ライフサイエンスコーパス: 3D imaging

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 3D imaging of the bone vasculature is of key importance

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 3D imaging yielded better lesion detectability than 2D (