ライフサイエンスコーパス: architecture

1 togenetic tools can discern their functional architecture.

2 s are constrained by an intrinsic functional architecture.

3 represents a distinctive element of protein architecture.

4 r knowledge, a new perspective on chromosome architecture.

5 tly occurring major changes of parasite cell architecture.

6 ights unexpected variation in plastid genome architecture.

7 on, as well as with preservation of neuronal architecture.

8 n, genomic stability, cell cycle and nuclear architecture.

9 g proliferation, differentiation, and tissue architecture.

10 st species-specific differentiation of brain architecture.

11 uroinflammation, and degradation of neuronal architecture.

12 ntal plasticity in shaping organ biomass and architecture.

13 of compositionally graded multilayer (CGML) architecture.

14 me of these insects and studied their domain architecture.

15 that this interaction might affect nucleoid architecture.

16 able building blocks in their supramolecular architecture.

17 hain, a membrane protein with a novel domain architecture.

18 omic context on replication timing to genome architecture.

19 s in parallel using a pneumatic multiplexing architecture.

20 the maintenance of juxtaglomerular apparatus architecture.

21 w class of nanoobjects with an intriguing 3D architecture.

22 t despite changes in the underlying synaptic architecture.

23 apture structural features within the tissue architecture.

24 me direction rather than a split bipolarized architecture.

25 expressing a reporter gene with a unique 5' architecture.

26 ree-dimensional environment mimicking tissue architecture.

27 l phenotypes and properties, and shape tumor architecture.

28 structs reproducibly generate desired tissue architectures.

29 ications regarding these FGN-based bioactive architectures.

30 predictions of these surface-grafted polymer architectures.

31 also for the design of novel supramolecular architectures.

32 : the need to design effective sophisticated architectures.

33 rformance across a broad spectrum of genetic architectures.

34 echniques to study complex multichromophoric architectures.

35 around existing cellular components to form architectures.

36 s multimaterial fibers with complex internal architectures.

37 representing various commonly observed brain architectures.

38 t toward a better understanding of cognitive architectures.

39 om continents to oceans and contain in their architecture a record of their rift history.

40 distributed representation with our HLA-CNN architecture achieves state-of-the-art results in the ma

41 ring of spins via topological nanomechanical architecture affords a promising route towards the reali

42 ural circuits and optimization in structured architectures, allowing us to systematically dissect how

43 ge) and the individual variability in system architecture and change.

44 ulpting embryonic tissues, maintaining organ architecture and controlling cell behavior, including ce

45 tion of several classifier blocks in the ANN architecture and coupling them with both the sensor chip

46 s to comprehensively investigate the genetic architecture and degree of missing heritability for gene

47 le, is an important component of the overall architecture and depth of the root system; however, litt

48 EmMBD2/3 expression disrupts normal cellular architecture and development of E. muelleri.

49 The architecture and dynamics of the FG-network have been re

50 is is starting to be elucidated, however the architecture and dynamics of the replication fork remain

51 gs provide insight into the unique molecular architecture and export mechanism of the Pel apparatus,

52 Our findings identify an architecture and fate of stomata in hornworts that is an

53 ng more than 1,000 genes relevant to cardiac architecture and function.

54 ablishes a clear link between inner membrane architecture and functional decline.

55 S) in Europe differed substantially in their architecture and functioning.

56 r results show that VACV-A6 has a two-domain architecture and functions in both crescent formation an

57 However, the overall architecture and functions of CST and RPA are distinct.

58 y, the effects of HBBP1 removal on chromatin architecture and gene expression closely mimic those of

59 n remodeling complexes control the chromatin architecture and have important roles in gene regulation

60 tures whose mechanical behavior is driven by architecture and material properties.

61 ic p53 is challenging because of its complex architecture and multiple highly flexible regions.

62 gamma-proteobacteria that affects chromosome architecture and of Lsr2 from Mycobacteria, binds A+T-ri

63 of 4HT treatment induced disorganized tissue architecture and p21-associated differentiation in wdSCC

64 emperature cues helps to optimise plant body architecture and physiology.

65 in tomato, including adaptions of the plants architecture and physiology.

66 tment prevented the loss of trabecular micro-architecture and preserved cortical bone parameters.

67 nzymes, important questions remain about the architecture and regulation of the SCF repertoire, inclu

68 ndle is a dynamic structure that changes its architecture and size in response to biochemical and phy

69 omposite can be ascribed to the hierarchical architecture and special physicochemical features, inclu

70 the two states lead to biofilms with altered architecture and structural integrity.

71 The maintenance of a proper nuclear architecture and three-dimensional organization of the g

72 d BBSome subcomplexes to analyze the complex architecture and to investigate the binding of GPCRs and

73 Here, we prove that a class of hierarchical architectures and a broad set of biologically plausible

74 roaches for the design of alternative device architectures and approaches.

75 lled, has made the development of artificial architectures and devices possible.

76 Promoters and enhancers share similar architectures and functions, and the prevailing view is

77 dies of this emerging class of soft material architectures and identifies current technical challenge

78 which imposes restrictions on sensor device architectures and results in added expense, poorer scala

79 We hypothesized that TOGs have distinct architectures and tubulin-binding properties that underl

80 ted that CLas induced changes in the nuclear architecture, and activated programmed cell death, in D.

81 rent functional categories, a complex clonal architecture, and disease evolution over time.

82 e that disruption of the cytoskeleton, nodal architecture, and other components of axon infrastructur

83 ent RNA hybridization networks with a linear architecture, and we implemented them in Escherichia col

84 Antibodies have complex multistranded architectures, and specific modification of natural anti

85 Exceptions to this universal plastid genome architecture are very few and include the dinoflagellate

86 rm floret-shaped constructs, while fibrillar architectures are formed in water.

87 Nanoscale carbon-rich molecular architectures are not only aesthetically appealing but a

88 tor peptides, which shows that NR quaternary architectures are variable.

89 fined helix-sheet-coil and helix-sheet-helix architectures, are Nature-inspired synthetic mimics that

90 ructure reveals that it also shares the same architecture as FZD5 and FZD7 CRDs.

91 with implications in designing all 2D device architecture as the structural phases in 2D materials su

92 A) assembles into polymorphic capsids, whose architecture, assembly, and stability are still being in

93 me 6, potentially representing the chromatin architecture at the histone locus body.

94 vide a better understanding of the cell wall architecture but also is vital for devising optimum chem

95 number of MPB loci, illuminating the genetic architecture, but also provides a new approach to disent

96 e propose that AtLAZY proteins control plant architecture by coupling gravity sensing to the formatio

97 Overexpression of COL12 also affects plant architecture by increasing the number of rosette branche

98 ate Pi deficiency-induced remodeling of root architecture by modulating Fe homeostasis in roots.

99 S-A anchors cells in place and preserves CNS architecture by reducing tissue stiffness.

100 Here, we show that this chromatin architecture can be predicted de novo using epigenetic d

101 n human body, such as three-dimensional (3D) architecture, cell heterogeneity, nutrient gradients and

102 g highly complex asymmetrical multiantennary architectures, chemical and chemoenzymatic synthesis has

103 irst synthetic, ceramic-based scaffold whose architecture closely mimics that of cuttlebone -a struct

104 results in an artificial biohybrid electrode architecture, combining the photophysical features of PS

105 A metal-free photoanode nanojunction architecture, composed of B-doped carbon nitride nanolay

106 This architecture comprises 6 categories of approximately 40

107 on of a new type of solar cell encapsulation architecture comprising a periodic array of step-index w

108 he monocot lineage, understanding its genome architecture could shed light on plant adaptation and ge

109 Plant forms display a wide variety of architectures, depending on the number of lateral branch

110 ke bone and shell have complex, hierarchical architectures designed to control crack propagation and

111 This unique architecture dictates essential aspects of Ca signaling

112 genomes that has essential roles in nuclear architecture, DNA repair and genome stability, and silen

113 deformation mechanism that emerges in these architectures during loading.

114 mics approach to understanding brain network architecture, employing advanced magnetic resonance imag

115 has been unclear how the possession of this architecture enables higher-level cognitive functions, w

116 Our quantum dot device architecture enables multi-qubit algorithms in silicon.

117 ation may provide a method to manipulate the architecture, flavour and nutritional content of potted

118 This architecture for artificial muscles opens the door to ra

119 Here, we develop a flexible architecture for computing damages that integrates clima

120 esponse to cocaine, and suggest a compelling architecture for differentiation and separate parsing of

121 A new device architecture for fast organic transistor memory is devel

122 We propose a neural architecture for feature binding in visual working memor

123 ow significant overlap with the genetic risk architecture for several psychiatric disorders, fueling

124 es with rationally designed compositions and architectures for potential applications in the field of

125 a significant body of work now exists on the architecture, function, and development of mouse central

126 Bacteroidales possess three genetic architectures (GA1-3) of the type VI secretion system (T

127 This battery architecture gradually integrates controlled amounts of

128 The device architecture has potential for realization of the next g

129 sis of such regularity, mutants with altered architecture have been isolated.

130 Recent investigations of rift architecture have suggested that multiphase deformation

131 ture of light in its simplest form, periodic architectures have enabled a panoply of tunable optical

132 high-dimensional quantum codes in a modular architecture, have potential benefits, but need to be ex

133 rse patterns share a common underlying array architecture, having a core unimodal peak of coaligned m

134 w regulatory design features such as network architecture, hierarchical organization, and cis-regulat

135 ient, miniaturized group IV lasers into CMOS architecture holds the key to the realization of fully f

136 This architecture illustrates how Chd1 senses DNA outside the

137 dable macro language, and extensible plug-in architecture, ImageJ enjoys contributions from non-progr

138 l interaction with Fe3 O4 cores, this unique architecture immobilizes the active material and inhibit

139 demonstrated abnormal stratum corneum lipid architecture in AD and IV HEEs, independent of FLG genot

140 nvestigated the underlying microtubule array architecture in light-grown epidermal cells with explici

141 In support, analysis of genomic architecture in mouse intestinal epithelial cells disclo

142 LAP2beta and disorganizes the nuclear lamina architecture in neurons differentiated from FXTAS iPS ce

143 This hampers the investigation of chromatin architecture in rare cell populations.

144 s, demonstrates the conserved role of genome architecture in regulating DNA replication, and identifi

145 igh-resolution techniques to probe molecular architecture in situ and integrate information from dive

146 Finally, we explored the limit of our architecture in terms of bytes per molecule and obtained

147 ases, the SDA structure adopts an unexpected architecture in which a pair of ISD11 subunits form the

148 ayer MXenes and MXene/carbon nanotube hybrid architectures in terms of capacity, rate capability, and

149 al interaction for designing self-assembling architectures in water.

150 A metal-insulator-semiconductor architecture, in which an insulator film serves as a pro

151 disordered proteins, key components in mRNP architectures, in the embryonic function of lsy-6 miRNA.

152 of disease cases represent different genetic architectures, in which disease-associated variants have

153 rane leads to characteristic cortical tissue architecture, including formation of a polarized cortica

154 The nature of these architectures, including their formation, phase changes,

155 channels and nacre-inspired brick-and-mortar architecture into one materials system.

156 e speculate that the superfamily active-site architecture involved in nucleophile positioning prevent

157 3D printing, and indicate that scaffold pore architecture is a critical variable in additively manufa

158 it's concluded that the created interfacial architecture is a typical complex system, where SPR resp

159 The resulting architecture is able to achieve accurate results with re

160 This architecture is called convergence.

161 by altered extracellular matrix and alveolar architecture is destroyed, which leads to decreased lung

162 tion, we show that this stereotypical tissue architecture is established by a pivot-like process betw

163 nd spreading, a fault-tolerant computational architecture is required.

164 Proof-of-concept that FFLUX's architecture is suitable for geometry optimization is ri

165 tubule networks is hampered by their complex architecture, limiting insights into the interplay betwe

166 f DNase I-hypersensitive sites and 3D genome architecture, linking functional variants to gene transc

167 o)metal(II) (PM'; M' = Zn, Pt, Pd) molecular architecture (M-(PM')n-M), wherein high-oscillator-stren

168 mposites creep resistance due to the network architecture made by the TiB whiskers (TiBw), and a decr

169 siderable diversity in their composition and architecture, many basic mechanisms underlying target re

170 idopteran subfamily Heliothinae suggest that architecture may not constrain ecological adaptation in

171 data suggest that instability in the genetic architecture of a subset of genes could lead to widespre

172 e bacterial microcompartments share a common architecture of an enzymatic core encapsulated in a sele

173 and PIP2, especially within the specialized architecture of axons.-Neverisky, D.

174 The genetic architecture of behavioral traits in dogs is of great in

175 , we aimed to gain insights into the genetic architecture of biomarker traits which can reflect healt

176 provide insights into the underlying genetic architecture of cardiac structure and warrant follow-up

177 vides a comprehensive layout for the genetic architecture of common variants for psoriasis.

178 esearchers to explore the underlying genetic architecture of complex phenotypes at an unprecedented l

179 ddress important questions about the genetic architecture of complex traits, such as allele frequency

180 e synaptic proteins, as well as the detailed architecture of dendritic spines, in mouse brain circuit

181 ple environments to characterize the genetic architecture of floral allocation, including its sensiti

182 We found that the genomic architecture of flowering time has been shaped by the mo

183 ditions to enable exploration of the genetic architecture of flowering time.

184 ht into the nature of the underlying genetic architecture of gene regulation.Covariance of gene expre

185 To understand the genetic architecture of how these two organs covary during devel

186 d revision to account for the parallel input architecture of HVC, along with the orthogonal input top

187 ffects on the stable and time-varying neural architecture of inhibition during a period of neurobehav

188 indings provide new insight into the genetic architecture of intelligence.

189 es, mimicking the modular antenna/transducer architecture of natural photosystems, and by metastable

190 ovide insight into the molecular and genetic architecture of neural phenotypes and the neural mechani

191 required to clearly visualize the functional architecture of physiological structures.

192 The three-dimensional architecture of plant canopies imposes complex light dyn

193 source for discovering the genetic basis and architecture of plant natural products.

194 SpnF active site and inferring the catalytic architecture of possible Diels-Alderases.

195 are warranted to delineate the full genetic architecture of rare complex diseases.

196 of these organs through comparisons with the architecture of rhizophore vascularization in Selaginell

197 l, and ultrastructural analyses to probe the architecture of ribbon synapses by perturbing the functi

198 at unravelling the genetic and environmental architecture of severe mental disorders.

199 Understanding the genetic architecture of speciation is a major goal in evolutiona

200 ess, these amyloid structures illuminate the architecture of the amyloid state, including its stabili

201 twork theory allows to elicit the functional architecture of the brain in terms of links (correlation

202 Here, we investigated the clonal architecture of the CD34(+)CD38(-) hematopoietic stem/pr

203 The three-dimensional (3D) architecture of the cell nucleus plays an important role

204 biochemical assays, we define the molecular architecture of the core human CPSF complex, identifying

205 mapping of the vertex model into the Chimera architecture of the D-Wave machine, initiating an approa

206 e of the scramblase nhTMEM16 has defined the architecture of the family, it was unknown how a channel

207 -specific markers.SIGNIFICANCE STATEMENT The architecture of the functional connectome in focal dysto

208 nesis is a complex mechanism, the regulatory architecture of the immune system is likely to include t

209 To further resolve the genetic architecture of the inflammatory bowel diseases ulcerati

210 and highlight the importance of an atypical architecture of the K2 FERM domain in regulating integri

211 ent along actin is unclear as the underlying architecture of the local actin network is often unknown

212 ematical analyses, we examined the hydraulic architecture of the mature leaves of the model species P

213 is revealed, for the first time, the overall architecture of the MCM-MeaB complex, which exhibits a 2

214 itical roles in its ability to rearrange the architecture of the MT cytoskeleton.

215 Due to the molecular architecture of the nanofibers which puts high density o

216 s in this system thus defines the functional architecture of the network.

217 achieve clinical productivity, the chemical architecture of the oligonucleotide needs to be optimize

218 The genetic architecture of the PR interval comprises modulators of

219 Here, we report that the architecture of the secondary root system in flooded ric

220 The structure reveals the molecular architecture of the TFIIH core complex, the detailed str

221 s), respectively, which mediates the dynamic architecture of the transsulfursome and thus enables a g

222 Here, we describe the circuit architecture of the visual system of Drosophila larvae b

223 Integrating data for the genetic architecture of traits from genome-wide association mapp

224 ion contributes significantly to the genetic architecture of TS.

225 el from Chamaesiphon minutus, CmTMEM175, the architecture of which represents a completely different

226 ide a new platform to uncover quintessential architectures of chaos generation and the underlying phy

227 Compared with other architectures of CNN, Recurrent Neural Network, and Rand

228 nergetically degenerate, hierarchical domain architectures of coexisting c/a and a1 /a2 domain struct

229 Here we compared the chromosomal architectures of fetal and adult human erythroblasts and

230 only terminal glycoepitopes but also complex architectures of glycans can influence binding selectivi

231 portunity to investigate the critical neural architectures of musical processing in the brain.

232 tives at the nanoscale assemble into various architectures of nanocrystals in a binary solution syste

233 tically similar, PutAs vary widely in domain architecture, oligomeric state, and quaternary structure

234 transporters are expected to share the same architecture on the basis of sequence homology.

235 monstrates the importance of MXene electrode architecture on the electrochemical performance and can

236 jor innovation in creating ideal maize plant architecture originated from ectopic overexpression of t

237 to obtain ground-based high-throughput plant architecture parameters of sorghum, a tall and densely p

238 i, leading to disruption of nuclear envelope architecture, partial sequestration of factors essential

239 This coupled cellular oscillator architecture permits stable and replicable ensemble resp

240 quantitative analysis of microtubule network architecture phenotypes in fibroblasts.

241 It demonstrates how seed architecture predetermines the pattern of water intake,

242 erate highly intricate closed supramolecular architectures, ranging from self-assembling cages to vir

243 esulting growths that deform the skin tissue architecture regress, irrespective of their size.

244 t, its precise relationship to local circuit architecture remains unclear.

245 ed QuASAR (quantitative analysis of sacculus architecture remodeling), which measures subcellular pep

246 ines is a challenging task given the complex architectures required for the construction of nanosized

247 findings provide a high-resolution chromatin architecture resource for cardiac epigenomic investigati

248 The MacB architecture serves as the blueprint for understanding t

249 n which the AP axis converges on a molecular architecture similar to that of the direct developing he

250 rising Emu-Myc lymphomas to define transgene architecture, somatic mutations, and structural alterati

251 Thus, analyses of gene gain and losses, gene architectures, synteny and other genomic features can no

252 te-modified loop domain (2Me/PSLOOP MBs), an architecture that elicits marginal levels of nonspecific

253 Podocytes exhibit a unique cytoskeletal architecture that is fundamentally linked to their funct

254 eukaryotic promoters indicates their complex architecture that is often composed of numerous function

255 interaction between atoms, and we propose an architecture that might take advantage of this.

256 ral sequences are produced features a neural architecture that readies different movements simultaneo

257 We expect that similar deep learning architectures that allow learning nonlinear patterns can

258 We found that Msps TOGs have distinct architectures that bind either free or polymerized tubul

259 of modern electronics with multiple stacking architectures that increase the complexity of three-dime

260 self-assembly to generate hydrogel-based 3D architectures that resembles the appealing features of t

261 Our results shed light on the network architectures that underlie external task engagement, an

262 -assemble into various chiral supramolecular architectures, thereby regulating the chiral directional

263 nstruction of covalently linked well-defined architectures thereof, e.g. block copolymers, graft copo

264 in semiconductor devices, but in many device architectures they are nanostructured, disordered and bu

265 oside antibiotics and contributes to biofilm architecture through ionic interactions with extracellul

266 rain tissue based on an individual's genetic architecture, thus enabling the functional validation of

267 ymer) is combined with a carefully optimized architecture to satisfy the electrical requirements for

268 assemblies provides access to unprecedented architectures to be used as nanocarriers.

269 our algorithm takes advantage of multilayer architectures to identify useful higher-order representa

270 We design four different deep learning architectures to predict protein torsion angles.

271 We use circuit quantum electrodynamics architectures to study the internal degrees of freedom o

272 Heterogeneity in genetic architecture underlying complex traits and diseases, whi

273 The degree to which genomic architecture varies across space and time is central to

274 A strategy to reach these architectures via direct difunctionalization of abundant

275 electrochemical aptasensor based on sandwich architecture was developed for detection of CT26 Cells.

276 The honeycomb architecture was modified by control of the honeycomb ce

277 Abnormal vascular architecture was observed in the submucosa of the jejunu

278 CF) with an interconnected micro-/mesoporous architecture was prepared and used as a binder-free, low

279 Using an unconventional multilayer architecture, we demonstrate luminescent hyperbolic meta

280 re directly relevant for determining grammar architecture, we present one main objection to the concl

281 These large-scale changes in nuclear architecture were associated with the deposition of acti

282 Building on this foundation, complex architectures were achieved through copolymerizations of

283 e basal layout from which vertebrate pallial architectures were elaborated.

284 and experimentally realise a quantum network architecture, where the nodes are fully connected using

285 findings indicate that GmCLV1A acts on shoot architecture, whereas GmNARK, functions in controlling n

286 f actions, is a hallmark of the actor/critic architecture, whereas the action-value-prediction error

287 o produce a non-domain-swapped transmembrane architecture, which appears to be a hallmark of this cha

288 of the N, S heteroatom doping and unique SHG architecture, which provide a large surface area and eff

289 ell are spatially organized into an activity architecture whose structural and functional characteris

290 onfirm uniform compression of the pi-stacked architecture with no phase change apparent up to 8 GPa.

291 l Network, and Random Forest, the simple CNN architecture with only one convolutional layer performs

292 example of a discrete metallosupramolecular architecture with segregated guest binding in different

293 ies approaching 10% in planar heterojunction architecture with small (<450 meV) energy loss compared

294 Biomimetic architectures with Bouligand-type carbon nanotubes are f

295 pen, crystalline supramolecular coordination architectures with porous facets.

296 molecules is transmitted to a supramolecular architecture, with a sense of directionality.

297 lus subtilis NrnA reveals a dynamic bi-lobal architecture, with the catalytic N-terminal DHH domain l

298 idate how brain diseases change this modular architecture within brain areas.

299 cers and transcription factors form distinct architectures within these lineages in the spinal cord.

300 throughout the genome, but whether the same architecture would be involved in the generalist's adopt