ライフサイエンスコーパス: architectural

1 implications in many diverse fields such as architectural acoustics and biomedical engineering.

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

3 estigate cognitive processes associated with architectural affordances, we used a mobile brain/body i

4 Aging manifests with architectural alteration and functional decline of multi

5 We measured seedling leaf, architectural and biomass distribution traits of 18 New

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

7 re, we discuss recent findings regarding the architectural and dynamic diversity of the immunological

8 Control over the architectural and electronic properties of heterogeneous

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

10 Here, using a range of architectural and immunohistochemical stains, we describ

11 Using architectural and immunohistochemical stains, we observe

12 Using architectural and immunohistochemical stains, we observe

13 gaps greater than 1 nucleotide (nt) pose an architectural and logistical problem for the two domains

14 at preventing most decrements in bone micro-architectural and mechanical properties due to hindlimb

15 rganisms of the same species show remarkable architectural and often local wiring similarity, raising

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

17 ere we review the environmentally regulated, architectural and regulatory roles of nucleoid-associate

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

19 I-visible tumors appear to exhibit increased architectural and vascular density compared to mpMRI-inv

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

21 sposase and CRISPR-Cas integrase are largely architectural, and it appears that evolutionary change i

22 varia, as they are baked in by cookie-cutter architectural approaches to facility design.

23 demonstrate that nuclear speckles provide an architectural basis for nuclear homing of HIV-1 replicat

24 These findings provide an architectural basis for the understanding of the dynamic

25 s among individual cells mediate large-scale architectural biofilm arrangements and provide spatial p

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

27 nals and act as a functional, rather than an architectural bridge, between promoters and enhancers.

28 This architectural change facilitates cognate promoter-enhanc

29 s an evolving and inhomogeneous histological/architectural change that progresses through different s

30 bouts of accelerated sequence evolution and architectural changes (e.g. a loss of introns andRNA-edi

31 or to IL-13 exposure abrogated IL-13-induced architectural changes and esophageal barrier dysfunction

32 E2 attenuated IL-13-induced architectural changes and esophageal epithelial barrier

33 and affected individual podocytes displayed architectural changes associated with migration defects

34 redox properties, demonstrating that subtle architectural changes can dramatically alter metal utili

35 sfunction that correspond with early macular architectural changes characteristic of multiple scleros

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

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

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

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

40 In parallel, transcriptional and architectural changes of this region were observed inclu

41 es of the excised sclera revealed no scleral architectural changes or abnormal deposits.

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

43 attachment zone length and is accompanied by architectural changes to the anterior cell end.

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

45 er than skin-specific, phenomenon reflecting architectural changes, i.e. a shift in the extracellular

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

47 n 3D constructs to mimic the intrinsic micro-architectural characteristics of native tissues.

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

49 g of all active genes bound by Pol I and the architectural chromatin protein Upstream Binding Transcr

50 ing mitosis and reveals that CTCF sites, key architectural cis-elements, display cell cycle stage-dep

51 single bound nucleotide, which may act as an architectural co-factor to stabilize a protein-protein i

52 present the most important considerations in architectural coating design.

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

54 However, the architectural complexity and heterogeneous contents asso

55 Their architectural complexity and size impose specific demand

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

57 y methodology is able to efficiently enhance architectural complexity for calix[4]resorcinarene-conta

58 tition strategies to preserve fitness as its architectural complexity increases during morphogenesis.

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

60 Our data link architectural complexity to transcriptional kinetics and

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

62 ), significantly reducing the gate count and architectural complexity, but thus far it has not been p

63 engineered tissues have been constrained in architectural complexity, owing to the limitations of ex

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

65 ovement in performance observed with various architectural components in the authors' approach.

66 urces, cellular signaling molecules, and key architectural components of complex lipids.

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

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

69 alization concept is postulated to act as an architectural constraint on the evolution of molluscan s

70 ng, suggesting that the inputs, outputs, and architectural constraints imposed were sufficient for re

71 The architectural constraints that dictate the formation of

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

73 Architectural contributions of RNA to cytosolic signalin

74 Metallomacromolecular architectural conversion is expanded by the characteriza

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

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

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

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

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

80 Previous studies have evaluated the architectural designs and mechanical properties of diffe

81 u mechanical testing, we identify multiscale architectural designs within the exoskeleton of this bee

82 tion light detection and ranging reveals the architectural details of an ancient settlement on the Gu

83 To investigate the architectural determinants of this phenotype, we used ab

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

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

86 ce hydrological retention, attributed to the architectural differences in the roots of these macrophy

87 The results highlight the architectural differences with motile cilia and provoke

88 Our architectural dissection reveals the mode of association

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

90 Parenchymal sequelae included fibrosis with architectural distortion and volume loss (90%), cavities

91 The rate of architectural distortion biopsies was 2.0% (13 of 643) w

92 ter detect "grouped microcalcifications" or "architectural distortion" lesions (referred to as calcif

93 was performed were noncalcified lesions (eg, architectural distortion, asymmetry, and mass) than for

94 nifesting as contracting consolidation, mild architectural distortion, intralobular lines, lobular di

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

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

97 groups of calcifications (12 malignant), 18 architectural distortions (15 malignant), and five asymm

98 In addition, more architectural distortions and asymmetries are amenable t

99 o the higher number of spiculated masses and architectural distortions found at DBT (P < .001 for den

100 tal breast tomosynthesis-guided biopsy, more architectural distortions were biopsied, more radial scl

101 cancers classified as spiculated masses and architectural distortions.

102 e 34 discordant DBT-guided biopsies, 30 were architectural distortions.

103 Significant cingulum architectural disturbances were observed in traumatic br

104 ate reconstruction we identify two stages of architectural diversification.

105 ovide a framework for mechanistic studies of architectural diversification.

106 c pLGICs; however, they often encode greater architectural diversity involving additional amino-termi

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

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

109 We chart NLR architectural diversity, identify new architectures, and

110 to travel along DNA in the presence of other architectural DNA binding proteins using single-molecule

111 Our results suggest that architectural dynamics may influence jaw-muscle performa

112 copy and image analysis, we investigated the architectural dynamics of rhodamine-phalloidin stabilize

113 ody of theoretical work has proposed how the architectural elements and various cell types of the DG

114 try (central and conformational) provide new architectural elements of facile atroposelective constru

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

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

117 in access at poised enhancers and chromosome architectural elements.

118 re mostly realized through the strategies of architectural engineering to accommodate mechanical stre

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 hromosomal rearrangements or perturbation of architectural factors.

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

124 hora silk moth species vary significantly in architectural features and in the level of intraspecific

125 These architectural features are conserved in the yeast and ba

126 Because functions may depend on architectural features at different scales, network arch

127 ranularity to address potentially prognostic architectural features beyond Gleason patterns.

128 milar tumor growth dynamics and retention of architectural features for 28 days.

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

130 the cell nucleus arises from a wide range of architectural features including DNA loops, chromatin do

131 te the use of persistent homology to capture architectural features independently of Gleason patterns

132 because brain organoids better recapitulate architectural features of a developing brain than 2D cul

133 ue equivalents, which are built to replicate architectural features of biopsied CRC tissue.

134 We first characterized and compared the architectural features of cocoons at all three cocoon se

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

136 drogel scaffold replicate the functional and architectural features of in vivo crypts.

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

138 Both compartments recapitulate stable architectural features of native tissue and the ability

139 en the histological features quantifying the architectural features of neoplasia on a microscopic sca

140 l drug targets, it is essential to chart the architectural features of SARS-CoV-2 and pinpoint region

141 a mechanism by which glycolysis responds to architectural features of the actomyosin cytoskeleton, t

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

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

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

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

146 Crystallographic analysis reveals architectural features that promote enhanced biochemical

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

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

149 of the spindle machinery relies on conserved architectural features, such as focused poles, chromosom

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

151 nship between transcription reactivation and architectural features.

152 Morphological and architectural fine-root traits were measured on individu

153 ial functional role for the different cocoon architectural forms.

154 Together, our results provide an architectural framework for sDAPs that sheds light on fu

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

156 ure dynamics (changes in muscle shape or the architectural gear ratio) during the gape cycle while su

157 hypothesized and found three interdependent architectural gradients underlying the organization of i

158 of clustering prostate cancer histology into architectural groups through a ranked persistence vector

159 persistent homology to identify specific sub-architectural groups within single Gleason patterns, sug

160 y filamentous fungi is often a threat to the architectural heritage (i.e. tombs and historic sites).

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

162 across 11 chromosomes, and characterized its architectural impact.

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

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

165 Architectural integrity of the mitotic spindle is requir

166 f microtubule triplets, as well as centriole architectural integrity remain poorly understood.

167 y rich dynamic behavior without losing their architectural integrity.

168 ns of meters, has made the imaging of entire architectural interior feasible.

169 y to integrate combinations of RNA motifs as architectural joints and DNA building blocks as function

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

171 This architectural map explains the vast majority of the elec

172 CF/cohesin-dependent and -independent genome architectural mechanisms might regulate compaction and r

173 The extracellular matrix (ECM) provides an architectural meshwork that surrounds and supports cells

174 Thus, H3K9me2 acts as a 3D architectural mitotic guidepost.

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

176 D3P couples the Architectural model of DEvelopment based on L-systems (A

177 ctron cryotomography map produced a complete architectural model of the intact T2SS that provides ins

178 chroism spectroscopy are consistent with our architectural model.

179 Scale-free architectural models propose that cognition has the same

180 tigations into neuropsychologically-relevant architectural modifications across systematic reductions

181 ross a range of magnitudes without requiring architectural modifications.

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

183 They are specifically directed at architectural motifs in BC RNA 5' stem-loop domains that

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

185 e proposed method will enable new studies of architectural order at spatial scales ranging from organ

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

187 ucture sites, with associated changes in the architectural organization and depth of lamination withi

188 The architectural organization of chromatin can play an impo

189 of larger vacuoles and cysts, changes in the architectural organization of cortical structures, aberr

190 ach to study their molecular control and bio-architectural organizations.

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

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

193 ized by vascular spaces, the macrotrabecular architectural pattern, and a lack of immune infiltration

194 logy images into unique groups with dominant architectural patterns consistent with the continuum of

195 the morphology of cancer into five distinct architectural patterns, labeled 1 to 5 in increasing lev

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

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

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

199 Root architectural plasticity traits were related to 13 (Aus

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

201 The NPC has also been viewed as a nuclear architectural platform that impacts genome function and

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

203 l of Msp1's mechanism, which follows general architectural principles established for other AAA prote

204 stant metabolosome shell, implying universal architectural principles for bacterial microcompartment

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

206 Here we identified which architectural principles of functional connectome organi

207 We delineate architectural principles on several hierarchical organiz

208 Our work elucidates the architectural principles that underpin the assembly of t

209 These circuit-specific architectural profiles related to individual differences

210 lf-association of nucleoid proteins on their architectural properties and try to determine whether di

211 These so-called architectural properties of nucleoid proteins are still

212 ensive evaluation of the heterogeneous micro-architectural properties of the human femoral head, high

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

214 in itself not sufficient to understand their architectural properties.

215 s on cell size and shape, as well as biofilm architectural properties.

216 teractions and enriched for occupancy of the architectural protein CCCTC binding protein (CTCF).

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

218 knockout of Chd4 promotes recruitment of the architectural protein complex cohesin preferentially to

219 me positioning, and chromatin binding of the architectural protein CTCF play an important role for es

220 perturbed cells, we demonstrated that genome architectural protein CTCF prevents excessive clustering

221 The high mobility group box (HMGB) architectural protein family has been well studied in th

222 ambda from the chromosome, the bacterial DNA architectural protein Fis recruits multiple lambda-encod

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

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

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

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

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

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

229 binding sites for transcription factors and architectural proteins and are thought to play an import

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

231 Chromatin-associated architectural proteins are part of a fundamental support

232 s supported by a change in the enrichment of architectural proteins at TAD borders, with BEAF-32 pres

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

234 Here, we engineer a new class of synthetic architectural proteins for directed rearrangement of the

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

236 tion maps, and genome-wide occupancy data of architectural proteins have revealed that genome topolog

237 Architectural proteins insulate compartmental domains by

238 tive elements, epigenetic modifications, and architectural proteins interact ensuring proper genome e

239 ound that multimerized binding sites for the architectural proteins Pita, Su(Hw), and dCTCF function

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

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

242 in 153 (NUP153) interacts with the chromatin architectural proteins, CTCF and cohesin, and mediates t

243 These include binding sites for architectural proteins, such as CTCF, RAD21, and SMC3, t

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

245 th the expression levels of several of these architectural proteins.

246 latory DNA, a topological activity requiring architectural proteins.

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

248 er, embryonic cells had undergone remarkable architectural rearrangements.

249 Herein, we present the architectural redesign of RCSB PDB data delivery service

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

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

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

253 l roles of a RhoGEF-anillin module in septin architectural remodeling during cytokinesis at the filam

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

255 ruption of H1 function results in a profound architectural remodelling of the genome, which is charac

256 Together, our findings present architectural renderings of the DNA conjugation or "mati

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

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

259 n of bacterial origin, has converged onto an architectural role filled by histones in other archaea.

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

261 ersity or for partitioning of functional and architectural roles.

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

263 icates a structured three-way junction as an architectural scaffold to pre-organize helical domains f

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

265 istics in all cases and displayed particular architectural scenarios (which we arbitrarily subdivided

266 also revealed endocrine cell allocation and architectural similarities between pig and human islets.

267 of marginal posteriors at the expense of the architectural simplicity of variational message passing.

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

269 ous-lipid environment is integrated with the architectural stability, structure and function of gap j

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

271 biofilm matrix; instead, filamentous biofilm architectural strength appears to derive at least in par

272 Architectural stripes appear to be driven by enhancer ac

273 Furthermore, we show that architectural stripes are a frequent feature of developm

274 asymmetric regions of contact, the so-called architectural stripes(3).

275 PmDscam has a conserved architectural structure consisting of an extracellular r

276 ction of HSV-1 with the complex cellular and architectural structure of the human CNS.IMPORTANCE This

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

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

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

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

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

282 We evaluate prostate cancer for architectural subtypes using techniques from topological

283 Our resulting architectural switch model explains why the human Fe-S a

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

285 B-box motifs physically associated with the architectural TFIIIC complex and with other factors incl

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

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

288 variation modulating agronomically important architectural traits enriched specifically near dynamica

289 Phenotyping Platform" (D3P), to access crop architectural traits from HTP observations.

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

291 fewer correlations between root diameter and architectural traits.

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

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

294 These architectural transformations present an entirely new ap

295 In this review, we focus on the architectural transformations that lead to a profound re

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

297 rkable conservation of contact sites despite architectural variation.

298 we propose underlies similar cases of plant architectural variation.

299 th America and investigated the evolution of architectural variation.

300 pen our appreciation of the small scaffold's architectural versatility and also reveal lucrative oppo