ライフサイエンスコーパス: 3D

1 3D analysis revealed cytoplasmic membranes directly adja

2 3D integration of graphene has attracted attention for r

3 3D laparoscopic display technique optimizes surgical per

4 3D local resolution density map evaluates the three-dime

5 3D models combined with dynamic culture techniques show

6 3D printing (3DP) has transformed engineering, manufactu

7 3D printing has become one of the most promising methods

8 3D printing proved to be a suitable and fast method for

9 3D printing technology has become a mature manufacturing

10 3D printing was used to develop an open access device ca

11 3D-SMART represents a critical step towards the untether

12 training effectively reduced the lag by >=0.3D in individuals of both groups with SVCL and MFCL wear

13 woven textiles or on optimally configured 2D/3D structures such as serpentines and helical coils of c

14 ommon Non-Cartesian readout trajectories (2D/3D radials and spirals), demonstrating efficient anti-al

15 ere, we present a large-scale dataset of 849 3D reconstructions of the basal arbor of pyramidal neuro

16 A 3D model of MpBgl3 was generated by molecular modeling a

17 corded IR images of the subject's breasts, a 3D scanner recorded surface geometries, and standard dia

18 ty spectrometry is implemented by coupling a 3D-printed drift tube ion mobility spectrometer, operate

19 The algorithm tracks whiskers, by fitting a 3D Bezier curve to the basal section of each target whis

20 d for invadopodia activity and invasion in a 3D collagen matrix.

21 ic field to perform different movements in a 3D fluidic environment.

22 hod to measure endothelial permeability in a 3D hydrogel-based vascular model was developed that repl

23 stabilization to the channel, resulting in a 3D reconstruction at 1.9 angstrom resolution.

24 e epithelium and vasculature, we introduce a 3D microfluidic platform that juxtaposes a human mammary

25 This clathrate consists of a 3D Zn-Sb framework hosting K(+) ions inside polyhedral c

26 In the moss, Physcomitrella patens, a 3D leafy gametophore originates from filamentous cells t

27 We performed a 3D movement analysis of runners in order to quantify the

28 pairwise contacts alone to predict absolute 3D positions.

29 will erode at a different velocity, accurate 3D-analysis will require means to establish a spatially

30 o provide an effective approach to achieving 3D sub-diffraction-limit information in subcellular stru

31 ctrolyte is directly visualized via advanced 3D chemical analysis.

32 the first pharmaceutical strongly affecting 3D genome organization.

33 nisotropic nanoparticles into complex 2D and 3D assemblies is one of the most promising strategies to

34 xperiments with murine xenografts and 2D and 3D co-cultures of NHFs and PDAC cells revealed that olde

35 of tumor cells in different in vitro 2D and 3D co-cultures.

36 efficacy of ICT12035, in a number of 2D and 3D proliferation and invasion in vitro assays and an in

37 o-caps can be exploited to build 1D, 2D, and 3D inorganic frameworks.

38 other redox regulatory genes in both 2D- and 3D-culture systems, uncovering a vulnerability of sphero

39 integrates transcription factor binding and 3D genome structure to reflect "transcriptional niche" i

40 tamate sensors combined with patch-clamp and 3D molecular localization reveal that LTP induction thus

41 Using cholangiocyte culture and 3D cholangiocyte spheroid cultures, we found that biliat

42 ing fully three-dimensional displacement and 3D surface tractions at high spatial frequency from epif

43 d fine-resolution diploid chromatin maps and 3D structures and provided insights into the allelic chr

44 tagging, immunofluorescence microscopy, and 3D-structured illumination super-resolution microscopy,

45 HSV-1 infected 2D (neuronal monolayers) and 3D neuronal cultures (brain organoids).

46 y, as observed by ligand preorganization and 3D shape complementarity for the binding pocket.

47 ies, bridging the gap between scientists and 3D printing technology.

48 at a cost of $1,500 using off-the-shelf and 3D-printable parts as an alternative to commercial devic

49 of additive manufacturing, known commonly as 3D printing, this technology has revolutionized the biof

50 e use of an automatic slide loader automates 3D imaging for high sample-throughput.

51 msec) and with a self-navigated "Koosh ball" 3D UTE sequence at free breathing (TE, 0.03 msec).

52 owing to the limitations of extrusion-based 3D printing techniques.

53 Recent advances in image-based 3D genomics techniques have enabled direct tracing of ch

54 pment of biomaterials suited for light-based 3D printing modalities with an emphasis on bioprinting a

55 Together with video-based 3D head-tracking, these results demonstrate endogenous e

56 hich can be used as coating, but can also be 3D printed.

57 low (data acquisition and analysis) for both 3D and 4D-LC/MS setups can be completed within less than

58 monstrate that this method is suited to both 3D structure determination and correlative light/electro

59 ow swarm evolution is strongly controlled by 3D variations in fault architecture.

60 r generating human tissue is demonstrated by 3D bioprinting human airways composed of regionally spec

61 customized scaffolds and surgical guides by 3D printing.

62 ised device was designed for each patient by 3D printing shape of a prism and a hollow base, taking i

63 e new swabs for immediate mass production by 3D printing.

64 d at developing next-generation cellularized 3D scaffolds to mimic anatomical size, tissue architectu

65 no specialized equipment except a commercial 3D printer.

66 h localized control of chromatin compaction, 3D genome organization and the epigenetic landscape.

67 the contact matrix, determining the complete 3D organization of the whole chromatin polymer is an inv

68 ts at the single-cell level within a complex 3D cell environment in a fully automated HTS workflow.

69 n of total axon content in large and complex 3D structures after registration to a standard reference

70 This asymmetry resulted from complex 3D spirals and vaginal folds with deep recesses, which m

71 ere additionally employed to produce complex 3D structures using high-resolution visible light 3D pri

72 These complex 3D axon morphologies drive previously reported 2D trends

73 uctures emerges as a result of the concerted 3D co-assembly of the organic and inorganic components.

74 ults highlight the importance of considering 3D cultures to model host-pathogen interaction.IMPORTANC

75 pe variation analysis, and also to construct 3D protein models for 2b and 3a genotypes.

76 that promote robust formation and controlled 3D organization of microvascular networks.

77 Our method first converts 3D images to key-value data (K-V).

78 most promising methods to construct delicate 3D structures.

79 Designing 3D printed micro-architectures using electronic material

80 -layer assembly of biomaterials in a desired 3D pattern.

81 We show the first detailed 3D terrestrial laser scanning (TLS) estimates of the vol

82 Here, we develop 3D printed bionic corals capable of growing microalgae w

83 prospective study implemented 3-dimensional (3D) isotropic contrast-enhanced T2 fluid-attenuated inve

84 EEC) grown as monolayers or a 3-dimensional (3D) model.

85 vestigated differences in the 3-dimensional (3D) pressure profile of the LES and hiatal contraction b

86 regions while maintaining the 3-dimensional (3D) structure in the murine PDL.

87 g-C(3)N(4) interconnected three dimensional (3D) network of g-C(3)N(4) and GNF.

88 Markedly, achieving three dimensional (3D) rolling rotation of single cells within a larger gro

89 wo types of CNN, one with three-dimensional (3D) and the other with two-dimensional (2D) convolutiona

90 s do not recapitulate the three-dimensional (3D) architecture of brain tissue.We employed human induc

91 cellular tractions within three-dimensional (3D) biomaterials could elucidate collective disseminatio

92 e in the nascent field of three-dimensional (3D) bioprinting.

93 Dispersing RGO on three-dimensional (3D) carbon paper electrodes is one strategy towards over

94 ed an inducible system of three-dimensional (3D) collective invasion to study the behavior and import

95 two-dimensional (2D) and three-dimensional (3D) crystalline arrays.

96 he results suggest that a three-dimensional (3D) crystallographic registry within cage-like superstru

97 Three-dimensional (3D) culture systems have fueled hopes to bring about the

98 SCs (hMSCs) for 96 h on a three-dimensional (3D) ECM-based microgel platform.

99 tated by the evolution of three-dimensional (3D) growth, enabled the generation of morphological dive

100 their demonstration in 2D/three-dimensional (3D) hierarchical film structures broke new ground toward

101 Three-dimensional (3D) hydrogel printing enables production of volumetric a

102 s during the buildup of a three-dimensional (3D) metallic state that follows charge photodoping.

103 diodes (PeLEDs) based on three-dimensional (3D) polycrystalline perovskites suffer from ion migratio

104 Their three-dimensional (3D) position can be resolved by holographic analysis of

105 Three-dimensional (3D) printed prostate cancer models are an emerging adjun

106 Three-dimensional (3D) representations of the environment are often critica

107 ical trial was to compare three-dimensional (3D) ridge changes after immediate implant placement with

108 Three-dimensional (3D) shape perception is one of the most important functi

109 ntoxic measurement of the three-dimensional (3D) spatial distribution of viscoelastic properties with

110 Atomic-level three-dimensional (3D) structure data for biological macromolecules often p

111 sual systems estimate the three-dimensional (3D) structure of scenes from information in two-dimensio

112 cently made to obtain the three-dimensional (3D) structure of the genome with the goal of understandi

113 simulations to determine three-dimensional (3D) structures of activated beta-arrestin2 stabilized by

114 cks to realize deployable three-dimensional (3D) structures of arbitrary shape.

115 M), we resolved the first three-dimensional (3D) structures of K63 ubiquitinated ribosomes from oxida

116 ompared with those from a three-dimensional (3D) U-Net and a coarse-to-fine deep learning method.

117 A generic three-dimensional (3D) U-Net was trained on four different databases to gen

118 Three-dimensionally (3D) printed bioceramic (BioCer) implants consisting of a

119 We also demonstrated the utility of directly 3D-bioprinting and rapidly prototyping of PDMS-based mic

120 dimensional magnetic resonance elastography (3D-MRE), with shear stiffness measured at 60 Hz, damping

121 kerless motion capture system for estimating 3D pose in freely moving macaques in large unconstrained

122 We fabricated 3D-hierarchical sensor interfaces composed of inter-conn

123 We present the first 3D fully kinetic simulations of laser driven sheath-base

124 Five 3D antibody structures associated with the SARS-CoV spik

125 ng models of both measurements (bilinear for 3D images and trilinear for 4D images).

126 for structure determination of COF-300 from 3D-ED data.

127 precision (92.1%), and accuracy (98.4%) from 3D whole-body MRI datasets (field of view coverage, 450

128 arsely-distributed features may benefit from 3D-reconstruction.

129 sensing area, extending data collection from 3D to 4D by tracking real-time biomolecular binding even

130 sions are currently determined manually from 3D CT images by medical experts to avoid damaging the ma

131 growth mechanism of layered perovskites from 3D-like perovskites which can be a general design rule t

132 tissues in these PDMS devices produced from 3D printed molds and after proper device washing and con

133 In this work, we present a fully 3D-printed module for attenuated total reflection Fourie

134 Indeed, functional 3D printable materials can modify their surfaces, struct

135 human skeletal muscle spheroids to generate 3D cortico-motor assembloids.

136 ns, we use nanographenes in SMLM to generate 3D super-resolution images of silica nanocracks.

137 To achieve this goal, 3D MSC sheets are prepared, exploiting spontaneous post-

138 We report a method called 'tomography-guided 3D reconstruction of subcellular structures' (TYGRESS) t

139 Mechanically guided, 3D assembly has attracted broad interests, owing to its

140 headsets are capable to provide holographic 3D guidance to assist CT-guided targeting.

141 Here, we describe how 3D particle sorting can enrich targets at ultralow conce

142 w strategy to incorporate T cells into human 3D skin constructs (HSCs), which enabled us to closely m

143 Due to complexities associated with imaging 3D distribution functions during fast spacecraft motion,

144 ICR mass spectrometry, immunohistochemistry, 3D confocal microscopy, and flow cytometry were used to

145 , and these pairwise couplings have improved 3D structure predictions.

146 In 3D, a substantially larger number of small plaques were

147 nd reconstruct the cranium of M. bassanii in 3D using the rendered models of the elements.

148 ately represents radially symmetric cells in 3D even if cell diameter varies and regardless of whethe

149 ls and patient-derived GBM cells cultured in 3D microwells were co-treated with BAY 11-7082 and TMZ o

150 we parcellated the entire brain directly in 3D, labeling every voxel with a brain structure spanning

151 d adipose tissue segmentation is feasible in 3D whole-body MRI datasets and is generalizable to diffe

152 le, fluid-filled central lumen when grown in 3D matrices.

153 re upregulated in cancer cells maintained in 3D (P < 0.001), cadherin-11 was downregulated (P < 0.001

154 when breast cancer cells were maintained in 3D under fluid flow and pressure.

155 dated through in vitro spray measurements in 3D-printed anatomic replicas using the gamma scintigraph

156 simulations against in vitro measurements in 3D-printed phantoms representing the patient's vasculatu

157 een developed for generating nanoporosity in 3D materials and demonstrate their adaptation for 2D mat

158 n of a coupled single-photon source (SPS) in 3D space via an external magnetic field.

159 Analysis of the inferred 3D-structures indicates no difference in affinity of TDF

160 erritin nodes that predictably assemble into 3D lattices upon coordination of various metal ions and

161 mising approach to transform flat films into 3D complex structures that are difficult to achieve by c

162 In this Feature, we introduce 3D printing as a tool for use in research laboratories,

163 ugh the gold standard for diagnosis involves 3D imaging, 2D imaging by fundus photography is usually

164 Time-lapse 3D confocal microscopy showed that self-lysis occurs loc

165 The high-resolution time-lapse 3D images allow monitoring the progress of reaction fron

166 grated system that combines direct mask-less 3D printed strain gauges, flexible piezoelectric energy

167 ructures using high-resolution visible light 3D printing, demonstrating the broad utility of these ca

168 ovides a new degree of freedom to manipulate 3D graphene electrical properties, which may pave a new

169 cal modelling, additive layer manufacturing (3D printing) and experimental testing are implemented to

170 constriction with pupil diameter and measure 3D blood flow at 99 volumes/second.

171 roscopy (cryo-EM) reconstruction of multiple 3D DNA origami objects.

172 isualizing the large-scale tissue and native 3D organ structure due to its sampling limitation and sh

173 ties, which may pave a new way to design new 3D graphene devices with preserved 2D electronic propert

174 ed to investigate the diagnostic accuracy of 3D imaging of OCT for proximal caries in posterior teeth

175 The accuracy of 3D phasor tracking was extensively tested and compared t

176 as well as molecular mechanisms of action of 3D genome-disrupting drugs.

177 High-throughput analysis of 3D cultures enabled by this TTA has great potential to f

178 a platform for investigating the behavior of 3D tissue models (regardless of biofabrication method),

179 hts the remarkable self-assembly capacity of 3D cultures to form functional circuits that could be us

180 us materials serve as an intriguing class of 3D materials to meet the growing demands for flexible, f

181 the preparation of representative classes of 3D-inorganic nanofiber network (FN) films by a blow-spin

182 pecific DNA targets through a combination of 3D and 1D diffusion mechanisms, with the 1D search invol

183 Here, we present the convergence of 3D printed and paper formats into hybrid devices that ov

184 sents for the first time a rapid creation of 3D scaffolds using magnetic levitation of calcium phosph

185 rocesses as well as recent demonstrations of 3D MEAs to monitor electromechanical behaviors of cardio

186 In this perspective, the development of 3D printable materials with intrinsic functionalities, t

187 current challenges and future directions of 3D MEAs are provided to conclude the review.

188 The DSC of 3D CNN segmentation was comparable among different vendo

189 lic NPs (~3 nm) due to confinement effect of 3D porous structure.

190 el based on detailed manual crown mapping of 3D tree structure.

191 rials enhanced the analytical performance of 3D-printed sample pretreatment devices.

192 fer critical insights into the processing of 3D space in the mammalian brain.

193 The luminance overshoot ratio of 3D/2D hybrid PeLED is only 7.4% which is greatly lower t

194 Capturing the dynamic response of 3D printed phantoms, ex vivo biological tissue, and in v

195 esults provide new insights into the role of 3D niche biomechanics in regulating SC fate choice.

196 nly 7.4% which is greatly lower than that of 3D PeLED (150.4%).

197 provided both comprehensive visualization of 3D spatial relationships and novel means to perform VSP

198 mimetic structure that are entirely based on 3D bioprinting is still challenging primarily due to the

199 impact of DNA damage response and repair on 3D genome folding using Hi-C experiments on wild type ce

200 One 3D print with PLA resulted in an aerosol mass size distr

201 ly heterogeneous aggregates ('organoids') or 3D structures with less physiological relevance ('sphero

202 proaches attempted to engineer solid organs, 3D bioprinting offers unmatched potential.

203 ompeting structures, base triplets, or other 3D non-antiparallel interactions.

204 physostigmine determination with Cu-SWCNT-Pc 3D/GCE were found to be 53 and 177 nM in the range of 0.

205 tforms are potentially capable of performing 3D cell model analysis and cell-therapeutic response stu

206 ile its concave well array hold and perfused 3D-cell constructs.

207 e FDM prostate models are the most preferred 3D printing method by surgeons.

208 -on-a-chip-like platforms along with printed 3D-cell structures.

209 pen-source computational pipeline to produce 3D consistent histology reconstructions of the human bra

210 unds of sequencing are sufficient to produce 3D maps of 36 genomic targets across six chromosomes in

211 A proper 3D/4D image fusion needs to take into account the differ

212 icate the presence of a mechanism to protect 3D genome structure integrity during DNA damage repair.

213 ssion X-ray microscopy, for the quantitative 3D analysis of the evolution of intermetallic precipitat

214 We first review various forms of recent 3D MEAs for in vitro studies in context of their geometr

215 er algorithm that automatically reconstructs 3D whisker information directly from the 'stereo' video

216 ISH imaging offers possibilities for refined 3D reconstruction accuracy evaluation, availability of s

217 ed a new software that can convert a regular 3D scatterplot or network figure to a pair of stereo ima

218 Thus, we report 3D-printed labware designed to measure and handle solids

219 and et al. perform the first high-resolution 3D genome mapping via ChIA-PET to capture RNAPII-associa

220 We established a high-resolution 3D model of molecular marked whole laryngeal cancer by o

221 Here, high-resolution, 3D synchrotron X-ray nano-holotomography images of white

222 The rGO@3D-Cu symmetric cells and half-cells achieve state-of-th

223 Among all the global alignment tools for RNA 3D structures, STAR3D has become a valuable tool for its

224 ales was investigated using two digital rock 3D models, which represented nanoporous organic/mineral

225 rements on fully and semiautomated segmented 3D MRI models to assess glenohumeral anatomy, glenoid bo

226 BC trapping, we employ two parallel sidewall 3D electrodes to produce a dielectrophoretic force which

227 metry and internal architecture has situated 3D printing as an attractive fabrication technique for s

228 raph interpretability and allows us to solve 3D single particle structures of clustered protocadherin

229 tructural characterization with high spatial 3D resolution.

230 to directly measure the orientation spectra (3D orientation plus "wobble") of lipophilic probes trans

231 rformed with a prototypical stack-of-spirals 3D UTE sequence during single breath holds (echo time [T

232 m in mice to determine the epigenetic state, 3D genome architecture and transcriptional landscape of

233 ture solution achieved from room-temperature 3D-ED data with a resolution as low as ca. 3.78 angstrom

234 Photothermal stimulation using NW-templated 3D fuzzy graphene (NT-3DFG) is flexible due to its broad

235 The results indicate that 3D printed MALDI targets are comparable to standard MBT

236 Here, we show that 3D head-orienting movements (HOMs) modulate primary visu

237 in their metastatic potential, we show that 3D refractive index tomograms can capture subtle morphol

238 Together, our results suggest that 3D epigenome remodelling is a key mechanism underlying e

239 The 3D bioprinting of cells, tissues, and organs Collection

240 The 3D CNN identified patients with a large scar burden (>15

241 The 3D microfluidic device is a photoactive polyacrylamide g

242 The 3D printed MALDI targets were validated by analysis of d

243 The 3D-pressure profile of the EGJ at end-expiration and for

244 The 3D-printed conducting polymers can also be converted int

245 The 3D-printed sensor presented here is not only successful

246 Here, we adapted the 3D-bioprinting technology to develop multiple all-inclus

247 Based on both applications, the 3D-printed rGO-PLA showed to be an excellent platform fo

248 i-C datasets, and release the results at the 3D Genome Browser.

249 titatively studying the relation between the 3D fibrillar network and the optical and mechanical prop

250 different sampling sizes is measured by the 3D roughness parameter with [Formula: see text].

251 on qualities which were characterized by the 3D X-ray Computed Tomography (CT) scan and used to train

252 tionship among the paints' compositions, the 3D morphological properties and degradation.

253 rom the single-layer materials, but from the 3D perovskites as well.

254 uence data alone but requires harnessing the 3D structural properties of AAV capsids.

255 ics simulations are employed to identify the 3D nature of an atomic-scale ordering of liquid Ga in co

256 he electrical conductivities achieved in the 3D LM composite are among the state-of-the-art in stretc

257 the key factors for the drug efficacy in the 3D tumor model, governed by the Cu(+2)/Cu(+1) redox pote

258 n be tracked by fluorescence microscopy, the 3D configuration of proteins and lipids at intermediate

259 odels: the 2D Ising ferromagnetic model, the 3D Vicsek flocking model and a small-world neuronal netw

260 point to point mirroring and merging of the 3D created volumes, a method with previous proven high p

261 snapshot of our current understanding of the 3D genome alterations associated with cancers.

262 We discuss potential connections of the 3D genome and cancer transcriptional addiction phenomeno

263 ild replication stress in the context of the 3D genome organization.

264 Reconstruction of the 3D nucleus revealed that distances of the homologous chr

265 oice-related activity, the robustness of the 3D representations further increased for those neurons.

266 The accurate and reliable prediction of the 3D structures of proteins and their assemblies remains d

267 utaraldehyde (GA) on the amino groups of the 3D-Au-PAMAM-p-ABA-SPCE, where tau protein was sandwiched

268 Bone mesenchymal stem cells (BMSCs) on the 3D nanofiber assemblies with smaller pore size show sign

269 integrals of 12.1-37.9 meV rationalizing the 3D electron transport, and relatively high mu(e) of 10(-

270 However, we have shown that the 3D reconstruction method using Focused Ion Beam/Scanning

271 We find that the 3D-3D topotactic transformation involves two types of bu

272 and deep learning to continuously track the 3D kinematics of a rat's head, trunk, and limbs for week

273 We therefore used the 3D genome information along with an ensemble pMHC-I codi

274 are allowed robust quantification, while the 3D properties allowed visualization of the complex confi

275 ue-relevant only if the cells maintain their 3D tissue state during the multi-hour CRRC procedure.

276 ht generation and for stabilisation of their 3D counterparts.

277 Knowledge of their 3D structures is critical to understanding mechanisms of

278 These 3D cell sheets' initial thickness and cellular densities

279 ies with high active volume fraction, thick, 3D-structured electrodes (V(2) O(5) cathode and Li metal

280 This 3D organoid model recapitulates characteristics of BBB d

281 This 3D printed device provides a unique high-throughput in v

282 using aspheric microlenses generated through 3D-microprinting.

283 rom efficient, high-performance displays, to 3D imaging and all-organic spintronic devices.

284 rug-target interactions without resorting to 3D modeling.

285 connected ribbons provide scalable routes to 3D surfaces with a broad range of targeted shapes.

286 ) microscopy and its two-dimensional (2D)-to-3D transformation algorithm to provide an effective appr

287 bi-functional PEDOT interface with a tunable 3D nanofibrous network and carboxylic acid groups (i.e.

288 lity, low numerical dispersion, unstructured 3D gridding, and discrete fraction modeling.

289 Using 3D cell culture, it is shown that drug release is commen

290 A shift in emphasis from using 3D printing for prototyping, to mimic conventionally man

291 Here, using 3D straining in nanocomposite films of (SmMnO(3))(0.5)((

292 l in terms of translation and rotation using 3D reconstruction, point to point mirroring and merging

293 generating large bone defects in sheep using 3D-printed customized calcium phosphate scaffolds with o

294 for generating functional human tissue using 3D bioprinting.

295 to further accelerate innovations in various 3D culture applications such as high-throughput/content

296 f 17] and specificity of 94% [222 of 237] vs 3D CNN, sensitivity of 76% [13 of 17] and specificity of

297 With 3D Magnetic Resonance (MR) Spirometry, local ventilation

298 ynergistic integration of nanomaterials with 3D printing technologies can enable the creation of arch

299 hundreds of picolitre-sized droplets within 3D-printed, multi-layer networks.

300 in which tumor spheroids are embedded within 3D collagen matrices with well-defined IFs.