural remodeling that occurs within lymph nodes

252 e arc formation in lamellipodium-to-lamellum architectural remodeling.

253 steady-state junctions entails a process of architectural reorganization whereby filaments that are

254 -cadherin-dependent fashion to support actin architectural reorganization, contractility, and extrusi

255 al plasticity of a human tRNA synthetase for architectural reorganizations that are preferentially el

256 We investigated the architectural response of fine roots exposed to 14 yr of

257 nd leaf mass per area, are the stereotypical architectural responses to foliar shade in the shoot.

258 on within Arabidopsis to look for novel root architectural responses to low K.

259 We report a novel architectural role for 53BP1 in Igh chromatin looping in

260 iative fear learning, and unravel a distinct architectural rule for synapse formation in the adult br

261 uately studied to test alternative hydraulic architectural rules such as da Vinci's rule or Murray's

262 diac extracellular matrix (ECM) provides the architectural scaffold to support efficient contraction

263 s consisting of lipid or polymer vesicles as architectural scaffolds and of membrane and soluble prot

264 ggers a switch between two different nuclear architectural schemes during Arabidopsis postembryonic d

265 The architectural similarity between RAG1 and the hairpin-fo

266 ) transcription factor activation that shows architectural similarity to endoplasmic reticulum-associ

267 crystal structure of FimU revealed striking architectural similarity to its T2S ortholog GspH, despi

268 ented here demonstrate that, despite overall architectural similarity to LdtMt2, the LdtMt5 active si

269 ibosomal intermediates in close proximity to architectural sites such as an RNA duplex formed by the

270 ds on their mechanical performance and micro-architectural stability while deployed under long-term m

271 Such neuroprotective architectural strategies may be conserved, to a lesser e

272 there may be some beneficial effect from the architectural structure of the vitreous that enhances ev

273 regulatory enhancer regions to a subnuclear architectural structure that serves as an underlying mec

274 of neural activity associated with specific architectural styles in several high-level visual brain

275 y, the network of brain regions representing architectural styles included the fusiform face area (FF

276 scenes at a subordinate-level, in our case, architectural styles of buildings.

277 eural correlates of the visual perception of architectural styles stem from style-specific complex vi

278 much larger extent in the neural encoding of architectural styles than entry-level scene categories.

279 applications in biomedical devices, adaptive architectural systems, robotics and energy harvesting.

280 he fabrication of nanoscale devices requires architectural templates on which to position functional

281 utant p53 GOF activity in clonogenic growth, architectural tissue remodeling, migration, invasion, an

282 t accurate estimates of this biomass-related architectural trait.

283 er tool is provided to recover a rich set of architectural traits from RootNav's core representation.

284 ith certain leaf surface, morphological, and architectural traits that reduce leaf wettability.

285 litates the systematic investigation of root architectural traits, in particular with respect to the

286 In the case of root architectural traits, this limits phenotyping efforts, l

287 s studies from our laboratory identified the architectural transcription factor and oncogene, high mo

288 High Mobility Group A2 (HMGA2), an architectural transcription factor, is known to regulate

289 adal ridge, is initiated by SRY, a Y-encoded architectural transcription factor.

290 termination is initiated by SRY, a Y-encoded architectural transcription factor.

291 These architectural transformations present an entirely new ap

292 gen IV enabled the assembly of a fundamental architectural unit for multicellular tissue genesis.

293 ction, the characterization of RNA's modular architectural units is required.

294 e conclude that ghost fibers are autonomous, architectural units necessary for proportional regenerat

295 diversity as well as environmentally induced architectural variation of both monocot and dicot plants

296 tein kinase A signaling underlie much of the architectural variation we observe in colony biofilms.

297 to modified maturation schedules underlying architectural variation.

298 we propose underlies similar cases of plant architectural variation.

299 Although there are countless architectural variations among the ICUs, all can be clas

300 condition, shedding light on their observed architectural variations.