ライフサイエンスコーパス: 3D image

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

2 but the tumor volume was extracted from the 3D image.

3 reate and quantitatively study a microscopic 3D image.

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

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

6 ial markers guided only by the reconstructed 3D images.

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

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

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

10 ipped with retractable septa to allow 2D and 3D imaging.

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

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

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

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

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

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

17 (LSO) detector technology and 3-dimensional (3D) image-acquisition protocols.

18 In 3D images, active cross-bridges are usually single myosi

19 canning confocal microscopy produces blurred 3D images after reconstruction of z stack data.

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

21 anatomy of each donor CT scans by fist using 3D images alone, then transverse images alone, and final

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

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

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

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

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

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

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

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

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

31 Mean times needed to interpret 3D images and measure the BPD and femur were 5.53, 4.79,

32 In the tomographic slices, the 2D and 3D images and polar plots were similar.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 cades was the introduction of 3-dimensional (3D) imaging and its evolution from slow and labor-intens

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

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

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

53 3D images are derived for different objects with varying

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

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

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

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

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

59 d photon transport code, in a 3-dimensional (3D) imaging-based absorbed dose calculation for tumor an

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

61 were highly statistically significant, with 3D imaging being superior in all cases.

62 ection therefore opens up the possibility of 3D imaging by optical sectioning.

63 LD 3D imaging can make (82)Rb PET cardiac imaging more affo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 d that permits the analysis and archiving of 3D image data taken over time.

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

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

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

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

84 Three specific 2D and 3D image-display techniques were tested.

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

86 The accuracy of three-dimensional (3D) image extraction and isotropic resampling techniques

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

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

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

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

91 mensions (87%-90% overlap) was compared with 3D images generated from 2D source images with unequal v

92 rst, anatomic fidelity of three-dimensional (3D) images generated from two-dimensional (2D) source im

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

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

95 mediastinoscopy, bronchoscopy, or endoscopy, 3D imaging helped in preprocedural planning.

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

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

98 to recover chemical shift information within 3D images in a 1D inhomogeneous static magnetic field wi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

116 In addition, 3D imaging is extremely useful in the intraoperative and

117 Another benefit of 3D imaging is the realistic and unique comprehensive vie

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

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

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

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

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

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

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

125 s generally applicable to any time-dependent 3D imaging modality.

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

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

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

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

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

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

132 3D images (n = 241) were obtained prior to NAM initiatio

133 ourse was obtained with computed tomography, 3D imaging (NAVX), or intracardiac echocardiography.

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

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

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

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

138 mplete molecular model of the protein into a 3D image of the protein produced by the crystallographic

139 Not only was a 3D image of the tumor in a retinoblastoma mouse model su

140 ing room, the surgeon can dynamically view a 3D image of the tumor within the breast.

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

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

143 tomography (OPT) to produce high-resolution 3D images of both fluorescent and nonfluorescent biologi

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

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

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

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

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

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

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

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

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

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

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

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

156 To facilitate high-throughput 3D imaging of brain gene expression, a new method called

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 3D imaging of the bone vasculature is of key importance

173 o single-detector row CT for multiplanar and 3D imaging of the central airways.

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

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

176 Sixteen patients underwent 3D imaging of the prostate gland with a 3D endorectal pr

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

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

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

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

181 ization approach in which three-dimensional (3D) images of the developing liver vasculature are gener

182 technique for generating three-dimensional (3D) images of the vasculature from spiral computed tomog

183 Three-dimensional (3D) imaging of delicate, moving soft-tissue body parts i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

201 LSO PET detector technology permits fast 3D imaging protocols whereby weight-based emission scan

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

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

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

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

206 A 3D image reconstruction revealed that dynein's head doma

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

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

209 3D image reconstruction without scatter correction subst

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

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

212 bdomains are located in a three-dimensional (3D) image reconstruction from electron micrographs.

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

214 o-electron microscopy and three-dimensional (3D) image reconstruction to 13 A resolution.

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

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

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

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

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

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

221 gles scanning to computationally reconstruct 3D images sequences.

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

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

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

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

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

227 neovascularization after stroke using a new 3D imaging software program.

228 CT data were analyzed with workstation-based 3D imaging software, with a thresholding procedure based

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

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

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

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

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

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

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

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

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

238 A unique phased-array volumetric 3D imaging system developed at the Duke University Cente

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

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

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

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

243 innovative computer-aided three-dimensional (3D) imaging technique.

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

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

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

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

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

249 cardium was imaged by micro-CT, resulting in 3D images that provided volumes and SAs of the individua

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

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

252 specificity and sensitivity for noninvasive 3D imaging through tissues and whole animals.

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

254 o good energy resolution, which is needed in 3D imaging to minimize scatter and random coincidences.

255 In serial transverse sections of the 3D image, TPL intensity maps of the heart showed cardiac

256 For 3D images, transverse images, and transverse in conjunct

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

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

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

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

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

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

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

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

265 ent coefficients of variation for the 2D and 3D images were 13% +/- 15% and 9% +/- 10%, respectively

266 Comparative 2D and 3D images were acquired for 27 oncology patients using a

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

268 all comparisons, differences between 2D and 3D images were highly statistically significant, with 3D

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

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

271 dial samples were scanned with micro-CT, and 3D images were reconstructed with 21-microm cubic voxels

272 2D CT angiographic sections were quantified; 3D images were reconstructed.

273 udy, circumferential profiles for the 2D and 3D images were similar.

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

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

276 arget-to-background ratio between the 2D and 3D images, when they were filtered with 6-mm and 5-mm ga

277 e image quality of the multi-detector row CT 3D images, while blinded to specific tube currents.

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

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

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

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

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

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

284 dvantages of low cost, portability, and live 3D imaging without offline reconstruction.

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

286 3D imaging yielded better lesion detectability than 2D (