ライフサイエンスコーパス: electron microscopy

1 scopy, dynamic light scattering and scanning electron microscopy.

2 n-based diffraction and aberration corrected electron microscopy.

3 l as pyramidal, MN, as confirmed by scanning electron microscopy.

4 ospheric pressure, by using advanced in situ electron microscopy.

5 ution, as determined by single-particle cryo-electron microscopy.

6 ssion of the capsid protein, using cryogenic electron microscopy.

7 y, and high-resolution scanning transmission electron microscopy.

8 )1+delta ]n (TiSe2 )1 heterostructures using electron microscopy.

9 n of biochemical techniques and transmission electron microscopy.

10 surface morphology was evaluated by scanning electron microscopy.

11 visualized using serial block-face scanning electron microscopy.

12 d for paraffin embedding or for transmission electron microscopy.

13 nd examined by fluorescent, brightfield, and electron microscopy.

14 ctroscopy, ESI-MS, TWIM-MS, and transmission electron microscopy.

15 of the treated bacteria revealed by scanning electron microscopy.

16 revisiae Pol II-Rad26 complex solved by cryo-electron microscopy.

17 using low-energy electron and photoemission electron microscopy.

18 led at 673 K for 8-360 hours and analyzed by electron microscopy.

19 ild-type virus as determined by transmission electron microscopy.

20 techniques and high resolution transmission electron microscopy.

21 and contrasted in real time via liquid cell electron microscopy.

22 ose microfibril formation using transmission electron microscopy.

23 confocal, superresolution, and transmission electron microscopy.

24 poorly structured dodecamer as visualized by electron microscopy.

25 was quantitated using confocal and scanning electron microscopy.

26 (PSI) and two PSII monomers as deduced from electron microscopy.

27 and sensory cortices using three-dimensional electron microscopy.

28 llected by focused ion-beam milling scanning electron microscopy.

29 In real time and space, four-dimensional electron microscopy (4D EM) has enabled observation of t

30 lerotic plaques using three-dimensional (3D) electron microscopy, a method never used in this context

31 iens VirB/VirD4 OMCC, solved by transmission electron microscopy, adopts a cage structure similar to

32 ond harmonic generation imaging and scanning electron microscopy, among other vital biological readou

33 Also, mass spectrometry, flow cytometry, and electron microscopy analyses indicated that Cavin-2 is s

34 Electron microscopy analysis of ADHE-enriched stromal fr

35 Correlative light and electron microscopy analysis of infected cells illustrat

36 the entire region combined with quantitative electron microscopy analysis of the full set of mutants

37 Finally, transmission electron microscopy analysis revealed the effect of the

38 Electron microscopy analysis suggested that Pre-F-GCN4t

39 ents, Hall effect measurements, transmission electron microscopy analysis, and first-principles calcu

40 myocytes; a median separation of 20 nm in 2D electron microscopy and 3.3 nm in 3D electron tomography

41 termined to a resolution of 3.1 A using cryo-electron microscopy and 3.8 A by X-ray crystallography.

42 For validation we used mutagenesis, electron microscopy and biochemical assays under non-den

43 e also examined by scanning and transmission electron microscopy and by staining of filamentous actin

44 3+/-4.2mv as characterized with transmission electron microscopy and dynamic light scattering.

45 s were examined by bright-field transmission electron microscopy and electron diffraction.

46 We present chemical (scanning electron microscopy and electron microprobe) and structu

47 Scanning transmission electron microscopy and energy-dispersive X-ray spectros

48 We used transmission electron microscopy and immunohistochemistry to evaluate

49 We employ in-situ transmission electron microscopy and operando X-ray absorption struct

50 over time and samples collected for scanning electron microscopy and RNA sequencing.

51 The transmission electron microscopy and selected-area electron diffracti

52 Immuno-electron microscopy and super-resolution imaging show th

53 rations were characterized with transmission electron microscopy and thioflavin T fluorescence.

54 Using cryo-electron microscopy and time-resolved small-angle X-ray

55 Here, we use serial section electron microscopy and tomography of staged C. elegans

56 sigma(70) determined by single-particle cryo-electron microscopy and validation of the structure usin

57 motif (MBM) assembling around MTs using cryo-electron microscopy and verified it with chemical cross-

58 Transmission electron microscopy and x-ray absorption fine structure

59 d better morphology (confirmed with scanning electron microscopy) and higher in vitro basal insulin r

60 ring, dynamic light scattering, transmission electron microscopy, and a single-crystal X-ray structur

61 lipophilic dye FM1-43 with photoconversion, electron microscopy, and electrophysiology to monitor ev

62 aluminum to copper joints using transmission electron microscopy, and found a 10 nm thick transition

63 ay diffraction, high-resolution transmission electron microscopy, and high-resolution scanning transm

64 tion of approaches (non-invasive imaging, 3D-electron microscopy, and mathematical modelling) to show

65 ods, including atomic force microscopy, cryo-electron microscopy, and neutron scattering, to investig

66 netics, fluorescence microscopy, kymography, electron microscopy, and sensory behavioral assays.

67 mbining live-cell imaging, correlative light electron microscopy, and single-cell analysis, we found

68 ular fiducial marks for single particle cryo-electron microscopy approaches.

69 Using confocal and electron microscopy as well as mathematical analyses, we

70 e we use thioflavin T staining, transmission electron microscopy, as well as ion mobility-mass spectr

71 physical measurements, super-resolution, and electron microscopy, as well as numerical simulations of

72 identical location transmission and scanning electron microscopy, as well as X-ray absorption spectro

73 ing a biofilm device and studied by scanning electron microscopy at 2, 5, and 10 days.

74 t study, bacterial biofilm was visualized by electron microscopy at the surface of AD skin.

75 structural investigations using transmission electron microscopy at various locations to reveal the o

76 At the concentrations used in cryo-electron microscopy, Bim1 causes the compaction of yeast

77 molecules were visualized with transmission electron microscopy, but found to convert readily into c

78 native mass spectrometry and high resolution electron microscopy can define the subunit topology and

79 X-ray crystallography and cryo-transmission electron microscopy can identify metal atoms on protein

80 ron backscatter diffraction and transmission electron microscopy) characterization of the recovered p

81 X-ray diffraction and transmission electron microscopy characterizations indicate that this

82 Here, we used electron microscopy combined with genetic labeling to de

83 graphy, circular dichroism spectroscopy, and electron microscopy; compared the properties of the reco

84 Confocal and scanning electron microscopy confirm removal of biofilm matrix co

85 Electron microscopy confirmed that the surrounding epith

86 In this work, we demonstrate that cryo-electron microscopy (cryo-EM) can be used to image nanos

87 Cryo-electron microscopy (cryo-EM) had played a central role

88 eling of macromolecular structures into cryo-electron microscopy (cryo-EM) maps is a major challenge,

89 Here, we report high resolution cryo electron microscopy (cryo-EM) maps of wild type CPMV con

90 ave obtained high-resolution (3.9-4.2A) cryo-electron microscopy (cryo-EM) reconstructions of MTs sta

91 ough which we present a high-resolution cryo-electron microscopy (cryo-EM) structure of the core tetr

92 Here, we report the cryo-electron microscopy (cryo-EM) structure of the Csy compl

93 one of the largest viruses analyzed by cryo-electron microscopy (cryo-EM) to date.

94 e our protocol for correlated cryo-fLM, cryo-electron microscopy (cryo-EM), and cryo-ET (i.e., cryo-C

95 Combining constraints from ssNMR and cryo-electron microscopy (cryo-EM), we establish an atomic re

96 nly resolved at moderate resolutions by cryo-electron microscopy (cryo-EM).

97 Transmission electron microscopy dark field images confirmed the seco

98 Electron microscopy demonstrated polySia at sites that i

99 Single-particle electron microscopy demonstrated that AKAP79 constrains

100 Immunogold electron microscopy demonstrated that E4 34K is located

101 Transmission electron microscopy demonstrated that sorafenib caused v

102 dynamic light scattering and negative stain electron microscopy demonstrated that zinc ions induce a

103 structure of this complex by negative stain electron microscopy, demonstrating that two copies of Vi

104 rse-grained models are compared with 3D cryo-electron microscopy density maps for these five DNA nano

105 2@PEI MPs) were characterized using scanning electron microscopy, dynamic light scattering, and zeta

106 Using electron microscopy, electrophysiology, and dynamic imag

107 Quantitative electron microscopy (EM) analysis revealed age-dependent

108 zed to decipher neuronal circuits, including electron microscopy (EM) and light microscopy (LM).

109 rth and eye opening, using serial block-face electron microscopy (EM) and RNA sequencing.

110 On virions, electron microscopy (EM) and tomography reveal monomeric

111 Progress in 3D electron microscopy (EM) imaging has greatly facilitated

112 During the last decade, high resolution electron microscopy (EM) of serial sections has become t

113 Fluorescence microscopy (FM) and electron microscopy (EM) offer complementary advantages

114 copic scale, pathology traditionally employs electron microscopy (EM), but this platform has signific

115 ecipitation of COPII vesicles and immunogold electron microscopy (EM), we characterize the existence

116 lution ultrastructural images obtained using electron microscopy (EM).

117 ted Rad3-Rad26 heterotetrameric complex with electron microscopy enabled me to propose a structural m

118 were analyzed utilizing optical and scanning electron microscopy, encapsulation yield, particle size,

119 using focused-ion-beam assisted transmission electron microscopy (FIB-TEM) and validated by a numeric

120 ed plasma mass spectrometry and transmission electron microscopy for quantification and characterizat

121 Technical advances in cryo-electron microscopy have resulted in a series of atomic

122 with large-area Raman imaging, backscattered electron microscopy, histopathology, and microcomputed t

123 The Electron Microscopy Hole Punch (EMHP) is a streamlined s

124 M) and high-resolution scanning transmission electron microscopy (HR-STEM) indicate the formation of

125 haracterized by high resolution transmission electron microscopy (HRTEM), energy dispersive X-ray ana

126 e microstructural parameters of native gels, electron microscopy image analysis were performed and qu

127 We obtained 3-D electron microscopy images of podocytes and used quantit

128 d difference envelope density analysis, with electron microscopy imaging and computational modeling,

129 ve resolution and sensitivity for a range of electron microscopy imaging modalities, including, for e

130 ystallised graphitic layers, as confirmed by electron microscopy imaging, electron dispersive spectru

131 ge and mass spectrometry analyses as well as electron microscopy imaging.

132 Using confocal laser and scanning electron microscopy, immunofluorescence, and live-cell i

133 s were studied using analytical transmission electron microscopy in an attempt to answer this questio

134 g, fluorescence correlation spectroscopy and electron microscopy in live cells, we show that G12V K-R

135 sap and as nanoparticles under transmission electron microscopy in pores of intervessel pit membrane

136 BD-7B were characterized by a negative stain electron microscopy in the presence of ADP/MgCl2 Single-

137 hology, which we designate LAMP Transmission electron microscopy indicates that LAMP exhibits ACBC do

138 by atomic force microscopy and transmission electron microscopy, indicating that the self-assembled

139 Here, an in situ and ex situ electron microscopy investigation of structural evolutio

140 cidated at near-atomic resolution using cryo-electron microscopy, is strikingly similar to that obser

141 g aberration-corrected scanning transmission electron microscopy, it is found that the spontaneous po

142 , we employ in situ liquid-cell transmission electron microscopy (LCTEM) to directly observe the evol

143 Comparison with a 7.8 A resolution cryo-electron microscopy map of a Mediator-RNA polymerase II

144 A recently reported 9-A cryo-electron microscopy map of the Tetrahymena telomerase ho

145 tures of this segment determined by the cryo-electron microscopy method micro-electron diffraction ex

146 n-deuterium exchange mass spectrometry (MS), electron microscopy, mutagenesis, molecular dynamics sim

147 Furthermore, based on electron microscopy, neurons infected with VZV produced

148 ngle actin filaments that is consistent with electron microscopy observation.

149 ales in Scotland were processed for scanning electron microscopy observation.

150 Using dynamic, atomic-scale resolution electron microscopy observations and theory modelling, w

151 Operando scanning transmission electron microscopy observations of cathodic reactions i

152 Transmission electron microscopy of FECD tissues displayed an increas

153 Moreover, transmission electron microscopy of glomeruli and immunofluorescent s

154 rophages was also apparent from transmission electron microscopy of infected cells.

155 d, RNA-encapsidating nucleoprotein, and cryo-electron microscopy of nucleocapsid or nucleocapsid-like

156 pproaches originally developed for cryogenic electron microscopy of single particles.

157 t on the direct observation via transmission electron microscopy of the formation of bubble lattices

158 Serial block face scanning electron microscopy of zebrafish cones revealed that nea

159 of P. falciparum CSP, we used negative-stain electron microscopy on a recombinant shortened CSP (rsCS

160 scopy, Transmission (TEM) and Scanning (SEM) Electron Microscopy on Focused Ion Beam foils.

161 s that are not apparent through transmission electron microscopy or limited proteolysis.

162 Photon-induced near-field electron microscopy (PINEM) is a technique to produce an

163 ider the effect of photon-induced near-field electron microscopy (PINEM), first reported by Zewail et

164 using powder X-ray diffraction, transmission electron microscopy, Raman and wavelength/energy dispers

165 ctural characterizations (X-ray diffraction, electron microscopy, Raman, and UV-visible spectroscopie

166 bodies adjacent to a disorganized Z-line on electron microscopy, recapitulating the disease.

167 Here we used serial electron microscopy reconstructions to quantify polyribo

168 length as revealed by immunofluorescence and electron microscopy reflected cAMP-induced reorganizatio

169 egates that look amorphous and disordered by electron microscopy, reminiscent of the reported formati

170 axes of the V2O3; atomic force and scanning electron microscopy reveal oriented rips in the film mic

171 Transmission electron microscopy revealed abnormalities in the ultras

172 is of MMP-3 treated matrices by transmission electron microscopy revealed remodelling and degradation

173 Field emission scanning electron microscopy revealed that ethanol solutions of 3

174 Finally, electron microscopy revealed that Hrq1 and RecQ4 share s

175 ionally, immunohistochemistry and immunogold electron microscopy revealed that tibial marrow adipocyt

176 Atomic-resolution scanning transmission electron microscopy reveals an interesting local atomic

177 : see text]m(2) to [Formula: see text] cm(2) Electron microscopy reveals the excellent quality of the

178 Cryo-electron microscopy reveals the structure of a chloride

179 Scanning electron microscopy sampling showed a generally uniform

180 rm infrared spectrometry (FTIR) and scanning electron microscopy (SEM) and applied as a sorbent for s

181 Here we use scanning electron microscopy (SEM) and multiplex coherent anti-St

182 orphological characterizations with scanning electron microscopy (SEM) and transmission electron micr

183 Scanning Electron Microscopy (SEM) has been used to demonstrate s

184 rent morphology as was evident from scanning electron microscopy (SEM) imaging of their xerogels, XGh

185 y photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and in situ X-ray diffraction

186 phy (PET)/computed tomography (CT), scanning electron microscopy (SEM), and transition electron micro

187 of PES/AG membranes was studied by scanning electron microscopy (SEM), Raman spectroscopy, contact a

188 These nanostructures are studied by scanning electron microscopy (SEM), scanning transmission electro

189 anocomposite was characterised with scanning electron microscopy (SEM), transmission electron microsc

190 DX), atomic force microscopy (AFM), scanning electron microscopy (SEM), UV-Vis spectroscopy, X-ray di

191 on-optical methods (high-resolution scanning electron microscopy (SEM), wavelength-dispersive electro

192 f the bulk material was analyzed by Scanning Electron Microscopy (SEM), X-ray-tomography and Fourier-

193 owder X-ray diffraction (p-XRD) and scanning electron microscopy (SEM).

194 ssion electron microscopy (TEM) and scanning electron microscopy (SEM).

195 etween 2-8 mum can be observed from scanning electron microscopy (SEM).

196 e-collecting Ultra-Microtome (ATUM) Scanning Electron Microscopy (SEM).

197 hy/mass spectrometry (Py-GC/MS) and scanning electron microscopy (SEM).

198 ations to the surface of S. epidermidis, and electron microscopy showed cellular aggregates connected

199 Transmission electron microscopy showed that fibroblasts carrying the

200 Scanning electron microscopy showed that NaOH steeping produced m

201 Transmission electron microscopy shows a high density of single-cryst

202 Electron microscopy shows structural integrity of transf

203 evaluated using three orthogonal techniques: electron microscopy, single-particle inductively coupled

204 Round morphology (by transmission electron microscopy), size ( approximately 180 nm diamet

205 py and spectroscopy (STM/STS), photoemission electron microscopy/spectroscopy (PEEM) and mu-ARPES we

206 tron microscopy (SEM), scanning transmission electron microscopy (STEM) and energy dispersive X-ray s

207 nsity, as confirmed by scanning transmission electron microscopy (STEM) measurements.

208 scopy and liquid-phase scanning transmission electron microscopy (STEM) were used to quantitatively a

209 microscopy (AFM), and scanning transmission electron microscopy (STEM), we observe that devices with

210 ination of intact human gamma-secretase cryo-electron microscopy structure has opened the way for a d

211 er, comparison with a recently reported cryo-electron microscopy structure indicates that dramatic re

212 Here, we determine the cryo-electron microscopy structure of a central region of TPX

213 Here, we present a 2.9 A cryo-electron microscopy structure of a ribosome stalled duri

214 In a recent cryo-electron microscopy structure of chicken Slo2.2, the ion

215 Here, we report the cryo-electron microscopy structure of full-length ZntB from E

216 Here, we report the cryo-electron microscopy structure of mature Japanese encepha

217 Here we present the 3.0 angstrom cryo-electron microscopy structure of mTORC1 and the 3.4 angs

218 Here we present a cryo-electron microscopy structure of S. cerevisiae Hrd1 in c

219 A cryo-electron microscopy structure of Slo2.2 suggests that th

220 Here we report the cryo-electron microscopy structure of the assembled 1.4-mega

221 Here we report the cryo-electron microscopy structure of the native 100S ribosom

222 Here we report the cryo-electron microscopy structure of the peptide-activated G

223 We solved a 3.2 A cryo-electron microscopy structure of the Plasmodium falcipar

224 Here we report a cryo-electron microscopy structure of the postcatalytic P com

225 Here, we present the cryo-electron microscopy structure of the yeast SSU processom

226 vector transmission, we determined the cryo-electron microscopy structure of wild-type CNV in the na

227 Our 3.4-angstrom cryo-electron microscopy structure reveals how the adenosine

228 g a model substrate (casein), we report cryo-electron microscopy structures at near-atomic resolution

229 opy have resulted in a series of atomic cryo-electron microscopy structures of both human and yeast 2

230 Here we present cryo-electron microscopy structures of human TRPV6 in the ope

231 Here we present high-resolution cryo-electron microscopy structures of subtype B B41 SOSIP En

232 We present cryo-electron microscopy structures of the human HCN channel

233 Transmission electron microscopy studies demonstrate that single mole

234 Electron microscopy studies of peripheral lymphocytes an

235 ed out real-time atomic force microscopy and electron microscopy studies.

236 ng dynamic light scattering and transmission electron microscopy supports progesterone recognition le

237 While transmission electron microscopy (TEM) and operando X-ray absorption

238 rsive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and scanning electron microsco

239 tron probe microanalysis (EDX), transmission electron microscopy (TEM) combined with EDX, and micro-R

240 lar biology, immunostaining and transmission electron microscopy (TEM) methods, we studied DDQ's bene

241 address this challenge through transmission electron microscopy (TEM) of quartz nanopipets for SECM

242 U L3 XAS and transmission electron microscopy (TEM) reveal that initially sorbed U

243 Transmission electron microscopy (TEM) revealed that TFV and ADV-trea

244 le-particle-ICP-MS (sp-ICP-MS), Transmission Electron Microscopy (TEM), Analytical Ultracentrifugatio

245 Amyloid-assembly kinetics, transmission electron microscopy (TEM), and atomic force microscopy (

246 ning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy and X-ray

247 Using immuno-transmission electron microscopy (TEM), we observed that a large numb

248 of the SiNPs was evaluated with transmission electron microscopy (TEM).

249 sedimentation FFF or SdFFF) and transmission electron microscopy (TEM).

250 ng electron microscopy (SEM), and transition electron microscopy (TEM).

251 g electron microscopy (SEM) and transmission electron microscopy (TEM).

252 ndidate for specimen support of transmission electron microscopy (TEM).

253 le ultrathin sections imaged by transmission electron microscopy (TEM).

254 systems, optical microscopy and transmission electron microscopy, TEM) can only provide 2D simplifica

255 ated with the GJs are structures observed by electron microscopy termed the electrical synapse densit

256 ter chain activity analysis and transmission electron microscopy that demonstrate remarkable impairme

257 tering, intrinsic fluorescence, transmission electron microscopy, thioflavin-T binding, seeding, and

258 chniques, light microscopy, and transmission electron microscopy to characterize mutants of pollen-ex

259 super-resolution microscopy and transmission electron microscopy to determine the intracellular fate

260 Here, we have used cryo-electron microscopy to determine the structure of the 60

261 and annular dark-field scanning transmission electron microscopy to determine their lateral compositi

262 fluorescence, dynamic light scattering, and electron microscopy to elucidate how EGCG remodels Abeta

263 Here, we have used focused ion beam-scanning electron microscopy to generate 3D reconstructions of in

264 ese structures together with single-particle electron microscopy to generate three-dimensional models

265 e and demonstrate the vast potential of cryo-electron microscopy to guide the development of mefloqui

266 Here we use scanning ultrafast electron microscopy to image the dynamics of electrons a

267 unohistochemistry, neural tract tracing, and electron microscopy to investigate the origin and synapt

268 We used serial-section electron microscopy to reconstruct PNS neurons and their

269 force microscopy and environmental scanning electron microscopy to show that during fluid-rock inter

270 used conventional and two-photon imaging and electron microscopy to show that lysosomes traffic bidir

271 Here we employ high-resolution transmission electron microscopy to study vanadium oxide supported on

272 eeze-substituted alfalfa root cap cells with electron microscopy/tomography.

273 he transmembrane region of the original cryo-electron microscopy Torpedo model; the only pentameric l

274 characterized by photoluminescence, scanning electron microscopy, UV-Visible spectra and X-ray diffra

275 Furthermore, in transmission electron microscopy, vesicular structures are observed i

276 High resolution scanning electron microscopy was to quantify the size and distrib

277 Scanning transmission electron microscopy was used at sub-nanometric resolutio

278 Furthermore, scanning electron microscopy was used to investigate three filler

279 Using cryogenic electron microscopy, we analyzed the non-AAA structure o

280 Using cryo-electron microscopy, we characterize the architecture of

281 y with aggregation kinetics and transmission electron microscopy, we examined the effects of pH and i

282 Using light and electron microscopy, we found labeling for all three Nav

283 Using cryo-electron microscopy, we now visualize the functional mae

284 Using transmission electron microscopy, we observed that recombinant CrSEPT

285 performing in situ atomic-scale transmission electron microscopy, we report unusual room-temperature

286 Here, using in situ electron microscopy, we show how gold and silver nanocry

287 etic lineage-tracing and scanning-block face electron microscopy, we show that injury of sciatic nerv

288 Using cryo-electron microscopy, we show that the GroEL C-termini ma

289 ssays and immunofluorescent and transmission electron microscopy, we showed that S. pneumoniae rapidl

290 Using electron microscopy, we showed that this peptide physica

291 Using cryo-electron microscopy, we solved the atomic structure of a

292 ith YFP and serotonin antisera combined with electron microscopy were carried out on double-transgeni

293 ing and inhibition assays and negative stain electron microscopy were performed.

294 The complex was visualized by negative-stain electron microscopy, which revealed an architecture simi

295 mb with an image quality similar to scanning electron microscopy, while simultaneously visualizing in

296 was revealed by high-resolution transmission electron microscopy with dislocations being observed at

297 was examined by high resolution transmission electron microscopy with energy-dispersive X-ray spectro

298 cilitates the use of multi-electron beams in electron microscopy with higher current without compromi

299 ation of the particles included transmission electron microscopy, X-ray diffraction and asymmetrical

300 MoS2 QDs were characterized by transmission electron microscopy, X-ray diffraction, Raman spectrosco