ライフサイエンスコーパス: electron micrograph

1 les the characteristic footprint seen in the electron micrograph.

2 a new dataset of 16227 scanning transmission electron micrographs.

3 ensional reconstructions from serial-section electron micrographs.

4 r the nanoscopic localization of proteins in electron micrographs.

5 nd a presynaptic dense projection protein in electron micrographs.

6 at previously estimated from the analysis of electron micrographs.

7 th basal dendrites reconstructed from serial electron micrographs.

8 oncentric rings when reconstructed from cryo-electron micrographs.

9 s, confirming findings that we obtained from electron micrographs.

10 os, and exhibited thicker fibers in scanning electron micrographs.

11 al repair was observed in nemaline muscle in electron micrographs.

12 explanation for the small ECS visualized in electron micrographs.

13 crystalline aggregates of protein and DNA in electron micrographs.

14 periodically arranged troponin complexes in electron micrographs.

15 rk-staining outer spore coat in thin-section electron micrographs.

16 apsids from cryo-negative stain transmission electron micrographs.

17 eurotransmitter release as well as examining electron micrographs.

18 uick assessment, sorting and hole masking of electron micrographs.

19 to be identical to the wild-type virions in electron micrographs.

20 , thereby facilitating interpretation of the electron micrographs.

21 it bridges that are visible in reconstructed electron micrographs.

22 e-dimensional (3D) image reconstruction from electron micrographs.

23 ls constructed from stereo pairs of scanning electron micrographs.

24 he whole myosin-I tail in reconstructions of electron micrographs.

25 and performed unbiased disector counts from electron micrographs.

26 500 individual particles extracted from cryo-electron micrographs.

27 tructures that could be seen in thin-section electron micrographs.

28 le cell layer were reconstructed from serial electron micrographs.

29 coarse subunit mapping onto 2-D images from electron micrographs.

30 e folds independently of their appearance in electron micrographs.

31 n osmiophilic precipitate that is visible in electron micrographs.

32 racterization of the leaves and to light and electron micrographs.

33 e particles with low detergent background in electron micrographs.

34 ic cells and reconstructed in 3D from serial electron micrographs.

35 ermined by single-particle reconstruction of electron micrographs a low-resolution, 3D structure of S

36 Correlation of immunofluorescent and electron micrographs allowed high resolution imaging of

37 On electron micrographs an average filament length of appro

38 Electron micrographs and biochemical data with a PFKL/PF

39 smooth muscle cells (SMCs) were observed in electron micrographs and by confocal microscopy.

40 We demonstrate by cryo electron micrographs and elongated tracer particles imag

41 Electron micrographs and immunofluorescence staining of

42 ascent flagellar filaments became visible in electron micrographs and over 40% of the cells exhibited

43 Electron micrographs and quantitative measurements show

44 9 mature seeds supported results of scanning electron micrographs and quantitatively showed depletion

45 microscopy, x-ray diffraction, simulation of electron micrographs, and molecular model building was u

46 r VGlut1-positive puncta, larger profiles in electron micrographs, and more release sites per profile

47 properties of a dimer, appears as a dimer in electron micrographs, and moves processively on actin fi

48 However, conventional electron micrographs are simply two-dimensional projecti

49 t molecules and PD dimensions (measured from electron micrographs) are both used as methods to predic

50 Helical 3D reconstruction from electron micrographs at 20 A resolution provides a struc

51 As observed in cryo-electron micrographs, AVP-p treatment causes morphologic

52 ructural analysis by image reconstruction of electron micrographs based on averaging many identical p

53 uced thick-filament cross-sectional areas in electron micrographs by 44%.

54 Scanning electron micrographs confirm high imprint fidelity and p

55 Electron micrographs confirmed the lack of intact presyn

56 Both amperometry and electron micrograph data were analyzed by statistical an

57 Using an electron micrograph dataset for an entire Drosophila mel

58 In electron micrographs, degenerating granule neurons displ

59 between nuclei in the cyst, and transmission electron micrographs demonstrate fusion between cyst nuc

60 he latter case, freeze-fracture transmission electron micrographs demonstrate that at least some of t

61 Electron micrographs demonstrated C3 molecules on the ce

62 Examination of numerous electron micrographs demonstrated that enveloped virions

63 Quantitative analysis of the electron micrographs demonstrated that the starch conten

64 t to pick out even quite large components in electron micrographs, despite nominally high resolution.

65 IR and X-ray absorption spectra and electron micrographs determine the structures and locati

66 alculated from disc membrane regions on such electron micrographs displayed a diffuse ring at approxi

67 icated that gastric glands were dilated, and electron micrographs displayed a distinct and striking a

68 nt concerns regarding the originality of the electron micrographs displayed in Fig. 1.

69 ve for three-dimensional reconstruction from electron micrographs due to the fact that projections of

70 Electron micrograph (EM) images of these mutants showed

71 Using serial electron micrograph (EM) reconstruction, we re-evaluate

72 ane resolution derived from a tilt series of electron micrographs established the solvent content of

73 Electron micrographs extended these findings and reveale

74 Electron micrographs first confirmed that the eukaryotic

75 e (EPS) in Mollicutes has been inferred from electron micrographs for over 50 years without conclusiv

76 The 130 high resolution electron micrographs from aging rhesus monkey (Macaca mu

77 Electron micrographs from diabetic eNOS KO mice revealed

78 Transmission electron micrographs from humans and mice treated with i

79 Electron micrographs from previous studies show these pl

80 te realistic 512 x 512 scanning transmission electron micrographs from spiral, jittered gridlike, and

81 Electron micrographs from the 1960s revealed the presenc

82 As a case study, we analyze cross-sectional electron micrographs from the fornix of young and old rh

83 escence correlated with organelles imaged in electron micrographs from the same sections.

84 -scale acquisition of high-resolution serial electron micrographs from which neuronal arbors can be r

85 nal processes and synaptic connections using electron micrographs generated in a previous study of th

86 d 110 kDa, and single-particle processing of electron micrographs gives size estimates of 70-90 kDa.

87 nanometer scale crystallographic defects in electron micrographs governed by complex contrast mechan

88 ne caveolae and mitochondria (first noted in electron micrographs >50 yr ago) and caveolae-mitochondr

89 pecific proteins or cellular compartments in electron micrographs, however, remains challenging becau

90 "learns" from the thin section transmission electron micrograph image (2D) or the "seed and growth"

91 In one study, electron micrograph image averages of the headpiece of i

92 h simulations requires watertight meshing of electron micrograph images into 3D volume meshes, which

93 Past attempts to detect tropomyosin in electron micrograph images of frozen-hydrated troponin-r

94 e we report a 3D single-particle analysis of electron micrograph images of negatively stained myosin

95 Single particle analysis of the resulting electron micrograph images, to which no symmetry was app

96 With three-dimensional reconstruction of electron micrograph images, we show that Hib pili compri

97 gle uniformity was quantified using scanning electron micrographs in cesa9 epidermal cells.

98 Electron micrographs indicate that chlamydiae possess ne

99 Hydrodynamic data and electron micrographs indicate that the active state is e

100 s, as well as images from negatively stained electron micrographs, indicate that pore formation is as

101 atment reversibly inhibited vesicle cycling; electron micrographs indicated a dramatic reduction in t

102 Electron micrographs indicated that modified epithelial

103 Image reconstruction from electron micrographs indicates that a symmetric oligomer

104 ar NO3(-) chloride channel transporters plus electron micrographs indicating enlarged vacuoles sugges

105 In electron micrographs, individual CAR-deficient cardiomyo

106 omputational methods, we incorporated serial electron micrographs into a three-dimensional reconstruc

107 tion achieved in the image processing of the electron micrographs is on the order of 9 A in the merid

108 anisms in stained smears and in transmission electron micrographs is that of P. carinii, and P. carin

109 racting doublecortin domain observed in cryo-electron micrographs is the C-terminal domain rather tha

110 tein obstructions shown in many transmission electron micrographs led to a discussion about the mode

111 Its striated, periodic appearance in electron micrographs led to the idea that transverse fil

112 n than electrons per atom contributing to an electron micrograph may enable diffraction measurements

113 The field-emission scanning electron micrograph of the surface indicates nanostructu

114 We have applied correspondence analysis to electron micrographs of 2-D rafts of F-actin cross-linke

115 arrangement enabled serial reconstruction of electron micrographs of a flat, punctate zone, identifie

116 Electron micrographs of a JCSC1435 mutant with a deleted

117 Interestingly, transmission electron micrographs of abscission zone regions from wil

118 We show that electron micrographs of acrosomal bundles in water are s

119 An analysis of electron micrographs of Al5Mn quasicrystals obtained by

120 Electron micrographs of aldehyde-fixed control PNJs, in

121 Electron micrographs of at least 15 keratocytes each fro

122 Electron micrographs of atrial myocytes show peripheral

123 ry of cytochrome oxidase, and morphometry of electron micrographs of biopsy specimens to determine wh

124 bed 50 years ago by analysis of transmission electron micrographs of bone marrow.

125 The RNP polymer, viewed in electron micrographs of both virus RNP and RNP reconstit

126 In addition, electron micrographs of Cav-1-deficient lung capillaries

127 brane and have aberrant particle morphology; electron micrographs of cells expressing some of these m

128 Correlative thin-section transmission electron micrographs of cells fixed one second after irr

129 Electron micrographs of cells infected with the delta vp

130 Electron micrographs of CIP4-null megakaryocytes showed

131 Electron micrographs of crosslinked, rotary shadowed spe

132 On the basis of our kinetic results and electron micrographs of depolymerizing fibers, we propos

133 ch calculations that image reconstruction of electron micrographs of disulfide cross-linked C41-C374

134 In addition, electron micrographs of Drosophila and other flies (e.g.

135 Immuno-electron micrographs of embryos expressing sAnxV::GFP or

136 Electron micrographs of fibroblasts at 3 or 5 days posti

137 as well as from single-molecule imaging and electron micrographs of fixed cells, and provides the ma

138 ple structure are produced which are seen in electron micrographs of freeze-fracture replicas with pe

139 rough the nuclear pore, as observed in early electron micrographs of giant Balbiani ring mRNPs.

140 s in the junctional structure discernible in electron micrographs of glutaraldehyde-fixed cell materi

141 Transmission electron micrographs of GS52 silenced root nodules showe

142 Electron micrographs of hearts from TPC1/2 double knocko

143 Electron micrographs of HRP-containing axons as well as

144 in a model polymer electrolyte membrane from electron micrographs of individual acidic clusters.

145 Electron micrographs of infected cells revealed a large

146 Electron micrographs of infectious virions depict partic

147 Electron micrographs of insect mouthparts indicate that

148 y, using three-dimensional reconstruction of electron micrographs of interacting filaments, we have b

149 Electron micrographs of livers from TgBP-1a mice showed

150 In electron micrographs of longitudinal sections of fast fi

151 Scanning electron micrographs of lung tissue, focusing on the int

152 Furthermore, scanning electron micrographs of mitochondria from LKT-treated BL

153 o-stained histological sections and scanning electron micrographs of multiple stages of salivary glan

154 Electron micrographs of myosin-18A motor domain-decorate

155 ing that it corresponds to the hinge seen in electron micrographs of NCAM.

156 Electron micrographs of negatively stained E. faecalis c

157 Electron micrographs of negatively stained intact flagel

158 aments to c. 26 A resolution determined from electron micrographs of negatively stained preparations

159 The Raman data are supported by electron micrographs of negatively stained specimens of

160 ipt cleavage factor GreB was determined from electron micrographs of negatively stained, flattened he

161 n of a workflow using GAMer 2 to a series of electron micrographs of neuronal dendrite morphology exp

162 Scanning electron micrographs of neutrophils rolling on P-selecti

163 Electron micrographs of osmotically shocked cells showed

164 Electron micrographs of pancreas depicted macrophages in

165 In electron micrographs of permeabilized hippocampal synaps

166 Cryo-electron micrographs of purified Syn5 virions revealed t

167 In electron micrographs of quick-frozen, deep-etched sample

168 The 1.93-A crystal structure of RVFV N and electron micrographs of ribonucleoprotein (RNP) reveal a

169 alyzed a reported distribution obtained from electron micrographs of RNA polymerase molecules along r

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

171 us cone terminals and their bipolar cells in electron micrographs of serial sections from macaque fov

172 were used to estimate numbers of synapses in electron micrographs of serial sections processed for po

173 Using three-dimensional reconstructions from electron micrographs of serial transverse sections, amph

174 15 MII spindles by using reconstruction from electron micrographs of serially sectioned meiotic cells

175 region T(iii) observed in computer-processed electron micrographs of sigma1 protein purified from vir

176 onstruction of biological molecules from the electron micrographs of single particles.

177 rating structures of variable size from cryo-electron micrographs of single particles.

178 ned by three-dimensional reconstruction from electron micrographs of single particles.

179 ical sections imaged by light microscopy, or electron micrographs of single ultrathin sections imaged

180 Electron micrographs of SOD2-deficient reticulocytes rev

181 Electron micrographs of spike protein suggests that hepa

182 Electron micrographs of spinal cords immunostained with

183 from T7 simulations are consistent with cryo-electron micrographs of T7 phage DNA.

184 Electron micrographs of the arrays are suitable for heli

185 immunostaining of fimbrial preparations and electron micrographs of the bacteria, revealed that surf

186 Diffraction from electron micrographs of the crystals in negative stain e

187 Electron micrographs of the DeltaalgL mutant showed that

188 article reconstruction from negative-stained electron micrographs of the ectodomain and multidomain c

189 Electron micrographs of the F. tularensis LVS Delta ripA

190 This model is consistent with the electron micrographs of the fibre and it was supported b

191 labelled His tag by statistical analysis of electron micrographs of the gold-labelled photosystem II

192 Looking again at Larry's paper, I found the electron micrographs of the kDNA networks to be rather b

193 Electron micrographs of the mutant revealed larger cells

194 Collectively, our NMR spectra and the electron micrographs of the purified ECM inspire us to c

195 Electron micrographs of the purified inflammasome provid

196 glycocalyx depth (0.078 +/- 0.016 mum) from electron micrographs of the same portion of the same ves

197 hree dimensions to 23 A resolution from cryo-electron micrographs of the singly bound complex, PA200

198 of mitochondrial membrane integrity seen in electron micrographs of the transplanted 48-hr group.

199 Electron micrographs of the variant operon suggest that

200 Immuno-electron micrographs of thin sections of rat atrial myoc

201 Electron micrographs of this complex are presented, and

202 Cryo-electron micrographs of tilted Afp specimens (up to 60 d

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

204 Electron micrographs of toxin-induced cells showed no ob

205 Transmission electron micrographs of type I collagen fibrils in a pro

206 structure of the heterodimer determined from electron micrographs of unstained frozen-hydrated tubula

207 Image reconstructions of electron micrographs of virus particles containing wild-

208 the axial density distribution of A-bands in electron micrographs of well-preserved specimens.

209 However, electron micrographs of WPBs at the Golgi apparatus show

210 Electron micrographs of ZapA-bundled FtsZ filaments show

211 Electron micrographs offer clear evidence of pores creat

212 Transmission electron micrographs on thin films of these composites s

213 loid-like peptides formed fibrils visible in electron micrographs or needle-like microcrystals showin

214 Based on electron micrographs, PAN and PAN(Delta1-73) apparently

215 +/-35 degree filaments seen in lamellipodial electron micrographs, requiring approximately 12 generat

216 Three-dimensional reconstructions of electron micrographs reveal a conformational difference

217 Negative-stain electron micrographs reveal that filaments are apolar an

218 Cryo-electron micrographs reveal that the V18S substitution c

219 In addition, electron micrographs reveal the formation of tubular mye

220 a-catenin and E-cadherin, was increased, and electron micrographs revealed an apico-basal diffusion o

221 Electron micrographs revealed erythrostasis in tumor mic

222 In this study, electron micrographs revealed fusion of differentiated m

223 Electron micrographs revealed large spaces between axons

224 Electron micrographs revealed lipid and mitochondrial ab

225 by plasma sputtering deposition and scanning electron micrographs revealed nano-clusters of metal cat

226 Scanning electron micrographs revealed presence of dents and fusi

227 Electron micrographs revealed stratified constructs with

228 Electron micrographs revealed that both water-deprived a

229 Electron micrographs revealed that D. mccartyi were abun

230 Scanning electron micrographs revealed that hair bundles exposed

231 Furthermore, scanning electron micrographs revealed that KasA depletion result

232 Scanning electron micrographs revealed that modified okara partic

233 Scanning electron micrographs revealed that the sonicated protein

234 Electron micrographs revealed that vesicular pools were

235 Immunogold labelling in electron micrographs revealed that YSD1_22 forms the mai

236 Electron micrographs revealed the cytoplasmic accumulati

237 citatory synapses, reconstructed from serial electron micrograph sections of mouse brain, and have co

238 legans adult male, reconstructed from serial electron micrograph sections.

239 Included are high-resolution scanning electron micrograph (SEM) images of the surface structur

240 3D reconstruction from electron micrographs show a two-layer "simple" Z-band in

241 Electron micrographs show direct contact between endothe

242 Electron micrographs show mitochondria with swollen matr

243 Electron micrographs show morphological features indicat

244 ation of DNA-containing nuclear capsids, but electron micrographs show no enveloped virus particles i

245 Published x-ray diagrams and electron micrographs show that fibers of synuclein, the

246 Electron micrographs show that the 100-A-thick fibers of

247 Electron micrographs show that the virion consists of a

248 Three-dimensional reconstructions from electron micrographs show that this peptide binds to the

249 Scanning electron micrograph showed well-shaped and smooth spheri

250 Scanning electron micrographs showed a protective shield of CP ar

251 Electron micrographs showed a stepwise entry and fusion

252 Electron micrographs showed collapsed capillaries, exten

253 was observed in SDS-PAGE while transmission electron micrographs showed complete dispersion of aggre

254 tion isotherms, polarized light and scanning electron micrographs showed crystallized lactose in low

255 Electron micrographs showed gross abnormalities in the c

256 Scanning electron micrographs showed H. pylori arranged in a matr

257 Electron micrographs showed human fetal muscle myofibril

258 Electron micrographs showed human fetal muscle sarcomere

259 Scanning electron micrographs showed marked improvement in regula

260 Electron micrographs showed no significant difference in

261 Three-dimensional maps computed from electron micrographs showed that all three viruses have

262 Electron micrographs showed that at physiological molar

263 Electron micrographs showed that in spoIIB mutant sporan

264 Thin-section electron micrographs showed that mutant cells did not fu

265 Electron micrographs showed that nebulin associates with

266 Furthermore, serial reconstruction of electron micrographs showed that postsynaptic cisterns o

267 Electron micrographs showed that the alternative conform

268 Electron micrographs showed that the bottom and top meta

269 Electron micrographs showed that these side polar filame

270 Electron micrographs showed the presence of the insectic

271 t on active zone structure, as visualized by electron micrographs, suggesting that their contribution

272 e, the presence of intact axonal profiles in electron micrographs taken at the lesion site, and/or th

273 Transmission electron micrographs (TEM) of infected cells treated wit

274 Transmission electron micrographs (TEMs) were analyzed to determine f

275 In electron micrographs the M/T to granule cell synapse app

276 In electron micrographs, the AC is a highly vacuolated part

277 In negatively stained electron micrographs, the isolated needles were 60-80 nm

278 for the number of mitochondrial profiles in electron micrographs, the levels of selected energy meta

279 regular patterns seen in transverse section electron micrographs; the so-called small-square and bas

280 In electron micrographs these filaments appeared sometimes

281 nnels are recognizable in negatively stained electron micrographs, these lattices are disordered and

282 To aid interpretation of electron micrographs, three-dimensional model toroids we

283 achieved by taking a series of transmission electron micrographs tilted at different angles in vitre

284 (BLiPs), whose size distribution is shown by electron micrographs to be skewed.

285 lly, we used serial morphometric analysis of electron micrographs to explore the basis for the progre

286 in the form of rings, which were observed in electron micrographs to have outside and inside diameter

287 three-dimensional reconstruction from serial electron micrographs to investigate two structural chang

288 23)C(6) crystals, measured from transmission electron micrographs, to be from 10 to 30 nm.

289 pearance of the Z-band in transverse-section electron micrographs typically resembles a small-square

290 nalysis of both new and previously published electron micrographs update previous results and include

291 Together with electron micrographs, visual inspection, and contact ang

292 rmine the lattice dimensions and analysis of electron micrographs was used to determine the lattice s

293 From analysis of scanning electron micrographs, we find that median microvillar le

294 based on partial reconstructions from serial electron micrographs, we quantify synaptic circuits for

295 By reconstruction from serial electron micrographs, we show that L- and M-cone pedicle

296 optic nerve samples, light, and transmission electron micrographs were used to evaluate optic atrophy

297 The article uses several electron micrographs which have been used in other publi

298 proliferation of the IM (up to 19 layers in electron micrographs) without significant effects on pla

299 Scanning electron micrographs, x-ray diffraction spectra, x-ray p

300 as monitored by (29)Si-MAS NMR, transmission electron micrographs, X-ray diffraction, and adsorption