ライフサイエンスコーパス: scanning electron microscopy

1 R spectroscopy, dynamic light scattering and scanning electron microscopy.

2 ng in grapevine (Vitis vinifera) paired with scanning electron microscopy.

3 in cell-surface topology were assessed using scanning electron microscopy.

4 sheep left ventricle using serial block face scanning electron microscopy.

5 osition of the nanocomposite was observed by scanning electron microscopy.

6 voxels collected by focused ion-beam milling scanning electron microscopy.

7 on with X-ray photoelectron spectroscopy and scanning electron microscopy.

8 l, as well as pyramidal, MN, as confirmed by scanning electron microscopy.

9 poly-Si nanowires for the first time, using scanning electron microscopy.

10 raphy as well as shortened enamel rods under scanning electron microscopy.

11 ray scattering, atomic force microscopy, and scanning electron microscopy.

12 ocopy, X-ray diffraction, and field emission scanning electron microscopy.

13 by X-ray diffraction, FT-IR spectroscopy and scanning electron microscopy.

14 illi and membrane folds, as determined using scanning electron microscopy.

15 ode tortuosity by using focused ion beam and scanning electron microscopy.

16 data with the ultrastructural resolution of scanning electron microscopy.

17 Disk surface morphology was evaluated by scanning electron microscopy.

18 which we visualized using serial block-face scanning electron microscopy.

19 rphology of the treated bacteria revealed by scanning electron microscopy.

20 erved and reconstructed by serial block face scanning electron microscopy.

21 reflected in the microstructural analysis by scanning electron microscopy.

22 vertebrae were harvested and evaluated with scanning electron microscopy.

23 Bud development was characterized using scanning electron microscopy.

24 n/removal was quantitated using confocal and scanning electron microscopy.

25 copy, second harmonic generation imaging and scanning electron microscopy, among other vital biologic

26 Scanning electron microscopy analysis confirmed the pres

27 Scanning electron microscopy analysis suggests that the

28 Our new quantitative technique combines scanning electron microscopy and 3D immunolocalization i

29 Scanning electron microscopy and atomic force microscopy

30 High resolution imaging methods (Scanning Electron Microscopy and Confocal Laser Scanning

31 Using scanning electron microscopy and confocal live imaging c

32 Scanning electron microscopy and cuticle staining confir

33 We present chemical (scanning electron microscopy and electron microprobe) an

34 Raman spectroscopy, scanning electron microscopy and energy dispersive spect

35 py, copper electrodeposits are visualized by scanning electron microscopy and energy dispersive spect

36 Scanning electron microscopy and energy dispersive spect

37 silicon, were found in great amounts by the Scanning electron microscopy and energy dispersive syste

38 bility were synthesized and characterized by scanning electron microscopy and energy dispersive X-ray

39 logy of the AIA particles were studied using scanning electron microscopy and energy-dispersive X-ray

40 The Ag/AgCl reference was characterized with scanning electron microscopy and energy-dispersive X-ray

41 Scanning electron microscopy and fluorescence image anal

42 Scanning electron microscopy and fluorescence microscopy

43 es of hyperiids (Crustacea; Amphipoda) using scanning electron microscopy and found two undocumented

44 Scanning electron microscopy and Fourier transform infra

45 ched in zinc were detected on whole cells by scanning electron microscopy and imaging mass spectromet

46 Scanning electron microscopy and immunochemistry were us

47 ous structures on CNF loading was studied by scanning electron microscopy and porosity measurement.

48 y immunofluorescence assays and confocal and scanning electron microscopy and quantified by quantitat

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

50 pitation polymerization and characterized by scanning electron microscopy and Scatchard analysis.

51 rase chain reaction, immunofluorescence, and scanning electron microscopy and showed similar patterns

52 Scanning electron microscopy and spectroscopic ellipsome

53 ted ceramic surfaces were characterized with scanning electron microscopy and surface roughness measu

54 ings is characterized by optical microscopy, scanning electron microscopy and tensile strength measur

55 Beads were characterised by scanning electron microscopy and thermal analysis using

56 m infrared spectroscopy, circular dichroism, scanning electron microscopy and transmission electron m

57 Fourier transmission infrared spectrometry, scanning electron microscopy and transmission electron m

58 d of nanoflakes that were characterized with scanning electron microscopy and transmission electron m

59 y diffraction, Raman spectra, field-emission scanning electron microscopy and transmission electron m

60 es (biofilm formation) on the IOL surface by scanning electron microscopy and ultrastructural capsula

61 ffraction, transmission electron microscopy, scanning electron microscopy and UV-Vis absorption spect

62 , we combine techniques in serial block-face scanning-electron microscopy and deep-learning-based ima

63 Scanning-electron microscopy and Raman spectroscopy allo

64 s retained better morphology (confirmed with scanning electron microscopy) and higher in vitro basal

65 yer was characterized by optical microscopy, scanning electron microscopy, and atomic force microscop

66 X-ray diffraction, Raman spectroscopy, scanning electron microscopy, and glow discharge spectro

67 nder defined conditions were investigated by scanning electron microscopy, and photophysical properti

68 ispersive x-ray spectroscopy, field emission scanning electron microscopy, and transmission electron

69 ectrode, identical location transmission and scanning electron microscopy, as well as X-ray absorptio

70 n pegs using a biofilm device and studied by scanning electron microscopy at 2, 5, and 10 days.

71 authors perform experiments using an in situ scanning electron microscopy based double cantilever bea

72 We perform experiments using an in situ scanning electron microscopy-based double cantilever bea

73 Atomic-force microscopy and scanning electron microscopy both revealed the smooth an

74 nverted to an uneven surface as confirmed by scanning electron microscopy, cohesiveness, consistency

75 Confocal and scanning electron microscopy confirm removal of biofilm

76 Fluorescence and scanning electron microscopy confirmed the presence of b

77 Using scanning electron microscopy, confocal microscopy, and c

78 Scanning electron microscopy coupled to energy dispersiv

79 been characterized by optical microscopy and Scanning Electron Microscopy coupled with Energy Dispers

80 The cryogenic-temperature scanning electron microscopy (cryo-SEM) was adopted to i

81 ospheres was evaluated using low temperature scanning electron microscopy (cryo-SEM).

82 Optical, confocal fluorescence and scanning electron microscopies demonstrated partial and

83 Results Scanning electron microscopy demonstrated nanopores in b

84 Scanning electron microscopy demonstrated significantly

85 Scanning electron microscopy demonstrated that the coati

86 Scanning electron microscopy documents ommatidial organi

87 cles (SiO2@PEI MPs) were characterized using scanning electron microscopy, dynamic light scattering,

88 operties, as revealed by Raman spectroscopy, scanning electron microscopy, electron microprobe analys

89 This study uses serial block-face scanning electron microscopy (EM) to collect two volumes

90 eatments were analyzed utilizing optical and scanning electron microscopy, encapsulation yield, parti

91 nction of position using optical microscopy, scanning electron microscopy, energy dispersive spectros

92 he fabricated electrode was characterized by scanning electron microscopy, energy-dispersive X-ray sp

93 Scanning electron microscopy, energy-dispersive X-ray sp

94 h PDQCM were characterized by field emission scanning electron microscopy, Energy-dispersive X-ray sp

95 nfirmed by X-ray photoelectron spectroscopy, scanning electron microscopy-energy dispersive X-ray ana

96 the remaining three animals were analyzed by scanning electron microscopy/energy dispersive spectrome

97 Finally, scanning electron microscopy/energy-dispersive X-ray ana

98 Bright-field and scanning electron microscopy established that coatings o

99 Field emission scanning electron microscopy (FE-SEM) and X-ray photoele

100 Furthermore, field emission scanning electron microscopy (FE-SEM) of benign and canc

101 Emmett-Teller (BET) analysis, field emission-scanning electron microscopy (FE-SEM), Fourier-transform

102 Field emission scanning electron microscopy (FE-SEM), X-ray diffraction

103 ed high-resolution imaging by field emission scanning electron microscopy (FESEM) with nanogold affin

104 es have been characterized by field emission scanning electron microscopy (FESEM), transmission elect

105 ntial UV-vis spectroscopy and field emission scanning electron microscopy (FESEM).

106 Focused ion beam scanning electron microscopy (FIB-SEM) and serial sectio

107 Focused Ion Beam Scanning Electron Microscopy (FIB-SEM) can automatically

108 hat a new imaging modality, focused ion beam scanning electron microscopy (FIB-SEM), can be used to g

109 ide correlation between light microscopy and scanning electron microscopy/FIB.

110 d for Si ion concentration determination and scanning electron microscopy for surface morphology anal

111 omposite was characterized by field emission scanning electron microscopy, Fourier transform infrared

112 enerative medicine; until now, histology and scanning electron microscopy have been the gold standard

113 diffraction, UV-vis absorption spectroscopy, scanning electron microscopy, high resolution transmissi

114 nt was analyzed by microcomputed tomography, scanning electron microscopy, histology, immunohistochem

115 The solution UV-vis spectra and scanning electron microscopy images of the electrodes sh

116 Scanning electron microscopy images of the fracture surf

117 The scanning electron microscopy images show that the averag

118 Scanning Electron Microscopy images shows that activated

119 Based on scanning electron microscopy images, we hypothesized tha

120 learning algorithms to segment biofilm from scanning electron microscopy images.

121 , can be investigated in three dimensions by scanning electron microscopy imaging of freshly created

122 Scanning electron microscopy imaging revealed that macro

123 Using confocal laser and scanning electron microscopy, immunofluorescence, and li

124 nd 7-wk-old mice were analyzed by histology, scanning electron microscopy, immunohistochemistry, and

125 measured by auditory brainstem responses and scanning electron microscopy in male Wistar rats.

126 s investigated here for the first time using scanning electron microscopy in order to document change

127 characterized with X-ray powder diffraction, scanning electron microscopy, inductively coupled plasma

128 r structure during digestion, as observed by scanning electron microscopy, light microscopy, and chan

129 ogy, immunohistochemistry, serial block-face-scanning electron microscopy, morphological reconstructi

130 Multi-beam scanning electron microscopy (mSEM) enables high-through

131 compared with results obtained previously by scanning electron microscopy, nuclear magnetic resonance

132 pilot whales in Scotland were processed for scanning electron microscopy observation.

133 Scanning electron microscopy observations revealed morph

134 Serial block face scanning electron microscopy of zebrafish cones revealed

135 According to scanning electron microscopy, partial penetration of pol

136 Scanning electron microscopy quantification of PD densit

137 highly correlated with pore area obtained by scanning electron microscopy (R(2) = 0.968).

138 d- and l-ascorbic acid were characterized by scanning electron microscopy, Raman spectroscopy and X-r

139 ke Mn3O4 was performed by X-ray diffraction, scanning electron microscopy, Raman spectroscopy, Brunau

140 terized by transmission electron microscopy, scanning electron microscopy, Raman spectroscopy, UV-vis

141 Combining the mu-CT observations with scanning electron microscopy resulted in a detailed unde

142 ystalline axes of the V2O3; atomic force and scanning electron microscopy reveal oriented rips in the

143 High-speed optical analysis and serial scanning electron microscopy reveal that the mechanical

144 Scanning electron microscopy revealed a highly porous st

145 Scanning electron microscopy revealed distinct surface u

146 Cryo-scanning electron microscopy revealed gradual increases

147 Scanning electron microscopy revealed hollow needle-shap

148 localization to the flagellar membrane, and scanning electron microscopy revealed more intense TbHrg

149 Time-lapse imaging and scanning electron microscopy revealed that APYS1 caused

150 Scanning electron microscopy revealed that carbonate min

151 Scanning electron microscopy revealed that during tomato

152 Field emission scanning electron microscopy revealed that ethanol solut

153 X-ray photoelectron spectroscopy and scanning electron microscopy revealed that the nitrated

154 Scanning electron microscopy revealed that the synthesis

155 METHODS AND Scanning electron microscopy revealed that the synthesis

156 Scanning electron microscopy revealed that the therapeut

157 Scanning electron microscopy reveals marked differences

158 Anatomical analysis using scanning electron microscopy reveals that the eyes of Tu

159 Scanning electron microscopy reveals the interconnected

160 s such as in situ pressure and gas analyses, scanning electron microscopy, rotating disk electrode vo

161 Scanning electron microscopy sampling showed a generally

162 Bulk chemical analysis, scanning electron microscopy, secondary ion mass spectro

163 Scanning electron microscopy (SEM) analysis shows that t

164 In this study, besides wet chemistry and scanning electron microscopy (SEM) analysis, a Fourier-t

165 stub, and sputter-coated with a Au layer for scanning electron microscopy (SEM) analysis.

166 Scanning electron microscopy (SEM) and AFM imaging of C.

167 r transform infrared spectrometry (FTIR) and scanning electron microscopy (SEM) and applied as a sorb

168 ge of the cell surfaces was also revealed by scanning electron microscopy (SEM) and atomic force micr

169 Morphological analyses of GMs by scanning electron microscopy (SEM) and atomic force micr

170 The MD results agree well with scanning electron microscopy (SEM) and electrochemical i

171 composite of RuNPs-CNTs was characterized by scanning electron microscopy (SEM) and energy dispersive

172 les include powder X-ray diffraction (pXRD), scanning electron microscopy (SEM) and Fe 2p X-ray photo

173 ier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM) and gas chromatograph

174 oil after primary drainage was observed with Scanning Electron Microscopy (SEM) and identified using

175 Here we use scanning electron microscopy (SEM) and multiplex coheren

176 the nanocomposite film was characterized by scanning electron microscopy (SEM) and profilometry.

177 tigated by means of X-Ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spectroscop

178 Enzyme immobilization is confirmed by Scanning Electron Microscopy (SEM) and Raman Spectroscop

179 ve solid deposits which could be observed by scanning electron microscopy (SEM) and Raman spectroscop

180 es of different scales were determined using scanning electron microscopy (SEM) and scanning electron

181 kinetic studies by absorption spectroscopy, scanning electron microscopy (SEM) and scanning transmis

182 X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission elec

183 Scanning electron microscopy (SEM) and transmission elec

184 of the primary M7C3 carbide are observed by scanning electron microscopy (SEM) and transmission elec

185 well as morphological characterizations with scanning electron microscopy (SEM) and transmission elec

186 structure of the hybrid was characterized by scanning electron microscopy (SEM) and transmission elec

187 racterized by atomic force microscopy (AFM), scanning electron microscopy (SEM) and X-ray diffraction

188 Atomic force microscopy (AFM) and scanning electron microscopy (SEM) confirmed the size, s

189 zing the results of Cyclic Voltammetry (CV), Scanning Electron Microscopy (SEM) Electrochemical Imped

190 Scanning Electron Microscopy (SEM) has been used to demo

191 n electron microscopy (TEM) and conventional scanning electron microscopy (SEM) have been routinely u

192 ynchrotron X-ray microdiffraction (SXRD) and scanning electron microscopy (SEM) have been used to mea

193 Scanning electron microscopy (SEM) images provide insigh

194 r scaffolds was validated from multi-view 2D scanning electron microscopy (SEM) images.

195 ave different morphology as was evident from scanning electron microscopy (SEM) imaging of their xero

196 Fluorescent labeling and scanning electron microscopy (SEM) imaging show that dir

197 Scanning electron microscopy (SEM) imaging showed a non-

198 osomes, membrane depolarization studies, and scanning electron microscopy (SEM) in living bacteria.

199 ctroscopy (EIS), X-ray diffraction (XRD) and scanning electron microscopy (SEM) measurements.

200 Miyake-Apple imaging and scanning electron microscopy (SEM) of PPC were conducted

201 Brunauer-Emmett-Teller (BET) and scanning electron microscopy (SEM) results indicate that

202 Surface morphologies examined using scanning electron microscopy (SEM) showed characteristic

203 situ during the CO2 reduction reaction, and scanning electron microscopy (SEM) shows the surface to

204 The units were examined by scanning electron microscopy (SEM) under three condition

205 Scanning electron microscopy (SEM) was used for surface

206 r transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) were also used to eva

207 also identified by electrochemical methods, scanning electron microscopy (SEM), and atomic force mic

208 lectrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and electron dispers

209 X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersiv

210 with X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and in situ X-ray di

211 d by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and powder X-ray dif

212 he morphological changes, as demonstrated by scanning electron microscopy (SEM), and providing protec

213 rier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and spectrofluorimet

214 gy of the obtained films was investigated by scanning electron microscopy (SEM), and the formation of

215 n tomography (PET)/computed tomography (CT), scanning electron microscopy (SEM), and transition elect

216 sing transmission electron microscopy (TEM), scanning electron microscopy (SEM), atomic force microsc

217 impedance spectroscopy (EIS), ellipsometry, scanning electron microscopy (SEM), atomic force microsc

218 IS), X-ray diffraction (XRD), contact angle, scanning electron microscopy (SEM), atomic force microsc

219 characterized by infrared spectroscopy (IR), scanning electron microscopy (SEM), electrochemical impe

220 Scanning electron microscopy (SEM), electron microprobe

221 All samples were characterized by the scanning electron microscopy (SEM), Fourier transform in

222 Cell growth and behaviour was assessed by scanning electron microscopy (SEM), immunofluorescence m

223 matically characterized using field emission scanning electron microscopy (SEM), Raman spectra, Fouri

224 roperties of PES/AG membranes was studied by scanning electron microscopy (SEM), Raman spectroscopy,

225 These nanostructures are studied by scanning electron microscopy (SEM), scanning transmissio

226 rier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), SEM-energy dispersiv

227 The microcapsulates were characterized by scanning electron microscopy (SEM), thermal analysis (TG

228 ly characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electro

229 of GO and Al2O3 and characterized using the scanning electron microscopy (SEM), transmission electro

230 terization of samples were carried out using scanning electron microscopy (SEM), transmission electro

231 re studied by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electro

232 ode surface has been carried out by means of scanning electron microscopy (SEM), transmission electro

233 echniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electro

234 lysis (NTA), or electron microscopy imaging (scanning electron microscopy (SEM), transmission electro

235 c oxide nanocomposite was characterised with scanning electron microscopy (SEM), transmission electro

236 Scanning electron microscopy (SEM), transmission electro

237 alysis (EDX), atomic force microscopy (AFM), scanning electron microscopy (SEM), UV-Vis spectroscopy,

238 us electron-optical methods (high-resolution scanning electron microscopy (SEM), wavelength-dispersiv

239 d by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (X

240 rmation of the bulk material was analyzed by Scanning Electron Microscopy (SEM), X-ray-tomography and

241 transmission electronic microscopy (TEM) and scanning electron microscopy (SEM).

242 omatography/mass spectrometry (Py-GC/MS) and scanning electron microscopy (SEM).

243 e lying between 2-8 mum can be observed from scanning electron microscopy (SEM).

244 are ~240-360 in total number as estimated by scanning electron microscopy (SEM).

245 onfocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM).

246 inear sweep stripping voltammetry (LSSV) and scanning electron microscopy (SEM).

247 d using powder X-ray diffraction (p-XRD) and scanning electron microscopy (SEM).

248 , transmission electron microscopy (TEM) and scanning electron microscopy (SEM).

249 ere analyzed using light microscopy (LM) and scanning electron microscopy (SEM).

250 Differential Scanning Calorimetry (DSC), and Scanning Electron Microscopy (SEM).

251 (4-probe STM) under real-time monitoring of scanning electron microscopy (SEM).

252 in high-resolution images, for example, via scanning electron microscopy (SEM).

253 mated Tape-collecting Ultra-Microtome (ATUM) Scanning Electron Microscopy (SEM).

254 All capsulotomy specimens were collected for scanning electron microscopy (SEM).

255 croscopy, atomic-force microscopy (AFM), and scanning electron microscopy (SEM).

256 Also, scanning electron microscopy showed an interaction betwe

257 While ingestion of fibers was not observed, scanning electron microscopy showed carapace and antenna

258 Scanning electron microscopy showed that 2D6 IgA promote

259 ation performed by both light microscopy and scanning electron microscopy showed that antifungal acti

260 Scanning electron microscopy showed that NaOH steeping p

261 Scanning electron microscopy shows that aligned CNTs are

262 A scanning electron microscopy study revealed the spherica

263 8% of IOL optic surfaces (n = 13) studied by scanning electron microscopy, suggesting the presence of

264 Autoradiography and focused ion beam/scanning electron microscopy techniques were used to cha

265 Fourier transform infrared spectroscopy and scanning electron microscopy techniques.

266 nswells within 1-2 weeks by transmission and scanning electron microscopy (TEM and SEM, respectively)

267 swelling and gluten network, as evidenced by scanning electron microscopy, therefore BO pasta had str

268 eruli in the antennal lobe in the brain, and scanning electron microscopy to compare length and numbe

269 SC) with three-dimensional serial block-face scanning electron microscopy to determine the distributi

270 Here, we have used focused ion beam-scanning electron microscopy to generate 3D reconstructi

271 We employed serial block face-scanning electron microscopy to investigate Alport syndr

272 re we show a non-destructive technique using scanning electron microscopy to map buried junction prop

273 Here we used serial block-face scanning electron microscopy to obtain 3D volume measure

274 growth and etching experiments with in situ scanning electron microscopy to reveal the stacking sequ

275 se atomic force microscopy and environmental scanning electron microscopy to show that during fluid-r

276 We used high-through-put serial block-face scanning-electron-microscopy to reconstruct the network

277 is absorption and fluorescence spectroscopy, scanning electron microscopy, transmission electron micr

278 ctural characterization using field emission scanning electron microscopy, transmission electron micr

279 Scanning electron microscopy, transmission electron micr

280 rent techniques including X-ray diffraction, scanning electron microscopy, transmission electron micr

281 d, were characterized using transmission and scanning electron microscopy, ultra violet-visible and X

282 res were characterized by photoluminescence, scanning electron microscopy, UV-Visible spectra and X-r

283 High resolution scanning electron microscopy was to quantify the size an

284 Furthermore, scanning electron microscopy was used to investigate thr

285 Here, using microcomputed tomography and scanning electron microscopy, we compared the size and e

286 Also by volume scanning electron microscopy, we confirmed the presence

287 n depletion microscopy and serial block-face scanning electron microscopy, we defined ER accumulation

288 e size, dry dispersion particle analysis and scanning electron microscopy, we show that xyloglucan is

289 confocal laser scanning microscopy and cryo-scanning electron microscopy were coupled with textural

290 used correlative light and serial block-face scanning electron microscopy, which we term 3D-CLEM, to

291 bers are atomic force microscopy imaging and scanning electron microscopy, which well characterize su

292 of the limb with an image quality similar to scanning electron microscopy, while simultaneously visua

293 ssion electron microscopy and focal ion beam-scanning electron microscopy with Annexin V immunogold-l

294 samplers and analyzed by computer-controlled scanning electron microscopy with energy dispersive X-ra

295 using scanning electron microscopy (SEM) and scanning electron microscopy with energy dispersive X-ra

296 r 2008) were analyzed by computer-controlled scanning electron microscopy with energy dispersive X-ra

297 Combining scanning electron microscopy with energy dispersive X-ra

298 Scanning electron microscopy with energy-dispersive X-ra

299 amined by single-particle mass spectrometry, scanning electron microscopy with energy-dispersive X-ra

300 f 5-6 nm is confirmed by Raman spectroscopy, scanning electron microscopy, X-ray photoelectron spectr