ライフサイエンスコーパス: micrograph

1 recording optical voltammograms in a single micrograph.

2 document it with drawings and light and SEM micrographs.

3 tion of the leaves and to light and electron micrographs.

4 ormed unbiased disector counts from electron micrographs.

5 es with low detergent background in electron micrographs.

6 n relative chloroplast volume estimated from micrographs.

7 and reconstructed in 3D from serial electron micrographs.

8 on the spiral anode is clearly shown in SEM micrographs.

9 reconstructions from serial-section electron micrographs.

10 oscopic localization of proteins in electron micrographs.

11 known 3D structures, in single electron cryo-micrographs.

12 ynaptic dense projection protein in electron micrographs.

13 usly estimated from the analysis of electron micrographs.

14 dendrites reconstructed from serial electron micrographs.

15 rings when reconstructed from cryo-electron micrographs.

16 ming findings that we obtained from electron micrographs.

17 xhibited thicker fibers in scanning electron micrographs.

18 was observed in nemaline muscle in electron micrographs.

19 ed resolution is comparable to that of still micrographs.

20 ion for the small ECS visualized in electron micrographs.

21 ne aggregates of protein and DNA in electron micrographs.

22 tween immunogold particles in immunoelectron micrographs.

23 cles that have a suitable orientation on the micrographs.

24 ional area was measured in low-magnification micrographs.

25 ally arranged troponin complexes in electron micrographs.

26 ng outer spore coat in thin-section electron micrographs.

27 ty were determined in the high-magnification micrographs.

28 om cryo-negative stain transmission electron micrographs.

29 ssment, sorting and hole masking of electron micrographs.

30 recognition of particle images from cryo-EM micrographs.

31 ayer were reconstructed from serial electron micrographs.

32 lowed us to identify this morphotype in STEM micrographs.

33 measured by direct counts of tiled confocal micrographs.

34 ubunit mapping onto 2-D images from electron micrographs.

35 itting an equation to widefield fluorescence micrographs.

36 e beads was measured using image analysis of micrographs.

37 ndependently of their appearance in electron micrographs.

38 ilic precipitate that is visible in electron micrographs.

39 y single-particle reconstruction of electron micrographs a low-resolution, 3D structure of S. cerevis

40 On electron micrographs an average filament length of approximately

41 Cryoelectron micrograph analyses and 3D reconstructions showed that t

42 idual) between particle images on the second micrograph and map projections is determined for all pos

43 results, negative-stain electron microscopy micrographs and a crystal structure of the Anbu particle

44 Electron micrographs and biochemical data with a PFKL/PFKP chimer

45 uscle cells (SMCs) were observed in electron micrographs and by confocal microscopy.

46 system is designed to accept submissions of micrographs and descriptions from any type of tissue (e.

47 c methods were used to analyze the resultant micrographs and determine the age-related changes of the

48 Optical micrographs and fluorescence analysis show the successfu

49 automatically traces nerve fibers in corneal micrographs and generates measures based on these traces

50 Electron micrographs and immunofluorescence staining of rat CB se

51 Electron micrographs and quantitative measurements show that glyc

52 seeds supported results of scanning electron micrographs and quantitatively showed depletion of secon

53 omimetic was characterized with fluorescence micrographs and temperature-dependent fluorescence recov

54 ortions from two-photon excited fluorescence micrographs and through data simulations was found to ex

55 positive puncta, larger profiles in electron micrographs, and more release sites per profile.

56 s of a dimer, appears as a dimer in electron micrographs, and moves processively on actin filaments.

57 However, conventional electron micrographs are simply two-dimensional projections of th

58 Helical 3D reconstruction from electron micrographs at 20 A resolution provides a structure of f

59 As observed in cryo-electron micrographs, AVP-p treatment causes morphological change

60 analysis by image reconstruction of electron micrographs based on averaging many identical particles.

61 k-filament cross-sectional areas in electron micrographs by 44%.

62 Absorption spectra of different parts of a micrograph can readily be compiled using white-light ill

63 Scanning electron micrographs confirm high imprint fidelity and precision

64 Electron micrographs confirmed the lack of intact presynaptic ter

65 Both amperometry and electron micrograph data were analyzed by statistical and machine

66 evident from pin-holes and eroded surface in micrographs, decreased % crystallinity and FTIR peaks.

67 In electron micrographs, degenerating granule neurons displayed a un

68 uclei in the cyst, and transmission electron micrographs demonstrate fusion between cyst nuclei.

69 case, freeze-fracture transmission electron micrographs demonstrate that at least some of the soluti

70 Electron micrographs demonstrated C3 molecules on the cell wall b

71 Examination of numerous electron micrographs demonstrated that enveloped virions were hou

72 Immunofluorescent confocal micrographs demonstrated the enveloping membranous struc

73 Here we present scanning helium micrographs demonstrating image contrast arising from a

74 SEM micrographs depicted smoother surface for gelatin-MMT an

75 out even quite large components in electron micrographs, despite nominally high resolution.

76 IR and X-ray absorption spectra and electron micrographs determine the structures and locations of th

77 from disc membrane regions on such electron micrographs displayed a diffuse ring at approximately 4.

78 at gastric glands were dilated, and electron micrographs displayed a distinct and striking absence of

79 ns regarding the originality of the electron micrographs displayed in Fig. 1.

80 EM micrographs displayed packets of cellular material conta

81 ree-dimensional reconstruction from electron micrographs due to the fact that projections of these fi

82 Electron micrograph (EM) images of these mutants showed assembled

83 ages from negative-stain electron microscopy micrographs (EM), a 3D density map from single-particle

84 ngle-particle recognition from noisy cryo-EM micrographs, enabling automated particle picking, select

85 ution derived from a tilt series of electron micrographs established the solvent content of the 3D cr

86 Electron micrographs first confirmed that the eukaryotic genome i

87 The electron scanning micrograph for the composite film was homogeneous, witho

88 n Mollicutes has been inferred from electron micrographs for over 50 years without conclusive data to

89 The 130 high resolution electron micrographs from aging rhesus monkey (Macaca mulatta), p

90 Electron micrographs from diabetic eNOS KO mice revealed an injur

91 Transmission electron micrographs from humans and mice treated with imatinib s

92 Electron micrographs from previous studies show these plaques to

93 Electron micrographs from the 1960s revealed the presence of an S

94 e study, we analyze cross-sectional electron micrographs from the fornix of young and old rhesus monk

95 orrelated with organelles imaged in electron micrographs from the same sections.

96 quisition of high-resolution serial electron micrographs from which neuronal arbors can be reconstruc

97 Atomic force microscopy micrographs further support the model of ganglioside-ind

98 , and single-particle processing of electron micrographs gives size estimates of 70-90 kDa.

99 ae and mitochondria (first noted in electron micrographs >50 yr ago) and caveolae-mitochondria intera

100 Transmission electron microscope micrographs have confirmed the presence of wormlike fibr

101 roteins or cellular compartments in electron micrographs, however, remains challenging because of dif

102 from the thin section transmission electron micrograph image (2D) or the "seed and growth" model ima

103 rt a 3D single-particle analysis of electron micrograph images of negatively stained myosin filaments

104 rmity was quantified using scanning electron micrographs in cesa9 epidermal cells.

105 tomated particle extraction from raw cryo-EM micrographs in the absence of a template.

106 Electron micrographs indicate that chlamydiae possess needle fila

107 Hydrodynamic data and electron micrographs indicate that the active state is extended,

108 Image reconstruction from electron micrographs indicates that a symmetric oligomer is prese

109 chloride channel transporters plus electron micrographs indicating enlarged vacuoles suggested vacuo

110 In electron micrographs, individual CAR-deficient cardiomyocytes wit

111 nal methods, we incorporated serial electron micrographs into a three-dimensional reconstruction of t

112 oublecortin domain observed in cryo-electron micrographs is the C-terminal domain rather than the N-t

113 ructions shown in many transmission electron micrographs led to a discussion about the mode of phloem

114 ts striated, periodic appearance in electron micrographs led to the idea that transverse filaments wi

115 Statistical analysis of confocal micrographs obtained from the flow cell biofilms reveale

116 The area of the micrograph occupied by each type was estimated with a po

117 umber initially decreased (relative area per micrograph of 64+/-10% at baseline vs. 39+/-13% at 8 h f

118 1947, Sulzberger and colleagues published a micrograph of a blocked acrosyringium in a patient with

119 hest resolution (11-13 nm) x-ray diffraction micrograph of biological specimens, and a demonstration

120 nce intensity, emulsifying properties, light micrograph of emulsions and in vitro antioxidant activit

121 The field-emission scanning electron micrograph of the surface indicates nanostructured lamel

122 applied correspondence analysis to electron micrographs of 2-D rafts of F-actin cross-linked with al

123 nt enabled serial reconstruction of electron micrographs of a flat, punctate zone, identified during

124 Electron micrographs of a JCSC1435 mutant with a deleted cap regi

125 Interestingly, transmission electron micrographs of abscission zone regions from wild-type an

126 We show that electron micrographs of acrosomal bundles in water are similar to

127 Electron micrographs of aldehyde-fixed control PNJs, in which TBs

128 Electron micrographs of atrial myocytes show peripheral SR cister

129 Scanning electron microscopy micrographs of biofilms exposed to taurocholate revealed

130 Using BRIM, micrographs of biomarkers whose expression correlates wi

131 breast cancer aggressiveness are divided by micrographs of biomarkers whose expression negatively co

132 ars ago by analysis of transmission electron micrographs of bone marrow.

133 The RNP polymer, viewed in electron micrographs of both virus RNP and RNP reconstituted from

134 have aberrant particle morphology; electron micrographs of cells expressing some of these mutants ar

135 rrelative thin-section transmission electron micrographs of cells fixed one second after irradiation

136 Immunofluorescent micrographs of cells treated with cpt-cAMP showed a sign

137 quantitative image analysis of fluorescence micrographs of cells undergoing apoptosis verifies that

138 Atomic-force micrographs of CH3-Ge(111) surfaces indicated that the s

139 Electron micrographs of CIP4-null megakaryocytes showed an altere

140 d generate a vascular area mask (VAM) in H&E micrographs of clear cell renal cell carcinoma (ccRCC) c

141 Micrographs of cultured cells exposed to the nanoparticl

142 In addition, electron micrographs of Drosophila and other flies (e.g. the hous

143 Immuno-electron micrographs of embryos expressing sAnxV::GFP or sGFP::La

144 Electron micrographs of fibroblasts at 3 or 5 days postinfection

145 as from single-molecule imaging and electron micrographs of fixed cells, and provides the mathematica

146 traightforward strategy to calibrate digital micrographs of fluorescent surfaces such as planar cellu

147 ture are produced which are seen in electron micrographs of freeze-fracture replicas with periodiciti

148 nuclear pore, as observed in early electron micrographs of giant Balbiani ring mRNPs.

149 Transmission electron micrographs of GS52 silenced root nodules showed that ea

150 Electron micrographs of hearts from TPC1/2 double knockout mice s

151 The confocal laser scanning micrographs of HeLa cells confirmed the cell permeabilit

152 Micrographs of historical interest are presented that ar

153 l polymer electrolyte membrane from electron micrographs of individual acidic clusters.

154 Electron micrographs of infected cells revealed a large number of

155 Electron micrographs of insect mouthparts indicate that the prism

156 Micrographs of kernel showed pigments concentrated in pe

157 Furthermore, scanning electron micrographs of mitochondria from LKT-treated BL-3 cells

158 Electron micrographs of myosin-18A motor domain-decorated F-actin

159 it corresponds to the hinge seen in electron micrographs of NCAM.

160 The Raman data are supported by electron micrographs of negatively stained specimens of phage fd,

161 Electron micrographs of pancreas depicted macrophages in close co

162 d/pore diffusion mechanism based on confocal micrographs of percolating pores in the polymer, not pre

163 In electron micrographs of permeabilized hippocampal synapses stimul

164 From direct measurements on light micrographs of polytene chromosomes, we then deduce the

165 Flytrap contains two principle data types: micrographs of protein localization and a cellular compo

166 Cryo-electron micrographs of purified Syn5 virions revealed that the c

167 , ZO-1, and Cx43 were analyzed from confocal micrographs of rat fat-pad ECs after 5 h of shear stress

168 3-A crystal structure of RVFV N and electron micrographs of ribonucleoprotein (RNP) reveal an encapsi

169 reported distribution obtained from electron micrographs of RNA polymerase molecules along rrn operon

170 Here we report that electron micrographs of rsh mutant cells lacking RSH extensin cor

171 erminals and their bipolar cells in electron micrographs of serial sections from macaque foveal retin

172 to estimate numbers of synapses in electron micrographs of serial sections processed for postembeddi

173 indles by using reconstruction from electron micrographs of serially sectioned meiotic cells.

174 on of biological molecules from the electron micrographs of single particles.

175 ructures of variable size from cryo-electron micrographs of single particles.

176 ions imaged by light microscopy, or electron micrographs of single ultrathin sections imaged by trans

177 Electron micrographs of SOD2-deficient reticulocytes reveal strik

178 larger serum pores were observed in confocal micrographs of soymilk added with ODPEPS.

179 Electron micrographs of spinal cords immunostained with an anti-G

180 pheroidal fluorescent shell image to optical micrographs of spores incorporating fluorescent fusion p

181 imulations are consistent with cryo-electron micrographs of T7 phage DNA.

182 A series of micrographs of the cells inside of the tubing indicates

183 Electron micrographs of the DeltaalgL mutant showed that alginate

184 Light micrographs of the dorsal root entry zone show the perip

185 Electron micrographs of the F. tularensis LVS Delta ripA mutant d

186 again at Larry's paper, I found the electron micrographs of the kDNA networks to be rather beautiful.

187 Electron micrographs of the mutant revealed larger cells with div

188 llectively, our NMR spectra and the electron micrographs of the purified ECM inspire us to consider t

189 Electron micrographs of the purified inflammasome provide unprece

190 yx depth (0.078 +/- 0.016 mum) from electron micrographs of the same portion of the same vessel.

191 ed from this growth model, polarized optical micrographs of the self-assembled fibrillar networks (SA

192 nsions to 23 A resolution from cryo-electron micrographs of the singly bound complex, PA200 has an as

193 Electron micrographs of the variant operon suggest that the 23S r

194 Image reconstructions of cryoelectron micrographs of three ACA-D viruses that each contain a s

195 Cryo-electron micrographs of tilted Afp specimens (up to 60 degrees) w

196 In this study, we used electron micrographs of tissues prepared using perfusion fixation

197 Electron micrographs of toxin-induced cells showed no obvious mem

198 Higher quality micrographs of untilted specimens were processed to prod

199 NM IIA and NM IIB typically seen in confocal micrographs of well-polarized cells is reflected in the

200 density distribution of A-bands in electron micrographs of well-preserved specimens.

201 However, electron micrographs of WPBs at the Golgi apparatus show that the

202 epository of biological images, housing 1500 micrographs of yeast cells carrying stained proteins.

203 Electron micrographs of ZapA-bundled FtsZ filaments showed the mo

204 Electron micrographs offer clear evidence of pores created on cel

205 peptides formed fibrils visible in electron micrographs or needle-like microcrystals showing a cross

206 tations to terrace heights from atomic force micrographs proves that the end chains are interdigitate

207 tailed schematic drawings and representative micrographs provide examples of how best to identify hum

208 The CLSM micrographs provided evidence of the substantial disinte

209 Micrographs provided images of the changing morphology o

210 lates with aggressiveness to create computed micrographs reflecting aggressiveness.

211 ree filaments seen in lamellipodial electron micrographs, requiring approximately 12 generations of s

212 Negative-stain electron micrographs reveal that filaments are apolar and made of

213 In addition, electron micrographs reveal the formation of tubular myelin struc

214 and E-cadherin, was increased, and electron micrographs revealed an apico-basal diffusion of AJs.

215 Proximate analysis and light micrographs revealed higher migration of red rice protei

216 Electron micrographs revealed large spaces between axons and 32%

217 Electron micrographs revealed lipid and mitochondrial abnormaliti

218 sputtering deposition and scanning electron micrographs revealed nano-clusters of metal catalyst in

219 Scanning electron micrographs revealed presence of dents and fusion of ric

220 Electron micrographs revealed stratified constructs with multiple

221 Electron micrographs revealed that both water-deprived and NaCl-t

222 Electron micrographs revealed that D. mccartyi were abundant with

223 Scanning electron micrographs revealed that hair bundles exposed to fragme

224 Furthermore, scanning electron micrographs revealed that KasA depletion resulted in the

225 Light micrographs revealed that NaCl roughened the surface of

226 Scanning electron micrographs revealed that the sonicated protein isolates

227 Electron micrographs revealed that vesicular pools were not reduc

228 Electron micrographs revealed the cytoplasmic accumulation of lip

229 ult male, reconstructed from serial electron micrograph sections.

230 cluded are high-resolution scanning electron micrograph (SEM) images of the surface structures, along

231 dpoles (EC(50) = 16 microM) and fluorescence micrographs show 1-AMA localized to brain and olfactory

232 Individual micrographs show clear ultrastructure that allowed direc

233 Electron micrographs show direct contact between endothelial cell

234 Electron micrographs show mitochondria with swollen matrices that

235 Electron micrographs show morphological features indicating a pro

236 Cryo-TEM micrographs show that SWNTs stabilized using p-PNCPA tra

237 ee-dimensional reconstructions from electron micrographs show that this peptide binds to the RAD-51 N

238 Time-lapse AFM micrographs show this change in height in real time.

239 Scanning electron micrograph showed well-shaped and smooth spherical morph

240 SPEF micrographs showed a decrease in cellular area followed

241 Scanning electron micrographs showed a protective shield of CP around the

242 Electron micrographs showed a stepwise entry and fusion of vacuol

243 Additionally, immunoelectron micrographs showed A9 in tubules containing protein disu

244 Electron micrographs showed collapsed capillaries, extensive foot

245 rved in SDS-PAGE while transmission electron micrographs showed complete dispersion of aggregates and

246 ster loaded saponin micelles (LMS), cryo-TEM micrographs showed depending on the composition of the m

247 Micrographs showed different mechanisms of actuation of

248 Scanning electron micrographs showed H. pylori arranged in a matrix on the

249 Electron micrographs showed human fetal muscle myofibrils elongat

250 Electron micrographs showed human fetal muscle sarcomeres are not

251 Scanning electron micrographs showed marked improvement in regular three-d

252 Optical micrographs showed that lime disrupted the integrity of

253 The cryo-SEM and CLSM micrographs showed that minimum porosity was observed at

254 Thin-section electron micrographs showed that mutant cells did not fully separ

255 Electron micrographs showed that nebulin associates with elongate

256 Anterior view micrographs showed that posterior zonular fibers origina

257 rthermore, serial reconstruction of electron micrographs showed that postsynaptic cisterns of BKalpha

258 Electron micrographs showed that the alternative conformations fo

259 Electron micrographs showed that these side polar filaments are v

260 e construct, whereas quick-freeze, deep-etch micrographs showed the details of the matrix interaction

261 Observations are supported by micrographs showing coherent networks with reduced size

262 ting a steady SPR signal decrease, with SPEF micrographs showing extensive collapse of cell actin str

263 ophages in this process is supported only by micrographs showing their association with apoptotic-app

264 ve zone structure, as visualized by electron micrographs, suggesting that their contribution to activ

265 Micrographs taken during the first 4 days during healing

266 collagen fibers and their appearance in the micrographs taken with the atomic force microscope.

267 Transmission electron micrographs (TEM) of infected cells treated with endocyt

268 Transmission electron micrographs (TEMs) were analyzed to determine fibril pos

269 Fluorescence micrographs, TGA, DSC and FTIR spectra suggested the hyp

270 era, they assembled a stunning collection of micrographs that illustrated how L. monocytogenes enters

271 of approximately 10 nm were also observed in micrographs that were attributed to alpha-lac/CMD-b-PEG

272 In electron micrographs the M/T to granule cell synapse appeared to

273 In electron micrographs, the AC is a highly vacuolated part of the c

274 In light micrographs, the density of TM radial collagen fibers wa

275 number of mitochondrial profiles in electron micrographs, the levels of selected energy metabolites a

276 tion; from the model of producing only a few micrographs, through the current state where many images

277 Particle extraction from experimental micrographs thus can be laborious and presents a major p

278 by taking a series of transmission electron micrographs tilted at different angles in vitreous ice:

279 whose size distribution is shown by electron micrographs to be skewed.

280 ensional reconstruction from serial electron micrographs to investigate two structural changes that c

281 of the Z-band in transverse-section electron micrographs typically resembles a small-square lattice o

282 rientations determined from particles on one micrograph using the map, the agreement (average phase r

283 easuring their length, diameter, and area on micrographs using imaging software.

284 Together with electron micrographs, visual inspection, and contact angle measur

285 on the appearance of nerve fibers in corneal micrographs was explored.

286 From analysis of scanning electron micrographs, we find that median microvillar length and

287 partial reconstructions from serial electron micrographs, we quantify synaptic circuits for two other

288 By reconstruction from serial electron micrographs, we show that L- and M-cone pedicles in maca

289 Two-dimensional micrographs were collated into a three-dimensional array

290 Additional cross-section micrographs were collected at 10- or 20-microm intervals

291 m to overcome many of these problems.Digital micrographs were obtained from cone photoreceptor mosaic

292 ve samples, light, and transmission electron micrographs were used to evaluate optic atrophy postmort

293 The article uses several electron micrographs which have been used in other publications a

294 le to obtain phase-contrast and fluorescence micrographs with more than 18,000 single cells per image

295 eld multi-pass polarization and transmission micrographs with variance reductions of 4.4+/-0.8 dB (11

296 ation of the IM (up to 19 layers in electron micrographs) without significant effects on plant growth

297 Scanning electron micrographs, x-ray diffraction spectra, x-ray photoelect

298 red by (29)Si-MAS NMR, transmission electron micrographs, X-ray diffraction, and adsorption isotherms

299 this molecular assembly in negative-stained micrographs yielded a three-dimensional asymmetric recon

300 averaging of small subsets of digitized TEM micrographs yields an averaged projection image that is