ライフサイエンスコーパス: electron microscopy

1 with other experimental approaches like cryo-electron microscopy.

2 d pores and tunnels that were observed using electron microscopy.

3 rational circular dichroism, and optical and electron microscopy.

4 ty of metal ion distribution as confirmed by electron microscopy.

5 and atomic resolution scanning transmission electron microscopy.

6 atoms, as evident from X-ray diffraction and electron microscopy.

7 ng, targeted protein cross-linking, and cryo-electron microscopy.

8 th AT were compared with those from scanning electron microscopy.

9 tions by using in situ scanning transmission electron microscopy.

10 e two metals is monitored using transmission electron microscopy.

11 of Saccharomyces cerevisiae THO-Sub2 by cryo-electron microscopy.

12 resolution fluorescence and platinum replica electron microscopy.

13 should be used when identifying pathogens by electron microscopy.

14 ation-corrected high-resolution transmission electron microscopy.

15 ation of Golgi cisternae observed in earlier electron microscopy.

16 h-resolution structure determination by cryo-electron microscopy.

17 ditional imaging with cryogenic transmission electron microscopy.

18 rotron X-ray diffraction and high-resolution electron microscopy.

19 e of the C9orf72-SMCR8-WDR41 complex by cryo-electron microscopy.

20 sure freezing to examine their morphology by electron microscopy.

21 films were then examined using transmission electron microscopy.

22 oparticle tracking analysis and transmission electron microscopy.

23 cally resolved in-situ scanning transmission electron microscopy.

24 connections that were previously observed by electron microscopy.

25 r example with x-ray crystallography or cryo-electron microscopy.

26 d for the GA treatment based on transmission electron microscopy.

27 monary emboli using high-resolution scanning electron microscopy.

28 in treated samples were observed by scanning electron microscopy.

29 ture, at 2.6-angstrom resolution, using cryo-electron microscopy.

30 l laser spectral, confocal, and transmission electron microscopy.

31 metry, atomic force microscopy, and scanning electron microscopy.

32 lculated by using serial block-face scanning electron microscopy.

33 ultrathin series sectioning for transmission electron microscopy.

34 th hematologic neoplasms had substructure on electron microscopy.

35 a was generated by serial blockface scanning electron microscopy.

36 he information provided by visible light and electron microscopy.

37 tructural changes using single-particle cryo-electron microscopy.

38 ed by micro-computed tomography and scanning electron microscopy.

39 lly reconstituted in lipids optimal for cryo-electron microscopy.

40 ce topography was also viewed under scanning electron microscopy.

41 y correlated live-cell, super-resolution and electron microscopy.

42 nfrared spectroscopy, X-ray diffraction, and electron microscopy.

43 n and state-of-the-art scanning transmission electron microscopy.

44 Mitochondria were evaluated using electron microscopy.

45 sence and absence of hepcidin solved by cryo-electron microscopy.

46 teins have been studied in detail using cryo-electron microscopy(2,7,9-12), but the structure and dis

47 g aberration corrected scanning transmission electron microscopy (AC-STEM), UV-vis spectroscopy, and

48 Scanning electron microscopy analysis of the 3D EEC model reveale

49 Here we perform in situ transmission electron microscopy analysis of the synthesized red-phos

50 e active Hrd1 complex, as determined by cryo-electron microscopy analysis of two subcomplexes.

51 d dynamics and advanced in situ transmission electron microscopy analysis to elucidate the interplay

52 GNPs), via a combined hydrodynamic size and electron microscopy analysis.

53 red rats relate to mitochondrial morphology (electron microscopy and 3-dimensional reconstructions) a

54 cture and properties of ferritins using cryo-electron microscopy and a range of functional analyses i

55 nt components and analyzed its appearance by electron microscopy and ability to support histone pre-m

56 these two behaviors through a combination of electron microscopy and aggregation kinetics.

57 , and direct visualization with transmission electron microscopy and atomic force microscopy.

58 -resolved in-situ environmental transmission electron microscopy and atomistic simulation, we reveal

59 Scanning electron microscopy and colony forming unit counting are

60 At low concentration, transmission electron microscopy and dynamic light scattering identif

61 Using high-resolution transmission electron microscopy and electron energy-loss spectroscop

62 ray photoelectron spectroscopy, transmission electron microscopy and energy dispersive spectrometer c

63 Furthermore, correlative light-electron microscopy and energy-filtered transmission ele

64 Using cryo-electron microscopy and forcefield-based refinement, we

65 isolate complexed with antibodies using cryo-electron microscopy and harness this structural informat

66 mputed tomography followed by backscattering electron microscopy and histology.

67 om and 2.9 angstrom, respectively, with cryo-electron microscopy and image reconstruction methods.

68 ron X-ray tomography, light and transmission electron microscopy and in vivo ophthalmoscopy, we descr

69 bution using x-ray diffraction, transmission electron microscopy and in-situ small angle neutron scat

70 hroism spectra and the scanning transmission electron microscopy and optical microscope images shows

71 f plant CME as allowed by our advancement in electron microscopy and quantitative live imaging techni

72 oS(2) crystals, as confirmed by transmission electron microscopy and Raman signatures.

73 Electron microscopy and selected area diffraction measur

74 (ER) in cholangiocytes, but both immunogold electron microscopy and super-resolution microscopy show

75 data with the cell morphologies by scanning electron microscopy and the ion-concentration analysis b

76 ng thermal microscopy, scanning transmission electron microscopy and transition based threshold therm

77 ted Ric-8A at near atomic resolution by cryo-electron microscopy and X-ray crystallography.

78 RNAscope in situ hybridization, transmission electron microscopy, and confocal microscopy, we confirm

79 h wet-chemistry testing, optical microscopy, electron microscopy, and density functional theory, mole

80 cy Raman spectroscopy, scanning transmission electron microscopy, and electrical characterization.

81 by neutron activation analysis, transmission electron microscopy, and gas chromatography-mass spectro

82 Histology, scanning electron microscopy, and nanoindentation revealed hypomi

83 ere, we use chemical probes, single-particle electron microscopy, and native mass spectrometry to stu

84 oscopy, thermogravimetric analysis, scanning electron microscopy, and other spectroscopic techniques.

85 by Zeta potential, dynamic light scattering, electron microscopy, and other spectroscopic techniques.

86 tructions, stable isotope analysis, scanning electron microscopy, and sediment analyses, we document

87 se direct cilia electrophysiology, cryogenic electron microscopy, and superresolution imaging to dete

88 light scattering and environmental scanning electron microscopy, and with porcine mucin as the model

89 combined quantitative mass spectrometry/cryo-electron microscopy approach to detail the protein inven

90 Advances in cryo-electron microscopy are enabling increasingly elaborate

91 Optical and electron microscopies as well as electron and powder X-r

92 n, fluorescence, and analytical transmission electron microscopies as well as stable isotope labeling

93 nd O-acyltransferase (MBOAT) family, by cryo-electron microscopy at approximately 3.0 angstrom resolu

94 ion types of PIN clusters were determined by electron microscopy at the nanometer level at different

95 s operating in the infrared and highlight an electron-microscopy-based approach for probing complex-s

96 electron microscopy, combined with scanning electron microscopy, broadband femtosecond transient abs

97 Here, we demonstrate that cryo-electron microscopy can routinely resolve maps of RNA-on

98 Subsequently, we used correlative light electron microscopy (CLEM) to colocalize the RSV N prote

99 We used in situ high-resolution transmission electron microscopy combined with molecular dynamics sim

100 Electron microscopy combined with scanning mutagenesis i

101 re we applied cryogenic correlated light and electron microscopy, combined with electron cryo-tomogra

102 High-resolution cryogenic electron microscopy, combined with scanning electron mic

103 igned that achieves synchronous fluorescence-electron microscopy correlation.

104 micro-computed tomographic imaging, scanning electron microscopy, corrosion casting, and direct multi

105 Transmission electron microscopy coupled with energy dispersive X-ray

106 anning Raman spectroscopy (SRS) and scanning electron microscopy coupled with energy-dispersive X-ray

107 Using cryo-electron microscopy (cryo-EM) and biochemical approaches

108 Cryo-electron microscopy (cryo-EM) images show that new aggre

109 tarting from the recently reported cryogenic electron microscopy (cryo-EM) open-state channel structu

110 simulation results with the results of cryo-electron microscopy (cryo-EM) reconstruction of multiple

111 Cryo-electron microscopy (cryo-EM) showed that the design is

112 cally from experimental single-particle cryo-electron microscopy (cryo-EM) snapshots of ryanodine rec

113 Moreover, a 3.4 angstrom cryo-electron microscopy (cryo-EM) structure of a neutralizin

114 Here, we report the cryo-electron microscopy (cryo-EM) structure of Homo sapiens

115 Here, we present a cryo-electron microscopy (cryo-EM) structure of the Escherich

116 Here, we report cryo-electron microscopy (cryo-EM) structures of an intact Es

117 hell, we determined the high-resolution cryo-electron microscopy (cryo-EM) structures of cucumber lea

118 Here, we present cryo-electron microscopy (cryo-EM) structures of translationa

119 d molecular genetics, biochemistry, and cryo-electron microscopy (cryo-EM) to investigate the functio

120 Here, we use genetics and cryo-electron microscopy (cryo-EM) to study the high-resoluti

121 Using cryo-electron microscopy (cryo-EM), we determined the structu

122 Using single particle cryo-electron microscopy (cryo-EM), we report reconstructions

123 Data from a combination of cryo-electron microscopy (cryo-EM), x-ray crystallography, an

124 n, and determined their structure using cryo-electron microscopy (cryo-EM).

125 netic resonance (NMR) imaging, and cryogenic electron microscopy (cryo-EM).

126 Cryogenic transmission electron microscopy (cryo-TEM) revealed key differences

127 tube, and imaged with cryogenic transmission electron microscopy (cryo-TEM).

128 Cryo-electron microscopy (cryoEM) is becoming the preferred m

129 Here we report a cryo-electron microscopy (cryoEM) structure of PDE6 complexed

130 Our high-resolution cryo-electron microscopy (cryoEM) studies of B41 in complex w

131 sition and characterized them using scanning electron microscopy, cyclic voltammetry, and electrochem

132 collagen architecture, x-ray scattering and electron microscopy data were collected from paired WST-

133 Combining structural analyses of cryo-electron microscopy data with molecular dynamic simulati

134 has advanced greatly, particularly via cryo-electron microscopy data.

135 the lawn biofilms imaged using transmission electron microscopy demonstrate significant bacterial ce

136 Scanning electron microscopy demonstrated particle sizes of 3-100

137 Scanning and transmission electron microscopy demonstrates that metal enrichments

138 Field-emission scanning electron microscopy elucidated the morphology of the sub

139 relevance of the closed conformation, while electron microscopy (EM) and molecular dynamic (MD) simu

140 Here we present cryo-electron microscopy (EM) data resolving the EC1 and EC1+

141 The fast development of high-resolution electron microscopy (EM) demands a background-noise-free

142 3D can also display electron density maps or electron microscopy (EM) density maps, and export files

143 Complementary proteomics measurements and electron microscopy (EM) imaging are used to further cha

144 Electron microscopy (EM) of primary hepatocytes or hepat

145 CPSF and CstF and examined these factors by electron microscopy (EM).

146 d characterised by dynamic light scattering, electron microscopy, encapsulation efficiency, and drug

147 nt X-ray scattering and Lorentz transmission electron microscopy experiments.

148 characterised using field emission-scanning electron microscopy (FE-SEM) and cyclic voltammetry (CV)

149 Field Emission Gun-Scanning Single Electron Microscopy (FEG-SEM) revealed that treatment of

150 ction method using Focused Ion Beam/Scanning Electron Microscopy (FIB/SEM) can be applied to study in

151 Scanning electron microscopy for morphological characterization i

152 ron microscopy, high-resolution transmission electron microscopy, Fourier-transform infrared spectros

153 en adsorption/desorption isotherms, scanning electron microscopy, Fourier-transform infrared spectros

154 Recent advances in single-particle cryogenic electron microscopy have not only delivered crucial info

155 The catalysts were characterized by scanning electron microscopy, high-resolution transmission electr

156 We perform optical mapping and transmission electron microscopy in a drug-induced (sea anemone toxin

157 ray crystallography and single-particle cryo-electron microscopy in distinct conformational states, s

158 Using serial electron microscopy in the macaque retina, we reconstruc

159 Further, cryo-electron microscopy in the presence of Ca(2+) revealed t

160 Using correlative light and electron microscopy, in situ cryo-electron tomography, a

161 gle annular dark-field scanning transmission electron microscopy, in situ scanning Kelvin probe micro

162 autophagy events occurring upon injury using electron microscopy, in vivo tracking of autophagy marke

163 Furthermore, Lorentz transmission electron microscopy is used to directly image Neel-type

164 constructions of serial-section transmission electron microscopy, it was possible to reveal that the

165 Here, Liquid Phase Electron Microscopy (LPEM) captures the intermediate pre

166 Moreover, the cryo-electron microscopy map reveals that the C-edge of betaa

167 -lapse fluorescence microscopy, transmission electron microscopy, mathematical modelling and genetic

168 The in situ environmental transmission electron microscopy measurements herein show that pit fo

169 ed through a combination of scanning PTE and electron microscopy measurements of single-crystal and b

170 Here, we report the development of an electron microscopy method that combines serial block-fa

171 ate RGO aggregation as disclosed by scanning electron microscopy, most likely due to the electrostati

172 fetal meconium at mid-gestation by scanning electron microscopy (n = 4), and a sparse bacterial sign

173 ermination by X-ray crystallography and cryo-electron microscopy not only confirms that IrtAB has an

174 Using dynamic, atomic-scale electron microscopy observations and theoretical modelin

175 Immunofluorescence and electron microscopy of Drosophila tissues demonstrate an

176 Optical and electron microscopy of HIPK4-null male germ cells reveal

177 Focused ion-beam scanning electron microscopy of infected cells validated numerous

178 Electron microscopy of patient-derived lymphocytes and f

179 ervation, using energy-filtered transmission electron microscopy, of structural features attributable

180 into microstructured catalysts according to electron microscopy outcomes.

181 overall resolution of 3.4 angstroms by cryo-electron microscopy, permitting building of a nearly com

182 hybrid approach by performing new cryogenic electron microscopy reconstruction of myosin-S1-decorate

183 is of neutralization, we generated cryogenic electron microscopy reconstructions of Fab:CHIKV complex

184 The scanning electron microscopy results showed void spaces on the tr

185 microscopy and energy-filtered transmission electron microscopy reveal the well-associated optical a

186 itu analysis of particulates by transmission electron microscopy revealed 2-10 nm crystallites of fcc

187 ds, and whole-cell focused ion-beam scanning-electron microscopy revealed a deficiency of carotenoid-

188 Negative stain electron microscopy revealed a higher percentage of the

189 , immunofluorescence microscopy and scanning electron microscopy revealed temporal differences in adh

190 Aberration-corrected electron microscopy revealed that individual nanohelices

191 f the Macrotermes subhyalinus; with scanning electron microscopy revealing small spherical structures

192 on of p-MOFs was probed by cryo-transmission electron microscopy, revealing nonclassical pathways via

193 ex with a monoclonal antibody (mAb5) by cryo-electron microscopy, revealing the tertiary and quaterna

194 Further, electron microscopy reveals that plasma membrane "nanopo

195 Negative-stain electron microscopy reveals that the complex can adopt a

196 Aberration-corrected electron microscopy reveals that the nanoribbons are pre

197 aman and X-ray spectroscopy and transmission electron microscopy reveals the complete absence of long

198 Electron microscopy reveals unit disconnections in a low

199 We used a combination of cryo-electron microscopy, ribosome profiling, and mRNA stabil

200 ombination of light microscopy, transmission electron microscopy, RNA-Seq analyses and RNA in situ hy

201 Serial blockface scanning electron microscopy (SBSEM) is used to describe the sens

202 The combined use of scanning electron microscopy (SEM) and confocal laser scanning mi

203 ying atomic force microscopy (AFM), scanning electron microscopy (SEM) and electrochemical techniques

204 sform Infrared Spectroscopy (FTIR), scanning electron microscopy (SEM) as well as alamar blue, acridi

205 The Scanning electron microscopy (SEM) images demonstrated a relative

206 ) population using a combination of scanning electron microscopy (SEM) techniques.

207 m infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM), and energy-dispersive X-ray s

208 ng powder X-ray diffraction (pXRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX)

209 We demonstrate gas cluster ion beam scanning electron microscopy (SEM), in which wide-area ion millin

210 (FIB) system which, assembled with scanning electron microscopy (SEM), is the most popular tool used

211 aser particle diameter analyzer and scanning electron microscopy (SEM).

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

213 Atomic force microscopy and scanning electron microscopy show clusters and, occasionally, iso

214 However, electron microscopy showed heterogeneity in the particle

215 Also, ultrastructural examination by electron microscopy showed no evidence of viral particle

216 Assessment of the S protein trimer by cryo-electron microscopy showed that D614G disrupts an interp

217 anatomic data from confocal and transmission electron microscopy showing that single afferent fibers

218 Negative-stain electron microscopy shows that the essential CbbO adapto

219 Here we show through a series of cryo-electron microscopy single particle reconstructions how

220 By contrast, single-particle cryo-electron microscopy (SP-cryo-EM) routinely reaches near-

221 e tomography (APT) and scanning transmission electron microscopy (STEM) are currently the most suitab

222 pH conditions through scanning transmission electron microscopy (STEM) coupled with energy-dispersiv

223 actor-nucleosome interaction to empower cryo-electron microscopy structure determination of the compl

224 lations based on a recently solved cryogenic-electron microscopy structure of an active alpha(2)beta(

225 Here, we present the cryo-electron microscopy structure of an export gate containi

226 Here we present a cryo-electron microscopy structure of beta-arrestin 1 (betaar

227 A cryo-electron microscopy structure of the 16-helix transmembr

228 we determined a 3.5-angstrom-resolution cryo-electron microscopy structure of the 2019-nCoV S trimer

229 we report the first, to our knowledge, cryo-electron microscopy structure of the eukaryotic EMC.

230 Here, we provide the cryo-electron microscopy structure of the full-length WzmWzt

231 Here we present the high-resolution cryo electron microscopy structure of the GFLV-Nb23 complex,

232 Here we report the cryogenic electron microscopy structure of the neutral and basic a

233 e the coiled coil according to the cryogenic electron microscopy structure of TRPM8.

234 Using cryo-electron microscopy, structure-guided mutagenesis, and c

235 Here we determine cryogenic electron microscopy structures of ferroportin in lipid n

236 Here we report the cryo-electron microscopy structures of GPBAR-G(s) complexes s

237 Here, we present high-resolution cryo-electron microscopy structures of HIV intasomes bound to

238 Here we present two cryo-electron microscopy structures of human PAC in a high-pH

239 Here we describe multiple cryo-electron microscopy structures of human TRPV3 reconstitu

240 Here we report cryo-electron microscopy structures of influenza C virus poly

241 Here, we report the cryo-electron microscopy structures of murine SIgA and dIgA.

242 Here we solve the cryo-electron microscopy structures of NSD2 and NSD3 bound to

243 Cryo-electron microscopy structures of Saccharomyces cerevisi

244 Here we report cryo-electron microscopy structures of the DNA-binding domain

245 The cryo-electron microscopy structures of the EV71 virion in com

246 Here we present four cryo-electron microscopy structures of the human full-length

247 Using cryo-electron microscopy, structures for the p53 monomer (~50

248 Recent crystallography and electron microscopy studies have refined our model of he

249 has been in part due to misinterpretation of electron microscopy studies.

250 Characterization by scanning transmission electron microscopy suggests that when the catalyst is o

251 We also used FIB-SEM, a three-dimensional electron microscopy technique, to calculate the actual n

252 gment in detail using three-dimensional (3D) electron microscopy techniques and show they are tethere

253 Electron microscopy techniques are used to characterize

254 ion of microtubules by combining optical and electron microscopy techniques provides valuable informa

255 nalysis with X-ray diffraction, transmission electron microscopy (TEM) and energy dispersive X-ray sp

256 wder-X-ray diffraction (p-XRD), transmission electron microscopy (TEM) and scanning electron microsco

257 Transmission electron microscopy (TEM) images of these NP-exposed bac

258 s leading to neoplasia, we used transmission electron microscopy (TEM) on wing imaginal discs tempora

259 emineralized tissue sections by transmission electron microscopy (TEM) shows that GAG removal reduced

260 omic force microscopy (AFM) and transmission electron microscopy (TEM) were used to confirm the few-l

261 erol is routinely visualised by transmission electron microscopy (TEM), but higher-resolution tools a

262 cture (EXAFS) spectroscopy, and transmission electron microscopy (TEM), we also show that U(V) is gen

263 studied using atomic-resolution transmission electron microscopy (TEM).

264 techniques (Raman, UV-Vis) and transmission electron microscopy (TEM).

265 s of human and frog PANX1 determined by cryo-electron microscopy that revealed a heptameric channel a

266 using powder X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, inducti

267 overy after photobleaching, and transmission electron microscopy, this work investigates chromatin co

268 tructure determination and correlative light/electron microscopy, thus expanding the scope of cryogen

269 Here we used cryo-electron microscopy to elucidate the structure of an ago

270 We used light and electron microscopy to examine renal tissue for evidence

271 ed projections using anterograde tracers and electron microscopy to explore the maturation of this pa

272 We used single-particle cryo-electron microscopy to visualize the mode of action of t

273 upled with aberration-corrected transmission electron microscopy, to enable in situ imaging of the in

274 ction of the C4bC2 proconvertase obtained by electron microscopy together rationalize how hC4Nb8 prev

275 Advances in imaging methods such as electron microscopy, tomography, and other modalities ar

276 omes are in good agreement with current cryo-electron microscopy topology and consistent with long-th

277 Immunohistochemistry and transmission electron microscopy verified that PIM inhibitors promote

278 Three new studies use a whole adult brain electron microscopy volume to reveal new long-range conn

279 Leveraging a whole-brain electron microscopy volume, we studied the adult Drosoph

280 e human epidermis, in situ correlative light electron microscopy was performed on human skin biopsies

281 Using X-ray spectromicroscopy and electron microscopy we found that the co-aggregation of

282 es including super-resolution microscopy and electron microscopy we identified, in adult cardiac myoc

283 By means of siRNA-mediated transfection and electron microscopy we showed that moderate reduction in

284 RAG1 with methionine at residue 848 and cryo-electron microscopy, we determined structures that captu

285 y using in-situ high resolution transmission electron microscopy, we directly show a dual-step twinni

286 Using correlative light and electron microscopy, we further demonstrated that one of

287 Using biochemical approaches and cryo-electron microscopy, we have determined how three chroma

288 hniques with Raman spectroscopy and scanning electron microscopy, we investigated 10 papyri fragments

289 Using in situ transmission electron microscopy, we investigated the deposition and

290 Here, using cryo-electron microscopy, we show that alpha-synuclein inclus

291 id-state nuclear magnetic resonance and cryo-electron microscopy, we show that thiol groups of cystei

292 Users familiar with cryo-electron microscopy who get basic training in dual-beam

293 y mechanism is analyzed by cryo-transmission electron microscopy, wide-angle x-ray scattering, Fourie

294 These results were confirmed by transmission electron microscopy with energy dispersive X-ray detecti

295 By combining electron microscopy with glutamate immunogold labeling,

296 hod that combines serial block-face scanning electron microscopy with in situ hybridization (3D-EMISH

297 By utilizing focused ion beam-scanning electron microscopy with serial surface imaging, normall

298 d imaging techniques, including transmission electron microscopy with use of the negative stain or cr

299 pectroscopy mapping and in situ transmission electron microscopy within a sub-10 nm active device are

300 Scanning electron microscopy, X-ray photoelectron spectroscopy, t