ライフサイエンスコーパス: architecture

1 different environments hinges on its genetic architecture.

2 t of the formation of the active site on RNP architecture.

3 ought to characterize the subfields' genetic architecture.

4 ms, embedded in a dynamic, recurrent circuit architecture.

5 over crops characterized by different canopy architecture.

6 ructural arrangement, stability, and overall architecture.

7 ALI-induced proteolytic collapse of arterial architecture.

8 rs on broad dimensions of variation in brain architecture.

9 erturb gene regulation by altering chromatin architecture.

10 ters evolved from a shared ancestral genetic architecture.

11 tanding the structure of cortical functional architecture.

12 e known stability of fMRI-based intrinsic FC architecture.

13 ro-pyrazinones" featuring a hetero-tricyclic architecture.

14 ed FAPI crystallites which form a mesoporous architecture.

15 in homeostasis and the regulation of nuclear architecture.

16 unted for the majority of dynamic changes in architecture.

17 lator of IRF8 silencing, affecting chromatin architecture.

18 icroscopy that revealed a heptameric channel architecture.

19 embership in protein complexes, and promoter architecture.

20 nation, indicating a much more rigid protein architecture.

21 he organizer for the local three-dimensional architecture.

22 urons displayed spine loss and altered spine architecture.

23 the known genetic networks for branching and architecture.

24 m metal batteries can be overcome using this architecture.

25 , the nervous system transitions to a stable architecture.

26 ene toward a spatially resolved 2D-patterned architecture.

27 a theoretical framework to justify our model architecture.

28 of population-specific components of genetic architecture.

29 e result of, A. fumigatus late-stage biofilm architecture.

30 s have provided insights into the overall NC architecture.

31 ling without grossly disrupting the cellular architecture.

32 because they appear to have distinct genetic architecture.

33 trongly controlled by 3D variations in fault architecture.

34 lds into an evolutionarily conserved modular architecture.

35 tion and being implemented by distinct brain architectures.

36 equires more efforts in developing cognitive architectures.

37 nges on the organization of dynamic activity architectures.

38 groups and with precisely defined nanoscale architectures.

39 ) shell can be beneficial for various sensor architectures.

40 complex and heterogeneous internal vascular architectures.

41 chies of deep neural networks with different architectures.

42 ecision and state spaces and model-free (MF) architectures.

43 model is valid for a broad range of genetic architectures.

44 integration of 2D COFs into thin-film device architectures.

45 rmation elements in future spintronic device architectures.

46 lows for assembling 3D clusters with complex architectures.

47 sting biophysical features into higher-level architectures.

48 onstruct highly sophisticated supramolecular architectures.

49 acellular matrix and cells, and tissue-level architectures.

50 closely resemble natural polyhedral protein architectures(7,8) and are, to our knowledge, unique amo

51 ly, this complex adopts a dimeric structural architecture, accounting for PRC2 self-association that

52 wn that men and women have different genetic architectures across many traits.

53 onsiveness to theoretically any nucleic acid architecture, addressing a significant need in synthetic

54 We show that every balanced network architecture admits stimuli that break the balanced stat

55 -level organization confers to ASFV a unique architecture among the NCLDVs that likely reflects the c

56 tantial SCNA and methylation ITH, and clonal architecture analyses present congruent evolutionary tra

57 In situ molecular architecture analysis of organelles and protein assembli

58 es a minimal conserved ECF sigma(2)-sigma(4) architecture and an additional C-terminal extension that

59 With a tailored architecture and an ensemble approach to CNN parameter i

60 We review recent data to understand rosette architecture and apply maxims derived from computational

61 , a cardinal sign of disrupted mitochondrial architecture and bioenergetics.

62 ion, RNA polymerase, is conserved in general architecture and catalytic function across the three dom

63 We cover the molecular architecture and catalytic mechanisms that distinguish S

64 ting technologies can enable the creation of architecture and devices with an unprecedented level of

65 testine-Chip that emulates intestinal tissue architecture and functions, that are relevant for the st

66 In vivo interrogation of chromatin architecture and genome-wide RALY-binding pattern reveal

67 nd regulate many agronomic traits, including architecture and grain yield.

68 g protein that maintained actin cytoskeleton architecture and helped KEAP1 to sequester NRF2 in the c

69 personal factors, and lastly, (C) cognitive architecture and human nature that impacts all of us.

70 g motifs potentially beneficial for enhancer architecture and immune functions were particularly freq

71 ptosis gene RIPK3, show disturbed bone micro-architecture and increased osteoclast number, highlighti

72 tions has provided deep insights into memory architecture and its neural underpinnings.

73 ated, which kinetics vary with the composite architecture and last beyond optical pulse temporal char

74 ductive isolation, research into the genetic architecture and molecular basis of its evolution contin

75 The genetic architecture and neurogenetics of animal migration remai

76 Despite similarities in their overall architecture and phosphate binding motif, a lack of sequ

77 However, LOAD genetic architecture and prediction are unclear.

78 ucture reveals atomic-level detail in capsid architecture and provides important guidance for the des

79 Despite marked variation in tissue architecture and regenerative demands, SCs often follow

80 w classes of glioma differ in their cellular architecture and relate the observed cellular states to

81 onents, leading to the deterioration of lung architecture and respiratory functions.

82 in multiple populations and compared genetic architecture and the effect of natural selection on thes

83 to determine the epigenetic state, 3D genome architecture and transcriptional landscape of engram cel

84 , the root growth, leaf width, inflorescence architecture and/or floral development were affected.

85 isadvantages associated with different probe architectures and describe the advances enabled by these

86 ly of soft functional materials with tunable architectures and distributed functionalities.

87 racking can be achieved by canonical network architectures and dynamics, and that the resulting respo

88 ubtractive process for creating novel device architectures and improving the structural and optical q

89 rt vital bodily functions, yet their genetic architectures and involvement in common brain disorders

90 Here we introduce a modular barrel architecture, and demonstrate hierarchical assembly of a

91 vo We particularly focus on the composition, architecture, and physical properties of the OM and how

92 D scaffolds to mimic anatomical size, tissue architecture, and tissue-specific functions.

93 lack of knowledge regarding their structural architecture, antifungal activity, and modes of action a

94 col for absolute quantification of chromatin architecture (AQuA)-HiChIP, an advance that allows the a

95 how genetics, epigenetics, and the 3D genome architecture are coordinated in the aberrant gene expres

96 Anatomically, ductal morphogenesis and organ architecture are minimally perturbed in Jag1 mutants unt

97 resulting changes in chromatin rheology and architecture are required to insulate genetic material f

98 We show that deep-learning architectures are capable of producing false-positive ra

99 Since most dramatic changes in genomic architectures are caused by genome rearrangements, this

100 Such oligomeric architectures are found in several other electron transf

101 nveils the structure of the liver blood flow architecture as a combination of superimposed tree-shape

102 mmalian lipins function with the same domain architecture as Tt Pah2.

103 l actin assembly and perturbed lamellipodial architecture, as evidenced by changed network geometry a

104 dentify de novo cell-type-specific chromatin architectures associated with gene expression, as well a

105 We use this approach to study chromatin architecture at high spatial and temporal resolution thr

106 In particular, we propose a plausible brain architecture based on assemblies for implementing the sy

107 Here we report differences in genetic architecture between depression defined by minimal pheno

108 ayers, polymer ordering, polymer nanopores), architecture (branched vs linear), functional groups (co

109 ging to separate structural components of an architecture built from-thus held together by-a continuo

110 e can be achieved via the site-specific mesa architecture, by enabling generation of multineutral lay

111 A star-shaped DNA architecture, carrying five molecular beacon-like motifs

112 We characterized the fibrosis (amount, architecture, cellular components, and ultrastructure) i

113 alterations of the peri-implant soft tissue architecture characterized by an apical discrepancy of t

114 hat the SWAI population has distinct allelic architecture compared to populations of European and Eas

115 By modulating LbL composition and architecture, component release profiles in the skin cou

116 Thanks to their hierarchically porous architecture, compositional and structural tunability, a

117 addition to establishing mitotic chromosome architecture, condensin-mediated long-range chromatin in

118 and crustaceans is based on the compound-eye architecture, consisting of a dense array of individual

119 el printing enables production of volumetric architectures containing desired structures using progra

120 aternary structure, and distinct active site architecture despite overall structural similarity.

121 tion of recurrently mutated genes and clonal architecture differed among MDS/MPN subtypes.

122 -level analysis showed ligand binding pocket architectures differences in size, shape and electrostat

123 In addition to myocardial architecture disruption, this effect can be attributed t

124 vidence that the lack of a specific cortical architecture does not hinder advanced cognitive skills.

125 Limited insights into their molecular architecture, due to the sheer size and the insoluble ch

126 hstand high pressure and maintain its porous architecture during electrode calendering.

127 We collected data on architecture dynamics (changes in muscle shape or the ar

128 However, the fabrication of architectured electrodes often involves multiple laborio

129 Its open architecture enables any tool or pipeline to output or c

130 between ecological interactions and network architectures exists, but cannot be fully understood wit

131 ly achieving high energy densities, yet this architecture faces challenges arising from interfacial i

132 pture high-level structural features such as architectures, folds and conformity to conserved structu

133 duct length ratio) as the entire blood flow architectures follow the principle of equipartition of i

134 d bilayer graphene using a back-gated device architecture for angle-resolved photoemission measuremen

135 This study reveals a striking zonal architecture for the transitional hourglass that pre-pat

136 and explore a quantitative atlas of cellular architecture for the zebrafish posterior lateral line pr

137 offers new opportunities for designing such architectures for a broader range of catalytic applicati

138 We then identified permissive architectures for minimal synthetic plant promoters enab

139 results argue that this illusion arises from architectures for motion detection that are shared acros

140 zoa and the preservation of conservative NOS architecture from prokaryotic ancestors.

141 NSPR), across a range of cellular and tissue architectures, from mitochondrial networks and nuclear p

142 uce novel kinds of symmetric self-assembling architectures, from protein cages to extended two-dimens

143 Gestalt theory may explain why rodent islet architecture has historically been seen as having a core

144 control over the bulk geometry and internal architecture has situated 3D printing as an attractive f

145 on of 10 conserved core proteins within this architecture have been elucidated.

146 teria used by experts to evaluate sarcomeric architecture have not been well-defined.

147 Model approaches to nuclear architecture have traditionally ignored the biophysical

148 Designing out-of-equilibrium architectures, however, requires a more subtle control o

149 t molecular impact correlates with subclonal architecture (i.e., early versus late mutations), and di

150 lopment will enable the improvement of plant architecture in agriculture.

151 uates serum factors that protect foveal MPOD architecture in Caucasian offspring of parent(s) with AM

152 omplexity and dynamic nature of 3D chromatin architecture in human acute leukemia.

153 rom nanoparticles to organelle-like hydrogel architecture in living cells.

154 describe an approach to large-scale nuclear architecture in metazoans that incorporates cell-type-sp

155 c pathway, and the role of metabolic network architecture in optimizing its function.

156 an electrolyte solution in a closed sandwich architecture in order to study the photo-response of pho

157 The reconfiguration of community architecture in the brain provides fruitful information

158 ated as separate monomers) against a monomer architecture in which the catechol and amine were couple

159 vance of brainstem regions and their genetic architectures in common brain disorders.

160 vital for the construction of organelle-like architectures in living cells, but has proven difficult

161 There are clear roles for branched architectures in regulating proteasome-mediated degradat

162 folding and multiplexed imaging of nucleome architectures in single cells of several important biolo

163 ocessing is envisioned to outperform digital architectures in specific tasks, such as image processin

164 llular matrix (ECM) fibers and ordered micro-architecture induced an epithelial phenotype in CRC cell

165 ectron transfer (ET) complexes, but how this architecture influences activity is unclear.

166 Such modular architecture is common among cell-cycle proteins; thus,

167 re, thus demonstrating that the overall AHAS architecture is conserved across kingdoms.

168 , have been implicated; however, the genetic architecture is poorly understood.

169 Here, an all-scale hierarchical architecture is proposed and demonstrated to achieve hig

170 itional advantage of our fully convolutional architecture is that it allows for training on small dom

171 eir exact topology or a particular chromatin architecture, is the key factor.

172 nvestigation of each region of the molecular architecture led to the identification of N-[1-(3-fluoro

173 that no other macro- and microphysiological architecture metrics of sleep demonstrated such sensitiv

174 H (MERFISH), multiplexed imaging of nucleome architectures (MINA), and sequential single-molecule RNA

175 Key architectures obtained through NCA ROP or in combination

176 integrative modeling to determine an in-cell architecture of a transcribing and translating expressom

177 ral studies have revealed the supramolecular architecture of a variety of disease-associated amyloids

178 These results demonstrate that the genetic architecture of alcohol consumption only partially overl

179 c known gnathostomes, and the shared cranial architecture of arthrodire placoderms, maxillate placode

180 matrix and are required for the assembly and architecture of biofilms produced by a wide variety of m

181 not recapitulate the three-dimensional (3D) architecture of brain tissue.We employed human induced p

182 heir heterogeneity, and enabled the cellular architecture of breast cancer tissue to be characterized

183 The genomic architecture of carcinomas, sarcomas and lymphomas arisi

184 ty and has yielded insights into the genetic architecture of complex traits.

185 and thereby shed light on the computational architecture of cortex.

186 fer further insight into the complex genetic architecture of cross-cancer susceptibility.

187 The genetic architecture of each individual comprises common and rar

188 even cancer cell lines to reveal the complex architecture of ecDNA, a breakage-fusion-bridge and othe

189 Inferring the genetic architecture of evolution in the fossil record is diffic

190 However, the invalid 2D architecture of fabric limits the application in thermoe

191 highlight the potential significance of the architecture of GalNAc conjugation for efficient uptake

192 topic maps, expressed by a uniform blob-like architecture of hue responses within each area.

193 and provide a new global perspective on the architecture of human gene regulation.

194 rehensive analyses revealed distinct genetic architecture of human NP and AF compartments and identif

195 of the least studied aspects of the genetic architecture of human traits and diseases.

196 genes paved a path to understand the genetic architecture of husk in maize.

197 hmark for future studies linking the genetic architecture of individual and mental health traits with

198 genetics of an organism to the reproducible architecture of its connectome, offering experimentally

199 Our findings highlight an unusual genetic architecture of MN, with four loci and their interaction

200 The structure reveals an overall architecture of mouse DHX36 that is similar to previousl

201 this work elucidates the previously unknown architecture of pannexin channels and establishes a foun

202 , and thus little is known about the genetic architecture of phenotypic variation in these population

203 ions is a consequence of the dynamic modular architecture of Pin1.

204 understanding of the genetic and epigenetic architecture of reaction severity in peanut allergy.

205 To understand how the genetic architecture of resistance varies across time and geogra

206 However, the architecture of septin higher-order assemblies and their

207 NCE STATEMENT We show that the complex micro-architecture of sleep-stage/arousal transitions arises f

208 erences, a finding that supports a polygenic architecture of species boundaries.

209 ndicates a mechanism essential for the micro-architecture of spontaneous sleep-stage and arousal tran

210 t into substrate and product binding and the architecture of the active sites, disclosing important s

211 their pathophysiology and the computational architecture of the cognitive processes they target.

212 ticle cryo-EM to reveal the organisation and architecture of the complete human TSCC.

213 In order to understand the computational architecture of the cortex, we need to investigate the w

214 mmary, these results disclose the structural architecture of the free forms of thrombin and prethromb

215 ein complex that is essential for the proper architecture of the mitochondrial inner membrane.

216 While the general architecture of the neural network and the intrinsic pro

217 The structural architecture of the northern South China Sea continental

218 r if such observation is a limitation of the architecture of the palette of materials available in na

219 ics of most neurons define a shallow network architecture of the pharyngeal connectome.

220 the target system state on a fixed hardware architecture of the quantum computer.

221 verall, these characterizations revealed the architecture of the SARS-CoV-2 virus in exceptional deta

222 Architecture of the SAT varied with phases of the gape c

223 This structure highlights differences in the architecture of the T4aP secretin from the type II and t

224 The overall architecture of the T4aPM and the location of 10 conserv

225 Characterising the circuit architecture of these diseases could illuminate both the

226 the process of immune exclusion, shapes the architecture of these microbiomes.

227 as to examine the three-dimensional collagen architecture of wounded embryonic corneas, whilst identi

228 introduce the fundamentals and typical model architectures of DL.

229 DHX36 that is similar to previously reported architectures of fly and bovine DHX36.

230 The micro or nanoscale architectures of these structures significantly affects

231 ectrometry (MS) reveals that the modular OGD architecture offers the ability to control protein purif

232 We discuss the influence of promoter architectures on decision times and error rates, present

233 solution descriptions of archaeal chromosome architectures, our data provide evidence of multiple mod

234 Most materials, both natural as well as architectured, possess crystalline symmetries.

235 The proposed 3D-MCN architecture predicted lung nodule malignancy with a hig

236 ary structure, it maintains a compact global architecture primed for SUMO interaction.

237 e observed differences in A. cahirinus sleep architecture raise questions about the evolutionary driv

238 ar processes, notably gene regulation, while architecture related alterations, such as translocations

239 tomation for task-related functional network architecture remains far from understood.

240 icrobial community across the intact biofilm architecture remains sparse.

241 which discrete NPs are assembled into chiral architectures, represent an exciting and growing class o

242 ndicate that revealing sex-dependent genetic architecture requires the consideration of temporal proc

243 surface diffusion, preventing generation of architecture resembling late developmental stages.

244 The naturally designed architecture, semi-permeability, and catalytic improveme

245 o pairs of imine-based metallosupramolecular architectures (sharing no component) each with a [2 x 2]

246 tant also displayed defects of the cell wall architecture, suggesting GPI7 is required for cell wall

247 This scale-free architecture supports representations with diverse funct

248 2 and NEMF), despite their relatively simple architecture, synthesize such C-terminal tails in the ab

249 series of peptoids (PE1-9) with two types of architectures, termed as "brush" and "block," were built

250 s complements the diverse maps of regulatory architecture that comprise the ENCODE Encyclopedia, and

251 Gingival epithelial cells form an anatomic architecture that confers defense, robustness, and adapt

252 supramolecular assembly with a hybridization architecture that enhances the templated reaction and en

253 enger," may be linked to changes in cellular architecture that favor pathogen-host interactions.

254 ts into S. epidermidis biofilm formation and architecture that improve our understanding of persisten

255 es synergistically configure a catalytic CRL architecture that is both robust, to enable rapid ubiqui

256 Here we use an alternative architecture that realizes a giant atom by coupling smal

257 mology 2 (SH2) domain has a highly conserved architecture that recognizes linear phosphotyrosine moti

258 identifies a perinuclear ncMTOC with unique architecture that regulates microtubules, serving vital

259 uctures with specific micro- and macroscopic architectures that are impossible to achieve through tra

260 d in widespread conserved bicistronic operon architectures that are reminiscent of those typically se

261 T, a new sequence alignment strategy for GPU architectures that is domain independent, supporting ali

262 ictable from the physics of evolution toward architectures that offer greater flow access through the

263 thus stabilizing those cytoskeletal filament architectures that result in shear-like pulling geometri

264 e adapted Arioc to recent multi-GPU hardware architectures that support high-bandwidth peer-to-peer m

265 In the resulting CMGA architecture, the AND-1 trimer is closely positioned to

266 Despite its asymmetric architecture, the gamma-TuRC arranges gamma-tubulins int

267 ity, full-length AcrIIA1 uses its two-domain architecture to act as a "Cas9 sensor," tuning acr expre

268 RICOPILI has a flexible architecture to allow for ongoing development and incorp

269 The proposed device uses a differential architecture to compensate for environmental variations

270 We used a recurrent-neural-network architecture to predict the inclusion of a spliced exon

271 two orthogonal and synergistic deep learning architectures to characterize and optimize toeholds.

272 We investigated two molecular architectures to create agents that detect beta-gal acti

273 Recent advances in adapting deep architectures to structured data have opened a new parad

274 e quiescent state, root and shoot growth and architecture, to flowering and seed production.

275 To evaluate generality, we test our architecture trained only with mosquito images on bumble

276 r unique GRN organization and cis-regulatory architecture underlies this special class of behavior, a

277 n to providing key insights into the genetic architecture underlying normal corneal function, these r

278 of ADHD symptoms into adulthood, the genetic architecture underlying the trajectory of ADHD over time

279 i-manual methods, characterization of z-line architecture using the metrics discussed and implemented

280 Designing 3D printed micro-architectures using electronic materials with well-under

281 udy possible hydrogenation effects on select architectures using in-situ Raman spectroscopy.

282 re, a more complex patterned graphene hybrid architecture was constructed, taking advantage of the si

283 protein critical for the interphase nuclear architecture, was reduced.

284 's implementation to exploit this GPU memory architecture we obtained a further 1.8x-2.9x increase in

285 cell rapidly and completely reorganizes its architecture when it divides is a problem that has fasci

286 We propose a model of sorghum cell wall architecture which is dominated by interactions between

287 ed promoters represents a composite promoter architecture, which can function both coordinately and d

288 ut also on its subcellular (ultrastructural) architecture, which enables cardiac contraction.

289 Pases are key regulators of the cytoskeletal architecture, which impact a broad range of biological p

290 Our architecture, which we call DynaMoE, provides a fundamen

291 indicative of the rareness of tri-aspartate architectures, which allows for engineering such a selec

292 desmosomal cadherins is known, the desmosome architecture-which is essential for mediating numerous f

293 uctures-have been realized through molecular architecture with exceptional control, the design and sy

294 Reserpine induced changes in the sleep architecture with more transitions between states, and a

295 field-effect transistor (FET)/chemiresistor architecture with selective antibodies against Sec-deliv

296 ens promising prospects for new tetrapyrrole architectures with distinct properties and functionaliti

297 c chromeno[3',4':2,3]indolizino[8,7-b]indole architectures, with six fused rings and four contiguous

298 itin ligase subtype and reveal how a defined architecture within a disordered region contributes to E

299 AE enhancement enables deeper discrimination architectures without inhibiting model convergence.

300 o investigate its effect on corneal collagen architecture, x-ray scattering and electron microscopy d