ライフサイエンスコーパス: 3D image

1 g, a time-multiplexing process, to capture a 3D image.

2 ifferent object planes as represented in the 3D image.

3 d area were given based on the reconstructed 3D image.

4 ein structures as if they were multi-channel 3D images.

5 e results of which substantiate the TOF-SIMS 3D images.

6 y in situ, combined with tissue clearing and 3D imaging.

7 E2-dependant engulfment of LCs by real-time 3D imaging.

8 priori knowledge of the target location for 3D imaging.

9 o the artifact issues encountered with gated 3D imaging.

10 ceptible to fetal movement, particularly for 3D imaging.

11 toms and an ex vivo chicken liver through 2D/3D imaging.

12 required in conjunction with high resolution 3D-imaging.

13 ination to enable dynamic three-dimensional (3D) imaging.

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

15 It improves the 3D imaging ability of SPIM in resolving complex structur

16 a simple, open-geometry electromagnet, with 3D image acquisition over the entire brain in 6 minutes.

17 selective arterial spin labeling (VSASL) and 3D image acquisition with whole-placenta coverage.

18 By two-dimensional (2D) and 3D imaging after immunolabeling, both proteins also colo

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

20 We developed quantitative 3D image analysis and clonal analysis tools, which revea

21 For the first time 3D image analysis was carried out by synchrotron radiati

22 Fluorescence-based growth curves, 3D image analysis, immunohistochemistry and treatment re

23 With the increased use of 3D image analysis, standards to ensure the accuracy and

24 In addition to traditional 3D image analysis, we have developed algorithms to opera

25 advantage of volume electron microscopy and 3D image analysis.

26 adhesives in cavities through 3-dimensional (3D) image analysis.

27 ant unilamellar vesicles (GUVs), a dedicated 3D-image analysis, and a quantitative analysis based in

28 A range of high-resolution 3D images and animations can be projected, setting the f

29 e intracellular lipid distribution in 2D and 3D images and can be used to determine the degree of sat

30 MR applications simulate 3D images and reduce the offset between working space an

31 everal major methods for visualizing typical 3D images and related multi-scale, multi-time-point, mul

32 zation histochemistry to produce both 2D and 3D images and to visually align and quantify expression

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

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

35 Here, we use 3D imaging and analysis of dendritic spine morphometry t

36 d for intracellular dye filling, followed by 3D imaging and analysis of dendritic spine morphometry.

37 of 3D SS-OCT permits for the nondestructive 3D imaging and analysis of enamel crack behavior in whol

38 sed single-cell microinjections and advanced 3D imaging and analysis techniques to extend these findi

39 rough finding applications that benefit from 3D imaging and at the same time utilize the unique chemi

40 Integrating these systems with 3D imaging and biochemical assays revealed that ECs incr

41 Here, we use 3D imaging and cellular and clonal analysis, combined wi

42 inal cord, we also assessed CST-YFP mice for 3D imaging and found that YFP fluorescence in CST-YFP mi

43 Using 2D and 3D imaging and image segmentation, we characterized two

44 new pathway towards enabling high-resolution 3D imaging and inspires broader range application of het

45 place within a few hundred fs to ps, using a 3D imaging and laser pump-probe technique.

46 We demonstrate this combined 3D imaging and machine learning method can be used to un

47 We used time-lapse 3D imaging and mathematical modeling to assess root syst

48 This combined approach of 3D imaging and metabolomics provides a new strategy for

49 We used time-lapse 3D imaging and quantitative image analysis to determine

50 al PTM were demonstrated for high-resolution 3D imaging and spectral identification of up to four chr

51 Terahertz scanning reflectometry, terahertz 3D imaging and terahertz time-domain spectroscopy have b

52 combination of comprehensive high resolution 3D imaging and tissue histology to identify abnormalitie

53 ith phase masks is a promising technique for 3D imaging and tracking.

54 nely collect multichannel three-dimensional (3D) images and time series, but analyzing such complex d

55 e pairs within a circadian gene module using 3D imaging, and found periodicity in the movement of clo

56 re using chromosome conformation capture and 3D imaging, and function using RNA-sequencing.

57 le-photon lidar at video rates for practical 3D imaging applications.

58 Using a 3D imaging approach with seedlings grown for various tim

59 Using 3D imaging approaches, we established an integrative blu

60 3D images are derived for different objects with varying

61 Multicoloured holographic 3D images are produced by using angular multiplexing, an

62 Typically, three-dimensional (3D) images are acquired by sequentially capturing a seri

63 Obtaining 3D images at this improved resolution will allow CXDI to

64 imaging with PAT, there is still a need for 3D imaging at centimeter depths in real-time.

65 In gliding motility assays we performed 3D imaging based on fluorescence interference contrast m

66 A 3-dimensional (3D) imaging-based patient-specific dosimetry methodology

67 assessment of potential sources of error in 3D images, both in terms of magnitude and position, espe

68 re distance and construct three-dimensional (3D) images by detecting the time or the phase difference

69 Our simplified approach to 3D imaging can readily be extended to nonvisible waveban

70 The high lateral resolution and 3D imaging capabilities of SIMS combined with the multip

71 ntil recently, technical limitations such as 3D imaging capabilities, computational power and cost pr

72 chnique in the life sciences due to its fast 3D imaging capability of fluorescent samples with low ph

73 The 3D imaging capability of OCT and OCM provided complement

74 sign, high resolution, large depth of field, 3D imaging capability, scalability to shorter wavelength

75 Here we report the development of 3D imaging cluster Time-of-Flight secondary ion mass spe

76 neration and quantitative measurement, (iii) 3D image comparison, fusion and management, (iv) visuali

77 cattering of metal nanoparticles can provide 3D imaging contrast in intact and transparent tissues.

78 Patients studied had both 2D-TEE and 3D imaging (contrast CT and/or 3D-TEE) of the aortic ann

79 In 3D images, contrast medium occupied 39.0% to 52.1% of th

80 Here, we use time-lapse and 3D imaging coupled with computational analysis to map th

81 ed at each particle's position via the local 3D image cross correlation of the two detection channels

82 Our method combines 3D image data acquisition, visualization and on-line ima

83 postprocessing can introduce artifacts into 3D image data and proposes steps to increase both the ac

84 to view arbitrary sections of raw and mapped 3D image data in the context of a web browser.

85 ry to unpack the rich information encoded in 3D image data into a straightforward numerical represent

86 icroscopy (FIB-SEM), can be used to generate 3D image datasets for visualizing and quantifying comple

87 uctures, within our large three-dimensional (3D) image datasets.

88 ment along respiration was extracted using a 3D image deformation algorithm, and this information was

89 High-resolution 3D images demonstrated that vascular amyloid developed i

90 th 2D data analysis, we used edge-preserving 3D image denoising prior to segmentation to reduce stron

91 nd should permit applications in noninvasive 3D imaging (e.g., the lymphatic system).

92 s via simple 2D images without sophisticated 3D-imaging equipment and with better than specialist per

93 r acquisition, visualization and analysis of 3D images for roundworm, fruitfly, dragonfly, mouse, rat

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

95 In light of recent advances in 3D imaging for visualizing axons in unsectioned blocks o

96 achieved cross-talk-free three-dimensional (3D) imaging for four dyes 10 nm apart in emission spectr

97 elective technique generates high-resolution 3D images, from which semi-quantitative information may

98 lved when adding information from CT FFR and 3D image fusion (six of eight, 75%).

99 Software facilitating multimodal 3D image fusion was developed.

100 In silico generated 3D images gathered by micro CT showed pulmonary vasculat

101 nal phenomenon, it is hardly surprising that 3D imaging has had a significant impact on many challeng

102 Three-dimensional (3D) imaging has a significant impact on many challenges

103 Utilizing whole LN 3D imaging, histo-cytometry, and intravital 2-photon mic

104 3D imaging importantly allowed discernment of clusters o

105 ys can project the correct perspectives of a 3D image in many spatial directions simultaneously.

106 asure of facial masculinity/femininity using 3D images in a large sample (n = 1,233) of people of Eur

107 rendering of high-resolution, full-parallax 3D images in a very wide view zone (up to 180 degrees in

108 ves, enabling acquisition of high-resolution 3D images in deep tissue.

109 This preparation enables direct 3D imaging in 500- to 750-nm sections with interferometr

110 l, and DESI-MS imaging can be used for lipid 3D imaging in an automated fashion to reveal heterogenei

111 n imaging, we must address the challenges of 3D imaging in an optically heterogeneous tissue that is

112 in CST-YFP mice is faint for clearing-based 3D imaging in comparison with fluorescence in Thy1-YFP-H

113 g the atomic scale, two-dimensional (2D) and 3D imaging in electron microscopy has become an essentia

114 he multifocus system enables high-resolution 3D imaging in multiple colors with single-molecule sensi

115 low-coherence interferometry for label-free 3D imaging in scattering tissue.

116 motivated development of three-dimensional (3D) imaging in both light and electron microscopies.

117 tive visualisation for grey-level and colour 3D images including multiple image layers and spatial-da

118 dent individually; each reviewed 2D and then 3D images, including color and spectral Doppler.

119 ional fluorescence microscopy--which records 3D image information as a function of time--provides an

120 etic navigation in combination with accurate 3D image integration allowed safe and successful elimina

121 sing magnetic navigation in conjunction with 3D image integration in patients with previous intra-atr

122 vigation-guided ablation with 3-dimensional (3D)-image integration could provide maximum benefit in p

123 e combination of remote magnetic navigation, 3D-image integration, and electroanatomic mapping system

124 model for a shale system for which the full 3D image is available and its properties can be computed

125 Quantitative 3D imaging is becoming an increasingly popular and power

126 situ, the availability of these methods for 3D imaging is expected to provide deeper insights into u

127 Perhaps most important for 3D imaging is that the distance the image plane moves in

128 e of the myocardium, deep three dimensional (3D) imaging is difficult to achieve and structural analy

129 Three-dimensional (3D) imaging is used to demonstrate that once these lipid

130 Here, we review the current state of 3D imaging mass spectrometry as well as provide insights

131 High-quality 3D imaging may be an ultimate solution for revealing the

132 In situ 3D imaging measurements provide unprecedented, quantitat

133 Compared to other 3D imaging methods such as geometry modeling and 3D-scan

134 it to find its own niche alongside existing 3D imaging modalities through finding applications that

135 As such, it provides a novel 3D imaging modality inheriting the advantages of imaging

136 ltislice cross-sectional (three-dimensional [3D]) imaging modality that is characterized by poor soft

137 during the development of serial-sectioning 3D imaging MS and discusses the steps needed to tip it f

138 Serial 3D imaging MS has been steadily developing over the past

139 We demonstrate the feasibility of LAESI 3D imaging MS of metabolites in the leaf tissues of Peac

140 dvantage of the extra spatial dimension that 3D imaging MS offers.

141 Serial 3D imaging MS reconstructs 3D molecular images from seri

142 The future success of 3D imaging MS requires it to find its own niche alongsid

143 3D images (n = 241) were obtained prior to NAM initiatio

144 g can computationally "freeze" the heart for 3D imaging, no previous algorithm has been able to maint

145 ) multidimensional image visualization, (ii) 3D image object generation and quantitative measurement,

146 ogous' images) comprising mixtures of 2D and 3D image objects.

147 denoted as two- or three-dimensional (2D or 3D) image objects of biological interest.

148 to investigate the topology of astrocytes in 3D images obtained by two-photon microscopy of living AP

149 ted from the US data, and a surface-rendered 3D image of the tumor, in relation to the breast surface

150 tructure of the Drosophila brain by browsing 3D images of a brain with subregions displayed as colour

151 The SPECT/CT scans were used to generate 3D images of cumulated activity.

152 We have also started incorporating full 3D images of gene expression that have been generated us

153 We use these experiments to reconstruct 3D images of growing Li dendrites from MRI, revealing de

154 file as output, as well as dynamic movie of 3D images of intermediate conformations during the compu

155 earing, mPAM generates micrometer-resolution 3D images of paraffin- or agarose-embedded whole organs

156 platinum replication creates high-contrast, 3D images of the cytoplasmic surface of the plasma membr

157 The model generates 3D images of the resulting acinar distribution and calcu

158 and delineating nuclear boundaries in 2D and 3D images of varying complexities.

159 Here, we report quantitative 3D imaging of a whole, unstained cell at a resolution of

160 This work hence paves a way for quantitative 3D imaging of a wide range of biological specimens at na

161 pers in this issue move toward this goal via 3D imaging of active neurons across the entire mouse bra

162 emonstrate the application of this method to 3D imaging of bacterial protein distribution and neuron

163 Reconstruction of the TIRF images enabled 3D imaging of biological samples with 20-nm axial resolu

164 n situ hybridization (TEL-FISH) coupled with 3D imaging of buccal cell nuclei], providing high-resolu

165 article we review several methodologies for 3D imaging of cells and show how these technologies are

166 Many biological investigations require 3D imaging of cells or tissues with nanoscale spatial re

167 tudy demonstrates the utility of FIB-SEM for 3D imaging of collagen gels and quantitative analysis of

168 several orders of magnitude that enable the 3D imaging of dilute biomolecules including gases.

169 Here we report 3D imaging of dislocations in materials at atomic resolu

170 tion kinetics, and the surface profiling and 3D imaging of dye sensitized TiO2 films.

171 We developed an image analysis pipeline for 3D imaging of GEMs in the context of large, multinucleat

172 n of substrate and lipid tracers in confocal 3D imaging of individual proteolipobeads.

173 to be compatible with fixation thus allowing 3D imaging of LDs in their cytoplasm environment.

174 nally, TP-alpha was successfully applied for 3D imaging of live islets by staining alpha cell directl

175 LS-RESOLFT nanoscopy offers wide-field 3D imaging of living biological specimens with low light

176 Cryo-electron tomography (cryo-ET) enables 3D imaging of macromolecular structures.

177 Nanometer-scale 3D imaging of materials properties is critical for under

178 The 3D imaging of mature field-grown root crowns showed that

179 We have built an optical lens system for 3D imaging of objects up to 6 mm wide and 3 mm thick wit

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

181 mp-probe spectroscopy permits nondestructive 3D imaging of paintings with molecular and structural co

182 ntrast agent and pH-responsive nanoprobe for 3D imaging of pH distribution.

183 two-dimensional (2D) imaging and three-color 3D imaging of proteins in fixed cells.

184 ible and versatile clearing procedure called 3D imaging of solvent-cleared organs, or 3DISCO, which i

185 e allows fast, high-contrast, and convenient 3D imaging of structures that are hundreds of microns be

186 3D imaging of the bone vasculature is of key importance

187 labeling technologies prohibits quantitative 3D imaging of the entire contents of cells.

188 eliable method of generating high-resolution 3D imaging of the fetal vasculature.

189 easily recognized via surface profiling and 3D imaging of the films.

190 ngiography (OCTA) is a noninvasive method of 3D imaging of the retinal and choroidal circulations.

191 3D X-ray histology allows for nondestructive 3D imaging of tissue microstructure, resolving structura

192 Thus, 3D imaging of whole cells (or even large organelles) sti

193 aring protocol that removes melanin allowing 3D imaging of whole eyes and visual pathways.

194 imaging probe to produce three-dimensional (3D) images of cell surface.

195 Three-dimensional (3D) images of the anterior laminar surface and the perip

196 roviding high-resolution, three-dimensional (3D) imaging of fluorescent molecules.

197 py, as we demonstrated by three-dimensional (3D) imaging of fluorescent pollens and brain slices.

198 d that has enabled successful 3-dimensional (3D) imaging of intact tissues with high-resolution and p

199 we successfully performed three-dimensional (3D) imaging of mammalian nuclei by combining coherent x-

200 Three-dimensional (3D) imaging of molecular distributions offers insight in

201 High-speed, large-scale three-dimensional (3D) imaging of neuronal activity poses a major challenge

202 ctron tomography provides three-dimensional (3D) imaging of noncrystalline and crystalline equilibriu

203 non-destructive tool for three-dimensional (3D) imaging of strain and defects in crystals that are s

204 High-definition and three-dimensional (3D) imaging of the normal retina and optic nerve head we

205 Here we present three-dimensional (3D) imaging of vacuum fluctuations in a high-Q cavity ba

206 equence-based domain pictogram, as well as a 3D-image of the protein structure, and in a molecular gr

207 ble visualization and interpretation, on one 3D image, of the temporal enhancement patterns that occu

208 ve-cell imaging with 2-photon microscopy and 3D imaging, of Wt1-EGFP transgenic mice.

209 Such data presented as 3D images or 3D printed models, will inform discussions

210 Such three-dimensional (3D) images, or holograms, can be seen with the unassiste

211 This high-throughput 3D imaging platform could in general be quite valuable f

212 ded to aid researchers entering the field of 3D image processing of plant cells and tissues and to he

213 l IT neurons in monkeys viewing stereoscopic 3D images projected on a large screen.

214 stimated strain can be insightful to improve 3D imaging protocols, and the computer code of LWM could

215 adiation dose but only a minimal decrease in 3D image quality at all patient sizes.

216 The 3D image quality decreased slightly from a median score

217 lude morphogenesis, we developed an improved 3D image reconstruction approach.

218 This method enables 3D image reconstruction of a crystal volume from a serie

219 netic resonance force microscopy (MRFM) with 3D image reconstruction to achieve magnetic resonance im

220 We used electron cryomicroscopy and 3D image reconstruction to examine the IMNV virion at 8.

221 3D image reconstruction without scatter correction subst

222 Using electron microscopy and 3D image reconstruction, we show that the mutant troponi

223 specimen preparation, low-dose imaging, and 3D image reconstruction.

224 e cryoelectron microscopy three-dimensional (3D) image reconstruction of the A6.2/MNV-1 complex indic

225 Three-dimensional (3D) image reconstruction of tumors based on serial histo

226 hanks to the volume rendering techniques and 3D image reconstructions, it is possible to precisely de

227 of prenatal MRI with novel, motion-corrected 3D image registration software, as an adjunct to fetal e

228 Here we show that 3D images related to LSPRs of an individual silver nanoc

229 However, 3D imaging remains limited to anisotropic resolution and

230 lication of 3DE will rely mainly on improved 3D image resolution and volume rates.

231 fluorophores opens up avenues for improving 3D imaging resolution beyond the Rayleigh diffraction li

232 We also obtained sharp, specific 2D and 3D imaging results for early stage apoptosis in breast c

233 The 3D images reveal the nanomechanical morphology of unfixe

234 Microangiography and 3D imaging revealed patchy perfusion of Egfl7(-/-) place

235 the positional guidance of a SPECT/CT-based 3D imaging roadmap, in this process we studied to which

236 Two observers read the 2D and 3D images separately in a blinded manner for bone and no

237 gles scanning to computationally reconstruct 3D images sequences.

238 e used in CE MR angiography to acquire (a) a 3D image series with 1-second frame time, allowing accur

239 f 3D anisotropic wavelet in classifying both 3D image sets and ROIs.

240 lters which extract textural features in the 3D image sets to build (or learn) statistical models of

241 copy (SIM), we have captured high-resolution 3D images showing MOF uptake by HeLa cells over a 24 h p

242 mber of biological samples generating 2D and 3D images showing molecular localization on a subcellula

243 ing confocal microscopy and high-performance 3D imaging software.

244 ducible high-throughput dense phenotyping of 3D images, specifically geared towards biological use.

245 images to the third dimension, we examined a 3D image stack from serial-section TEM (ssTEM) of the op

246 Given a 3D image stack of the animal and a 3D atlas of target ce

247 nt during a complete yeast cell cycle at one 3D image stack per second reveals an unexpected degree o

248 s ~8 d from isolating the tissue to having a 3D image stack.

249 gmentation (SRS) of cells, and applied it to 3D image stacks of the model organism Caenorhabditis ele

250 -localisation measurements of 3-dimensional (3D) image stacks are biased by noise and cross-overs fro

251 urface generation; an automated pipeline for 3D image stitching; and an automated pipeline for neuron

252 Using a novel, 3D imaging strategy, we visualized live oxytocin-induced

253 n powerful and extremely accurate high-speed 3D imaging systems ubiquitous in nowadays science, indus

254 Three-dimensional (3D) imaging systems capture detailed and accurate measur

255 fully understood and a spectrally sensitive 3D imaging technique is needed to visualize the excitati

256 In this protocol, we describe a 3D imaging technique known as 'volume electron microscop

257 Photometric stereo is a three dimensional (3D) imaging technique that uses multiple 2D images, obta

258 using a novel high-resolution 3-dimensional (3D) imaging technique.

259 The spatial resolution of 3D imaging techniques is often balanced by the achievabl

260 so employed optical coherence tomography and 3D imaging techniques to assess and compare whole or bro

261 X-ray-based 3D-imaging techniques have gained fundamental significan

262 is study, we examined the feasibility of two 3D imaging technologies, optical coherence tomography (O

263 Three-dimensional (3D) imaging technologies are beginning to have significa

264 3D-imaging technologies provide measurements of terrestr

265 Using the same nanometer scale 3D imaging technology on appropriately stained frog neur

266 tical defects were identified better on OSEM-3D images than on FBP images.

267 It was found from the 3D images that the healthy skin samples exhibit regular

268 provements have led to real-time full-volume 3D imaging that is no longer prone to the artifact issue

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

270 ation to model immune-mediated GI damage and 3D imaging to analyze T cell localization, we found that

271 n analysis, cytogenetics, immunocytology and 3D imaging to genetically map and characterize the barle

272 a genomically accurate 22q11.2DS model, and 3D imaging to identify and quantify phenotypes that coul

273 ly associated with tapetal function, we used 3D imaging to quantify geometric and textural features o

274 Here, we perform comparative 3D imaging to understand age-related perturbations of th

275 equirement for performing three-dimensional (3D) imaging using optical microscopes is that they be ca

276 Current TES systems offer a 2D monitor, or 3D image, viewed directly via a stereoendoscope, necessi

277 ssion of the process necessary to generate a 3D image volume.

278 e cells and associated spatial parameters in 3D image volumes collected from intact kidney tissue.

279 Tracking eye gaze on moving 3D images was technically feasible.

280 In particular, 3D imaging was used to identify the carotid bifurcation

281 With pseudodynamic 3D imaging, we derive individual parameters that are cen

282 Using intravital dye labeling and 3D imaging, we discovered that systems-level vascular pa

283 Using 3D imaging, we find that during fetal development the vi

284 ngle cell RNA-sequencing and high resolution 3D imaging, we further demonstrate that organoid culture

285 g platform that incorporates high-resolution 3D imaging, we identify phenotypes at multiple time poin

286 Optimal 3D images were acquired using a Bi3(+) liquid metal ion

287 ers influencing the quality of the HeLa cell 3D images were investigated.

288 z-corrected 3D images were reconstructed that accurately portray the

289 Axial and three-dimensional (3D) images were qualitatively and quantitatively compare

290 sing filtered back projection (FBP) and OSEM-3D, images were reconstructed from data generated by bot

291 e investigated by immunohistochemistry-based 3D imaging, whole-mount fluorescence staining, and real-

292 modulation of a 64-view backlight, producing 3D images with a spatial resolution of 88 pixels per inc

293 mum axial resolution and was used to collect 3D images with scanning angles up to approximately 70 de

294 roscopy (FIB-SEM) can automatically generate 3D images with superior z-axis resolution, yielding data

295 ractor for extracting textural features from 3D images with xy-z resolution disparity.

296 he first demonstration of analyte-responsive 3D imaging with LSFM, highlighting the utility of combin

297 ., Raman, IR, MS, etc., allow acquisition of 3D images, with a linear spectrum per pixel, but new pla

298 ocardial tissue suitable for high resolution 3D imaging, with implications for the study of complex c

299 f each probe, and thus the construction of a 3D image, without scanning the sample.

300 3D imaging yielded better lesion detectability than 2D (