ライフサイエンスコーパス: tomogram

1 ent gated acquisition of the second-day rest tomogram.

2 ordinates of candidate-macromolecules in the tomogram.

3 nuclear pore complex obtained from a single tomogram.

4 tching known structures to the cryo electron tomogram.

5 sing the Fourier transform of the RVFV MP-12 tomogram.

6 pre-discharge and 30-day abdominal computed tomograms.

7 d the resolution and the interpretability of tomograms.

8 oteins, averaged 70-79 trimers per virion in tomograms.

9 ings were verified in the postimplant serial tomograms.

10 g both perfusion and function from perfusion tomograms.

11 site using cross-sectional film-based linear tomograms.

12 those from oblique radiographs and computed tomograms.

13 iginal digitized tomograms and the deblurred tomograms.

14 g methods for detection of complexes in cell tomograms.

15 step in a visual proteomics analysis of cell tomograms.

16 lassification of complexes inside whole-cell tomograms.

17 aled by visualization and segmentation of 3D tomograms.

18 model fit to a reconstruction from electron tomograms.

19 d layer (LSL) were delineated in 2D sagittal tomograms.

20 occurring protein complexes in cryo electron tomograms.

21 resolution and low signal-to-noise ratio in tomograms.

22 known macromolecular complexes in whole cell tomograms.

23 y unknown protein complexes in cryo electron tomograms.

24 f 9 subvolumes of the adhesin extracted from tomograms.

25 he perinuclear space as seen in the electron tomograms.

26 The resulting tomograms allow us to locate regions of efficient cathod

27 applicability using realistically simulated tomograms, allowing for the inclusion of noise and disto

28 The tomograms also document pH-induced changes affecting the

29 t and width of the mandible on each original tomogram and each deblurred tomogram in triplicate.

30 dges in lower-resolution electron microscopy tomograms and by "mapping" the functional effects of gen

31 The sagittal tomograms and en face reflectance images over a 2-cm(2)

32 The visual interpretations of tomograms and polar maps, vessel stenosis from coronary

33 firmed by visual inspection of electron cryo-tomograms and power spectra of single projection views,

34 AQ algorithm segmented the LV BPs on the BP tomograms and subdivided volumes into 17 subregions.

35 ht and width for both the original digitized tomograms and the deblurred tomograms.

36 Crystal structures, cryoelectron tomograms, and interlayer chemistry were consistent with

37 rdiograms with Doppler, myocardial perfusion tomograms, and treadmill exercise or pharmacological tes

38 ll candidate macromolecules cut out from the tomogram are available for download.

39 Simulated tomograms are then used for assessing the template-free

40 The server accepts tomograms as they are imaged and reconstructed by Cryo-E

41 ayer through electron cryotomography and sub-tomogram averaging of cell stalks.

42 ryo-ET resolution either by some form of sub-tomogram averaging or template matching, respectively pr

43 Here we use cryo-electron tomography and sub-tomogram averaging to derive the intact structure of the

44 otomography and sub-nanometre-resolution sub-tomogram averaging.

45 obtained by cryo-electron tomography and sub-tomogram averaging.

46 -throughput cryo-electron tomography and sub-tomogram averaging.

47 In tomograms, CaMKII holoenzymes can be visualized directly

48 Tomograms can be averaged when display of only the regul

49 The different time frames of tomograms constitute a movie of the object in motion, th

50 Tomograms constructed from fixed, cryosectioned cells re

51 This task becomes challenging when tomograms contain mixtures of unknown complexes extracte

52 A whole cell cryo electron tomogram contains structural information of all its macr

53 tion in electrical conductivity shown in the tomograms correlate well with diesel removal from the sa

54 Recent studies using chest computed tomograms (CTs) in smokers and in the general population

55 a series of 6 to 11 apical echocardiographic tomograms, depending on heart rate, in 11 patients.

56 a bracelet-like ring structure for which 4D tomograms display different modes of motion, such as bre

57 The tomograms distinguish two kinds of glycoprotein spikes [

58 We provided a sequence-specific cryo-ET tomogram fitting of DNA minicircles, registering the seq

59 cross-bridges through the three-dimensional tomogram from their origins on 14.5-nm-spaced shelves al

60 ubcellular features in 120 platelet electron tomograms from these two groups showed statistically sig

61 m 99mTc-sestamibi myocardial perfusion gated tomograms have demonstrated a high degree of accuracy an

62 nsmission Electron Tomography, the resulting tomograms have excellent (de-)focus and alignment proper

63 -0.58 +/- 1.36 mm) compared to the deblurred tomograms (height: -0.58 +/- 1.16 mm; width: 0.37 +/- 0.

64 We present an interpretation of the tomogram in terms of the packing arrangement of Tsr usin

65 on each original tomogram and each deblurred tomogram in triplicate.

66 s for realistically simulating cryo electron tomograms including noise and image distortions due to t

67 Qualitative inspections of the tomograms indicate significant morphological differences

68 Moreover, the tomograms indicated that the fibrils extract lipid from

69 Automated software transformed cinematic tomograms into images demonstrating uniform appearance o

70 ing of macromolecular complexes found within tomograms is known as subtomogram averaging, and this te

71 alization of macromolecules in cryo-electron tomograms is one of the key procedures to unravel struct

72 In IGS, the surgeon may see any angled tomogram of the patient's body, or 3D anatomies beyond t

73 derately imaged by the inverted conductivity tomogram of the reactor.

74 Unaveraged three-dimensional tomograms of "glycol-stiff" sarcomeres show crossbridges

75 Presurgical conventional tomograms of 23 single-implant sites were analyzed retro

76 Images and tomograms of A/Aichi/68 X-31 virions show the generality

77 ients of an ESCRT cargo protein and electron tomograms of Arabidopsis thaliana endosomes to measure c

78 e that is critical for budding and resembles tomograms of authentic virions.

79 We then establish, using X-ray tomograms of both unpressurised and pressurised arteries

80 Reconstructions of electron tomograms of branch junctions show how Arp2/3 complex an

81 Electron tomograms of capsids attached to or undergoing envelopme

82 ly be good enough to allow interpretation of tomograms of cells, organelles, bacteria and viruses in

83 Here, we present a framework for simulating tomograms of cellular environments at high crowding leve

84 g the procedure to phantom data and electron tomograms of cellular samples significantly improved the

85 rom the statistical analysis of cryoelectron tomograms of cristae vesicles isolated from Drosophila f

86 hods it is crucial to realistically simulate tomograms of crowded cellular environments, which can th

87 Tomograms of IFM treated with AMPPNP at 23 degrees C rev

88 Visualized in cryo-electron tomograms of isolated virions, the tegument was seen to

89 Electron micrographic tomograms of isometrically active insect flight muscle,

90 caveolar membrane profiles were revealed in tomograms of native caveolae inside cells.

91 -band, we have used subtomogram averaging of tomograms of rat cardiac muscle in which subtomograms ar

92 his issue, we have scrutinized cryo-electron tomograms of rat hippocampal neurons for the occurrence

93 Tomograms of rigor IFM show double-headed lead and singl

94 Comparison of in situ crossbridges in tomograms of rigor with atomic model of acto-S1, the com

95 the RV capsid protein with the cryoelectron tomograms of RV particles established a low-resolution s

96 Docking an actoS1 atomic model into EM tomograms of swollen rigor fibers identifies in situ for

97 3D electron tomograms of the caveolar coat, labeled using cavin-Mini

98 Single-tilt tomograms of the dyads in rat ventricular myocytes indic

99 Tomograms of the renal parenchyma reconstructed in three

100 s , which are then back-projected to compute tomograms of the sample.

101 By comparing tomograms of wild type and knockout desmosomes, we have

102 chnique that is used to produce 3D pictures (tomograms) of complex objects such as asymmetric viruses

103 present a method to correct aberrations in a tomogram rather than the beam of a broadband optical int

104 e the initial modeling based on the electron tomogram reconstruction may be suboptimal.

105 The quality of the tomograms recorded with the Volta phase plate enabled a

106 alternative methods in full and undersampled tomogram recovery, but with less significant performance

107 The tomograms reveal a complex network of spectrin filaments

108 Such tomograms reveal that the inner membrane self-assembles

109 These tomograms revealed structures within the Golgi cisternae

110 l comparisons of individual particles in the tomograms revealed that a majority of the complexes have

111 Preimplant spiral tomograms revealed that the initial prosthetic trajector

112 osin subfragment 1 atomic structure into the tomogram reveals that 90 degrees target zone bridges sha

113 gned molecular subvolumes extracted from the tomogram reveals that the vast majority of molecules sho

114 agnetic resonance imaging, positron emission tomogram scan and connectivity studies in anesthesia and

115 catheterization (77%), followed by computed tomogram scans (52%), mostly body examinations.

116 ion that included chest radiograph, computed tomogram scans, radionuclide imaging, diagnostic cardiac

117 Cryo-electron tomograms show that tubes span the periplasmic space and

118 A computerized tomogram showed a ring-enhancing hypodense lesion in the

119 Tomograms showed an increased concentration of Ca in bot

120 In addition, the tomograms showed distortions in the apical region.

121 y for 60 degrees samples of 11-13 short-axis tomograms spanning the entire heart, from which regional

122 d severely changed in averaged cryo-electron tomograms, suggesting that NDK5 is crucial for the intac

123 fast (short-duration) transmission computed tomogram (TCT), acquired immediately before or after the

124 lized by crystal structures and cryoelectron tomograms, the critical gp41-interactive region of gp120

125 ET method for localizing objects within cryo-tomograms to beyond the diffraction limit of the light m

126 onents, and use ligand-oriented cryoelectron tomograms to define component mobility in the viral spik

127 study retrospectively analyzed conventional tomograms to estimate the prognostic value of the cross-

128 The tomograms unambiguously reveal the coexistence of the tw

129 showed perfusion defects on the post-stress tomogram underwent gated acquisition of the second-day r

130 ) acquisition technique that collects apical tomograms using a continuously internally rotating trans

131 s at the macula were quantified by analyzing tomograms using ImageJ.

132 The data set of eight tomograms was digitized and the blur reduced with the de

133 e magnetic catheter, guided by a 3D computed tomogram, was successfully navigated to all pulmonary ve

134 From the tomograms, we measured the surface areas of cores and, h

135 From electron tomograms, we provided evidence that nontubular VWF is a

136 The tomograms were compared with a control cohort (n = 60).

137 ular horizontal and vertical long axis gated tomograms were generated for 116 studies chosen on the b

138 The electron beam computed tomograms were interpreted by a cardiologist with no kno

139 The conventional stress and rest tomograms were interpreted first by means of a 14-segmen

140 ferences in visual acuity, optical coherence tomograms were recorded in some patients to visualize ce