ライフサイエンスコーパス: SEM

1 SEM analysis of the films indicates a good material comp

2 SEM and Raman spectroscopy were used to demonstrate that

3 SEM and XPS analysis are employed to characterize the el

4 SEM elemental mapping of samples taken from both swatche

5 SEM examination for control and CNTs specimens showed th

6 SEM imagery, skeletal trace elements and boron isotopes

7 SEM images of early biominerals from Ediacaran and Cambr

8 SEM images of hydrolyzed macroalgae showed that reverse-

9 SEM images revealed damaged starch granules after size r

10 SEM models with maximum-likelihood estimates made use of

11 SEM revealed capsule formation with entrapped catechin,

12 SEM revealed shellac-based coatings to contain spherical

13 SEM reveals that the cuticle consists of nanostructures

14 SEM showed clear empty cavities in the plain Ca-alginate

15 SEM studies revealed that MN58b distorted the cell wall,

16 SEM with energy-dispersive X-ray spectroscopy analysis d

17 SEM/EDS revealed characteristic surface weathering on th

18 forced expiratory volume in 1s (FEV(1) ) +/- SEM = 0.9 +/- 0.1 l, 30% of predicted) and eight control

19 0.35 +/- 0.13 SEM and kappa = 0.38 +/- 0.11 SEM) and moderate (kappa = 0.52 +/- 0.13 SEM).

20 s ranges between fair (kappa = 0.35 +/- 0.13 SEM and kappa = 0.38 +/- 0.11 SEM) and moderate (kappa =

21 .11 SEM) and moderate (kappa = 0.52 +/- 0.13 SEM).

22 ws moderate agreement (kappa = 0.48 +/- 0.14 SEM) with the consensus reading.

23 ck-traced anatomical LMN counts (336 +/- 16 [SEM]).

24 ate (22.5 +/- 3.1 compared with 47.2 +/- 7.3 SEM umol/g) coincided with significantly higher concentr

25 om forelimb wrist flexor muscles (415 +/- 8 [SEM]) align with back-traced anatomical LMN counts (336

26 In addition, SEM and AFM images illustrated a completely non-uniform

27 Additionally, SEM confirmed that most of Pb and Cd nanoparticles (NPs)

28 Additionally, SEM observations revealed good contact of CTCs with Si N

29 The texture analysis and SEM further validated structural maintenance.

30 tologic architecture preservation on H&E and SEM as well as preservation of key proteins such as coll

31 anism was investigated through FTIR, EDX and SEM, which demonstrated that the introduction of thiol g

32 at each step were characterized by FTIR and SEM.

33 y fluorescence spectroscopy, micro-FTIR, and SEM-EDS.

34 Integration of multi-trait models-GWAS and SEM-GWAS identified six significant SNPs for SCS, and qu

35 on scanning electron microscopy (HRSEM), and SEM with energy dispersive X-ray spectroscopy (SEM-EDS).

36 eJ to measure changes in pixel intensity and SEM-EDS for compositional analysis.

37 e method and characterized by XRD, FT-IR and SEM.

38 The NPN assay, electrolytic leakage and SEM analysis showed membrane damage in bacterial cells.

39 on for quantification of the morphology; and SEM-EDS was utilized to locate the impurity within the a

40 ons (C, H, N, O, S), Py-GC/FID, Py-GC/MS and SEM imaging reveal extensive degradation of the wood pol

41 SDS-PAGE and SEM analyses were also carried out to compare extraction

42 ng a wavelength dispersive spectrometer) and SEM-EDS (scanning electron microscopy analysis using an

43 ese polymers using DSC, FT-IR, XRD, TGA, and SEM techniques demonstrate consistency with the degree o

44 ogical changes were characterised by XRD and SEM.

45 Incorporating gas cluster ion beam SEM into existing single-beam and multibeam SEM workflow

46 phases identified by CT and by invasive BSE-SEM is demonstrated.

47 L (Ne-TML) was prepared and characterised by SEM, XRD and FTIR.

48 Q, as template molecule and characterized by SEM and FT-IR.

49 The sorbent was characterized by SEM, XRD, EDS, and FT-IR.

50 helated cell lysate complex was confirmed by SEM and Energy Dispersive X-ray Spectrometry (EDX).

51 ative to DES, which was further confirmed by SEM and TEM.

52 crostructure of the samples was evaluated by SEM microscopy, sugars content by HPLC and sucrose melti

53 ies of hot-pressed ZrC(1-x) were examined by SEM, XRD, Raman spectroscopy and static (13)C NMR spectr

54 the ultrastructure of the flour and fiber by SEM and particle size distribution.

55 ture of the FSPS samples was investigated by SEM and TEM imaging, and the observations were used to g

56 and spherical morphologies were observed by SEM and characterized by FTIR.

57 s and rough structure matrix was observed by SEM of the freeze-dried powdered sample.

58 and no obvious effect in Yunnan province by SEM.

59 by digitally "stitching" together contiguous SEM images.

60 , EXAFS) and nanoscale analysis (correlative SEM and nanoSIMS) that organic carbon is bound to reacti

61 Cryo-SEM results further showed a decrease in particle size a

62 amined using X-ray micro-tomography and cryo-SEM.

63 n by cryo-scanning electron microscopy (Cryo-SEM) analysis.

64 cryogenic-scanning electron microscopy (cryo-SEM), confocal laser scanning microscopy and laser diffr

65 We used cryo-SEM, fluorescence lifetime imaging microscopy (FLIM), au

66 thickness (least-squares mean difference +/- SEM: -0.9+/-0.4 mm, P=0.017), interventricular septal wa

67 crease in a murine NSG model of disseminated SEM cell-derived ALL, wherein CD19+ cells closely associ

68 wed a more organized and dense morphology (E-SEM), higher water vapor barrier, better mechanical feat

69 such tips is hard to characterize by either SEM or atomic force microscopy (AFM) that has been emplo

70 d sensor were assessed by scanning electron (SEM) and atomic force microscopy (AFM), electrochemical

71 Hill-Climbing algorithm was used to estimate SEM parameters.

72 ER profiles identified in serial block-face SEM images.

73 FE-SEM reliably resolved sorghum protein body structure, al

74 FE-SEM, but not pepsin assay, reliably detects HD nutation

75 onto nanocomposite was confirmed by AFM, FE-SEM, FTIR, and CLSM.

76 It was characterized using FTIR, FE-SEM/EDX before and after analyte ions biosorption.

77 ld-emission scanning electron microscope (FE-SEM) and high-resolution transmission electron microscop

78 ld emission scanning electron microscope (FE-SEM), and transmission electron microscope (TEM) with ED

79 ld emission scanning electron microscope (FE-SEM, SEM-Mapping), scanning transmission electron micros

80 ld emission-scanning electron microscopy (FE-SEM) and cyclic voltammetry (CV).

81 ution field emission electron microscopy (FE-SEM) method to detect the mutation (HD) in hard-endosper

82 ld emission scanning electron microscopy (FE-SEM) were used.

83 ld emission-scanning electron microscopy (FE-SEM), and Fourier-transform infrared spectroscopy (FT-IR

84 ith energy dispersive X-ray spectroscopy (FE-SEM/EDS) and Brunauer-Emmett-Teller (BET) analysis.

85 ed on FTIR, XPS, XRD, Raman spectroscopy, FE-SEM, HR-TEM, AFM, UV-Vis and FL, revealed successful dop

86 duced biosensor was characterized by XRD, FE-SEM, EDS, FT-IR and differential pulse voltammetry.

87 ed extensively using TEM, EDX, SAED, XRD, FE-SEM, FTIR, DIC, and electrochemical techniques.

88 vement region of the frontal eye fields (FEF(SEM)) is a critical node in the neural circuit controlli

89 preparatory modulation of firing rate in FEF(SEM) predicts movement, providing evidence against the '

90 eparatory activity evolves in the monkey FEF(SEM) during fixation in parallel with an objective measu

91 We propose that the use of FEF(SEM) output as a gain signal rather than a movement comm

92 ly, there is a partial reorganization of FEF(SEM) population activity between preparation and movemen

93 Gun-Scanning Single Electron Microscopy (FEG-SEM) revealed that treatment of the beta-amino HMOs sign

94 Here, we use correlative FIB-SEM, light- and cryo-electron microscopy approaches to e

95 tor incorporated into a commercial Ga(+) FIB-SEM (Focused Ion Beam combined with Scanning Electron Mi

96 Immunogold FIB-SEM offers the potential for broad applicability to corr

97 Here, immunogold FIB-SEM, which combines antigen labeling with in situ FIB-SE

98 d ion beam scanning electron microscopy (FIB-SEM) has provided unparalleled insight through the volum

99 d ion beam scanning electron microscopy (FIB-SEM) in conjunction with high-pressure freezing, freeze-

100 d ion beam-scanning electron microscopy (FIB-SEM) nano-tomography image dataset was used to reconstru

101 d ion beam-scanning electron microscopy (FIB-SEM) nano-tomography.

102 d ion beam scanning electron microscopy (FIB-SEM) to study the architecture of the pronuclear membran

103 n beam and scanning electron microscopy (FIB-SEM).

104 d ion beam-scanning electron microscopy (FIB-SEM); myelin outfoldings were three-dimensionally recons

105 h combines antigen labeling with in situ FIB-SEM imaging, is developed in order to spatially map ultr

106 ive cell imaging in mouse kidney tissue, FIB-SEM, and other complementary techniques, we provide new

107 Given that it is impractical to use FIB-SEM brain-wide, we used previously available SDM data fr

108 We also used FIB-SEM, a three-dimensional electron microscopy technique,

109 hree-dimensional densities obtained with FIB-SEM (synapses/um(3)) and the bi-dimensional densities ob

110 d Ion Beam/Scanning Electron Microscopy (FIB/SEM) can be applied to study in detail the synaptic orga

111 of wine PR proteins by up to 57% and 37% for SEM and SAB, respectively, and reduced the amount of haz

112 Remaining bacteria were quantified from SEM images of the implant surfaces and their numbers sta

113 Man-AOP was characterized by FTIR, SEM and PXRD revealing a covalent interaction.

114 Genomic SEM can be used to model multivariate genetic associatio

115 Genomic SEM is flexible and open ended, and allows for continuou

116 Genomic SEM synthesizes genetic correlations and single-nucleoti

117 Polygenic scores from genomic SEM consistently outperform those from univariate GWASs.

118 nomic structural equation modelling (genomic SEM): a multivariate method for analysing the joint gene

119 demonstrate several applications of genomic SEM, including a joint analysis of summary statistics fr

120 In SEM cells, CTCF loss notably disrupted intra-TAD loops a

121 ity, smooth surface and low agglomeration in SEM.

122 bio-MSPE sorbent were investigated by FT-IR, SEM, and EDX.

123 o gold nanoparticle, characterized by FT-IR, SEM, cyclic voltammetry and gel electrophoresis.

124 locus in a human pediatric B-ALL cell line, SEM, and an immortal erythroid precursor cell line, HUDE

125 High magnification SEM images show that the thin film is comprised of a net

126 The mean+/-standard error of the mean (SEM) VAS pain scores immediately after intravitreal inje

127 TcVI discrete typing units, with a mean (+/-SEM) of 3.9 +/- 0.7 haplotypes/patient, and 47% harbored

128 Mean +/- SEM cumulative urinary d6-alpha-CEHC derived from the in

129 Mean +/- SEM LDL-cholesterol concentrations (109.9 +/- 4.5 compar

130 Mean +/- SEM pre- and postfilter venous plasma glucose concentrat

131 Mean +/- SEM TMAO concentrations were significantly lower overall

132 UC 0.81 +/- 0.01 vs. 0.73 +/- 0.02, mean +/- SEM, comparison p = 0.002), with a mean classification a

133 +92 +/- 57 muU/timepoint p = 0.03; mean +/- SEM), but not for lactate (-0.14 +/- 0.04 mM/timepoint v

134 assification accuracy of 73 +/- 1% (mean +/- SEM) for M- and 69 +/- 1% for beta-based models.

135 : 17 +/- 10; 37 +/- 10; 30 +/- 10) (mean +/- SEM BOS, stable, control, respectively) (P < 0.05 for al

136 0% fat intervention was 55% +/- 3% (mean +/- SEM; n = 10), which was 9% less than during the 0% fat i

137 after CR, 2gOBG, 4gOBG, and 4gloMW (mean +/- SEM: 887 +/- 64, 831 +/- 61, 834 +/- 78, and 847 +/- 68

138 tion: weighed intake increased by a mean +/- SEM of 143 +/- 21 g/d (16%) and energy intake increased

139 In study 1, participants ate (mean +/- SEM) 42 +/- 15 g less in the slow- than in the fast-ER c

140 ed with metastatic prostate cancer (mean +/- SEM = 21 +/- 2.957 CTCs/mL, median = 21 CTCs/mL), demons

141 of the Bifidobacterium genus from (mean +/- SEM) 5.3% +/- 5.9% to 18.7% +/- 15.0%.

142 g fat-free mass was reduced in IMB (mean +/- SEM: -3.6% +/- 0.5%; P = 0.030) but not CTL with no diff

143 markedly smaller in CT individuals (mean +/- SEM: 2174 +/- 142 mum 2) compared with controls (3586 +/

144 Sixteen healthy males (mean +/- SEM age: 23 +/- 1 y) underwent 7 d of unilateral lower-l

145 lthy, young, endurance-trained men (mean +/- SEM age: 27 +/- 1 y) received a primed continuous infusi

146 Fifty-four participants (57.4% men; mean +/- SEM age: 52 +/- 3 y; BMI: 25.8 +/- 0.5 kg/m2) completed

147 Overall, (mean +/- SEM) patellar, tibial, and femoral cartilage T1rho relax

148 tion of 0, 15, 30, or 45 g protein (mean +/- SEM: -0.31+/- 0.16, 5.08 +/- 0.21, 10.04 +/- 0.30, and 1

149 y protein turnover with a resultant mean +/- SEM 0.03 +/- 0.01 mumol . kg LBM-1 . min-1 lower net bal

150 Twelve subjects (mean +/- SEM, 42 +/- 2 years, body mass index 37.4 +/- 1.2 kg/m(2

151 lic or diastolic BP (n = 6,554; the mean +/- SEM change in BP associated with a 100-mg difference in

152 The mean +/- SEM plasma protein fractional synthesis rate was 0.13 +/

153 and women (n = 89; 21.6 +/- 0.23 y; mean +/- SEM) were randomly allocated into 1 of 3 supplement grou

154 Mean+/-SEM pain scores 4 hours after injection were 1.6 +/- 0.4

155 Total mean+/-SEM procedure time was 124 +/- 5 seconds for patients tr

156 Data are presented as means +/- SEMs.

157 rotected N-[2-(trimethylsilyl)ethoxy]methyl (SEM) arylboronate ester precursor in a 17% +/- 5% (n = 1

158 rs followed by scanning electron microscope (SEM) analysis immediately or after rinsing with 0.9% NaC

159 iment inside a scanning electron microscope (SEM) chamber.

160 dsorption, and scanning electron microscope (SEM) data.

161 model based on scanning electron microscope (SEM) images of our substrates to explain our experimenta

162 cope (AFM) and scanning electron microscope (SEM) imaging techniques.

163 ethods such as scanning electron microscope (SEM), Fourier transform infrared spectrum (FT-IR), cycli

164 Scanning electron microscope (SEM), transmission electron microscope (TEM), x-ray diff

165 ethods such as scanning electron microscope (SEM), transmission electron microscope (TEM), x-ray diff

166 amined using a scanning electron microscope (SEM).

167 he Pd L-edge, Scanning electron microscopey (SEM) and Raman spectra, and direct magnetoelectric tenso

168 (XRF imaging and Fe EXAFS) and microscopic (SEM and confocal) techniques.

169 Scanning electron microscopy (SEM) analysis identified that exochorionic eggshell stru

170 Scanning Electron Microscopy (SEM) analysis of the biomass before and after the cell d

171 s shown in our Scanning Electron Microscopy (SEM) analysis.

172 ce changes via scanning electron microscopy (SEM) and atomic force microscopy (AFM), and Ti dissoluti

173 ombined use of scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM) confi

174 roscopy (AFM), scanning electron microscopy (SEM) and electrochemical techniques to confirm successfu

175 rthermore, the scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDXA) reveale

176 RD), Rheology, Scanning electron microscopy (SEM) and Fourier transform infra-spectroscopy (ATR-FTIR)

177 iable pressure scanning electron microscopy (SEM) and high vacuum SEM.

178 Scanning electron microscopy (SEM) and micro-computed tomography (micro-CT) showed the

179 oscopy (FTIR), scanning electron microscopy (SEM) and, energy-dispersive X-ray spectroscopy (EDX) ana

180 oscopy (FTIR), scanning electron microscopy (SEM) as well as alamar blue, acridine orange, and alizar

181 sualization by scanning electron microscopy (SEM) before performing NFRHT measurements.

182 Ex situ scanning electron microscopy (SEM) combined with energy-dispersive X-ray spectroscopy

183 py (FTIR), and scanning electron microscopy (SEM) equipped with energy dispersive X-ray analysis (EDX

184 Scanning electron microscopy (SEM) here also shows evidence of CPA in tunicate chordat

185 The Scanning electron microscopy (SEM) images demonstrated a relatively smooth surface wit

186 Acid-etched scanning electron microscopy (SEM) images of AIS demonstrated abnormal osteocytes that

187 Scanning electron microscopy (SEM) images of root sections were obtained for evaluatio

188 The scanning electron microscopy (SEM) images of the derived surfaces showed almost a unif

189 Scanning electron microscopy (SEM) images showed that mycelium modification covered wo

190 enhancement in scanning electron microscopy (SEM) images using a generative adversarial network.

191 by (13)C NMR, scanning electron microscopy (SEM) imaging, and fiber length distribution analysis, sh

192 M) and a novel scanning electron microscopy (SEM) method.

193 Finally, Scanning Electron Microscopy (SEM) permitted the morphological observation of IVDV-tre

194 In agreement, scanning electron microscopy (SEM) revealed abnormal fiber cell morphology in Tdrd7-/-

195 Scanning electron microscopy (SEM) revealed differences in epicuticular wax morphology

196 Scanning Electron Microscopy (SEM) revealed more compact and less porous matrices in t

197 combination of scanning electron microscopy (SEM) techniques.

198 rst time using scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) spectroscopy, th

199 raction (XRD), Scanning Electron Microscopy (SEM) with Energy Dispersive X-Ray Analysis (EDX) and Fou

200 nical testing, scanning electron microscopy (SEM), and biophysical modeling based on classic Hertz th

201 raction (XRD), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC).

202 py (ATR-FTIR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX).

203 scopy (FT-IR), Scanning Electron Microscopy (SEM), and X-ray Diffraction (XRD).

204 ed tomography, scanning electron microscopy (SEM), and X-ray diffraction (XRD).

205 c Voltammetry, Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM) and Raman Spectrosco

206 oscopy (FTIR), scanning electron microscopy (SEM), atomic force microscopy (AFM), differential pulse

207 erized through scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) surface area measurem

208 g time, color, scanning electron microscopy (SEM), damaged grains, amylose, protein content and extra

209 oscopy (FTIR), Scanning Electron Microscopy (SEM), Dynamic Light Scattering (DLS), Nuclear Magnetic R

210 raction (XRD), scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS) and c

211 action (pXRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy, and UV

212 nt microscopy, scanning electron microscopy (SEM), Fourier-Transform Infrared spectroscopy (FTIR), an

213 uster ion beam scanning electron microscopy (SEM), in which wide-area ion milling is performed on a s

214 assembled with scanning electron microscopy (SEM), is the most popular tool used in nanotechnology an

215 potential, and Scanning Electron Microscopy (SEM), respectively.

216 spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), scratch te

217 aracterized by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray Phot

218 oscopy (SNMS), Scanning electron microscopy (SEM), UV-Vis spectroscopy and Photo-electro-chemical (PE

219 roscopy (AFM), scanning electron microscopy (SEM), UV-Vis spectroscopy, X-ray diffraction (XRD) analy

220 oscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD) and differential scanning

221 Based on scanning electron microscopy (SEM), X-ray diffraction (XRD), energy-dispersive X-ray s

222 l results from scanning electron microscopy (SEM), X-ray diffraction (XRD), scanning transmission ele

223 copy (TEM) and scanning electron microscopy (SEM).

224 metry (CV) and scanning electron microscopy (SEM).

225 (cryo-ET), and scanning electron microscopy (SEM).

226 entified using scanning-electron microscopy (SEM).

227 in advance by scanning electron microscopy (SEM).

228 analyzed with scanning electron microscopy (SEM).

229 tion (XRD) and scanning electron microscopy (SEM).

230 nvestigated by Scanning Electron Microscopy (SEM).

231 cterized using scanning electron microscopy (SEM).

232 r analyzer and scanning electron microscopy (SEM).

233 bjecting it to Scanning Electron Microscopy (SEM).

234 observed from scanning electron microscopy (SEM).

235 crotome (ATUM) Scanning Electron Microscopy (SEM).

236 ture, using 3D scanning electron microscopy (SEM).

237 voltammetry, scanning electronic microscopy (SEM) and electrochemical impedance spectroscopy (EIS).

238 rescence and scanning electronic microscopy (SEM) was utilized to understand cell morphology.

239 g mass spectrometry (MALDI-TOF), microscopy (SEM, Raman), and microbiological techniques (CFU, OD(600

240 ments such as scanning electron microscopy, (SEM), transmission electron microscopy (TEM), X-ray diff

241 .0 +/- 0.30 to -30.8 +/- 0.19, milliUrey +/- SEM, P > 0.05).

242 -23.2 +/- 0.2 to -22.8 +/- 0.2 milliUrey +/- SEM.

243 del GRNs with the structural equation model (SEM) that can integrate gene expression and genetic pert

244 sed a demographic structural equation model (SEM) to demonstrate that a single axis of environmental

245 andom forests and Structural Equation Model (SEM).

246 We applied structural equation modeling (SEM) - GWAS aiming to explore interrelated dependency re

247 heory, we used structural equation modeling (SEM) to represent a general hypothesis for how 16 variab

248 etry (VBM) and structural equation modeling (SEM), latent hierarchical regression analyses were perfo

249 Structural equation models (SEMs) demonstrated a psychometric isomorphism between g

250 SEM into existing single-beam and multibeam SEM workflows should be straightforward, increasing reli

251 rmophilus, has been investigated by means of SEM, AFM and impedimetric measurements.

252 ich were further confirmed by the results of SEM analysis.

253 Based on SEM images and Fourier-transform infrared spectrums, the

254 ronmental drivers are common, suggesting our SEM-FLM approach is a widely applicable tool for explori

255 hen performed with BET, FTIR, XRD, TGA, PZC, SEM, and TEM analyses.

256 the accurately co-registered high-resolution SEM images of the same samples.

257 By using this technique, higher resolution SEM images can be taken faster, while also reducing both

258 frequency spectra matching higher resolution SEM images of the same fields-of-view.

259 erring unresolved features in low-resolution SEM images and comparing them with the accurately co-reg

260 Block Face Scanning Electron Microscopy (SBF-SEM) and transmission electron microscopy enabled ultras

261 Cross sectional SEM images of the broken fiber showed that the thickness

262 ission scanning electron microscope (FE-SEM, SEM-Mapping), scanning transmission electron microscopy

263 OZ), 1-aminohydantoine (AHD), semicarbazide (SEM) and 3,5-dinitrosalicylic acid hydrazide (DNSH).

264 Semillon (SEM) and Sauvignon Blanc (SAB) juices (20L in triplicate

265 and develop an algorithm named fused sparse SEM (FSSEM), to jointly infer GRNs under two conditions,

266 croscopy and energy-dispersive spectrometry (SEM-EDS), suggesting anthropogenic sources.

267 e characterized through UV-VIS spectrometry, SEM, optical microscopy, and light exposure.

268 M with energy dispersive X-ray spectroscopy (SEM-EDS).

269 d with energy-dispersive X-ray spectroscopy (SEM-EDS).

270 copy - energy-dispersive X-ray spectroscopy (SEM-EDX) were selected.

271 y plus energy-dispersive X-ray spectroscopy (SEM/EDS), and Fourier transform infrared (FTIR) micro-sp

272 d with energy dispersive X-ray spectroscopy (SEM/EDX) method that enabled detection and semiquantific

273 oscopy/energy-dispersive X-ray spectroscopy (SEM/EDX), and electrochemical impedance spectroscopy (EI

274 ensor were confirmed by UV-vis spectroscopy, SEM, TEM and XRD analysis.

275 analysis using a serial section array (SSA)-SEM identified virus particles in vesicles within the cy

276 Computer-assisted processing of SSA-SEM images from each cell type enabled three-dimensional

277 In summary, SEM-GWAS offered new insights on the relationships among

278 TEM, SEM-EDX, FT-IR, VSM techniques were applied for characte

279 erials were thoroughly characterized by TEM, SEM, XPS, FTIR, and nitrogen-adsorption surface area ana

280 ogical characteristics were assessed by TEM, SEM-EDX, X-ray photoelectron spectroscopy and vibrating

281 SMC-derived intermediate cells, termed "SEM" cells (stem cell, endothelial cell, monocyte), were

282 The SEM analysis revealed a change in the morphology from fi

283 The SEM images demonstrated that starch without alkali exhib

284 The SEM micrographs confirmed the successful capturing of E.

285 The SEM-EDX analysis has shown the maximum quantity of carbo

286 This illustrates how these SEM images, publicly available to the research community

287 sion (alpha-TCsNe) was characterized through SEM, FTIR and XRD techniques.

288 hesized CS-PAEO-Nm was characterized through SEM, FTIR, and XRD and evaluated for improved biological

289 The TPEs were characterized through SEM, optical profilometry and cyclic voltammetry.

290 ling was identified as a regulator of SMC to SEM cell transition, and RA signaling was dysregulated i

291 elocytic leukemia, blocked SMC transition to SEM cells, reduced atherosclerotic burden, and promoted

292 0 post PPA treatment to (Mean: 193.47 um +/- SEM: 6.673 um) versus (154.16 um +/- 9.95 um) in control

293 Again, using SEM, we evaluated the ability of this "stressor network"

294 rom the ZrC(1-x) structure is analysed using SEM and Raman spectroscopy.

295 d reaction products were characterized using SEM-EDS and synchrotron muXRD and muXRF.

296 ng electron microscopy (SEM) and high vacuum SEM.

297 Ninhydrin assay, FTIR, WAXD, SEM and mechanical tests documented successful crosslink

298 the fabrication steps were carried out with SEM and AFM monitoring.

299 thesized and characterized using FT-IR, XRD, SEM and VSM techniques.

300 bionanocomposites were evaluated using, XRD, SEM, TEM, FT-IR and final contact angle.