ライフサイエンスコーパス: SEM

1 SEM and EDX analyses confirmed the presence of calcific

2 SEM and FT-IR analysis were studied to characterize the

3 SEM and TEM analysis showed that TRIP-1 promoted the nuc

4 SEM and TEM characterization results indicated that grap

5 SEM images of the modified surface show high order and h

6 SEM images show distinct shedding of microvilli-like fea

7 SEM images showed that extracted polysaccharides had a r

8 SEM images showed that PAA/QU/beta-CD-IC-NF were bead-fr

9 SEM imaging detailed the membrane-fusion process in four

10 SEM imaging revealed ED deposition distributed MnO2 thro

11 SEM reveals persistent damage to some surviving outer ha

12 SEM studies show that irradiated Ta surfaces undergo sig

13 SEM studies suggested the morphological intactness of th

14 SEM, FTIR and mechanical tests were further employed to

15 SEM-EDS analysis shows that the fossils are composed of

16 SEM-EDX analysis showed that As was localized largely on

17 Roughly 20,000 SEM images were manually classified into 10 categories t

18 = 0.36, P = 0.001), and ALMBMI (beta = 0.04, SEM = 0.02, P = 0.013) in men and with LLM in women (bet

19 , rLTL was associated with ALM (beta = 1.11, SEM = 0.46, P = 0.017), LLM (beta = 1.20, SEM = 0.36, P

20 n supragranular layers (mean cells/mm(2) +/- SEM, Sham = 16 +/- 0.971, TBI = 25 +/- 1.51, P = 0.001).

21 1, SEM = 0.46, P = 0.017), LLM (beta = 1.20, SEM = 0.36, P = 0.001), and ALMBMI (beta = 0.04, SEM = 0

22 treated monthly increased at a rate of 1.22, SEM 0.34 points per year compared with 2.92, SEM 0.27 po

23 ping and overlap of fibrils than standard 2D SEM images, likely due to artifacts in SEM introduced by

24 plus 8 mg/day) was associated with a 24.4% (SEM 7.7%) decrease from baseline in mean UPCR (change in

25 b and placebo (least-squares mean rank 56.6 [SEM 4.5] vs 68.3 [4.5]; rank-based treatment difference

26 % vs 19.6%; P = 0.04) and count (mean: 12.7, SEM: +/- 5.9 vs 1.9; +/- 1.2; P = 0.01) were significant

27 ) in men and with LLM in women (beta = 0.78, SEM = 0.35, P = 0.026).

28 SEM 0.34 points per year compared with 2.92, SEM 0.27 points per year (p=0.0002) for the 21 patient c

29 ic (UV-vis, FTIR, XPS) and microscopic (AFM, SEM, and TEM) techniques.

30 ndothelial cytoskeletal structure using AFM, SEM, and immunofluorescence.

31 scopy with energy dispersive X-ray analysis (SEM/EDX), scanning transmission X-ray microscopy (STXM)

32 ysis of their metabolites AHD, AOZ, AMOZ and SEM, respectively while nitroimidazole residues; ronidaz

33 The postoperative appearance and SEM features warrant further assessment of the PPC integ

34 Using cryoTEM and SEM, the early reaction stages taking place during arago

35 ere also processed and submitted to FTIR and SEM analysis to evaluate the remineralization induced by

36 n of the thin film was conducted by FTIR and SEM.

37 and document it with drawings and light and SEM micrographs.

38 The use of optical microscopy and SEM revealed that needle-shaped crystals grow as cluster

39 was also assessed by confocal microscopy and SEM.

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

41 g UV-Vis, TGA, FT-IR, Raman Spectroscopy and SEM techniques.

42 Visual and SEM observations confirmed the flocculation action of th

43 XRD, contact angle, SEM, AFM and SECM studies revealed that the surface of t

44 -infected subjects (mean duration of ART [+/-SEM], 11 +/- 1 years), but not among non-HIV-infected su

45 g II receptor and resulted in an average (+/-SEM) of 3.7+/-2.2, 72.3+/-18.6 (P<0.001), and 239.4+/-34

46 Multi-beam SEM and our presented methodology enable an unprecedente

47 using high-resolution cryo-focused ion beam-SEM serial imaging.

48 The obtained microparticles were analysed by SEM, XRD and DSC.

49 d thorn-like ZnO-NPs (morphology assessed by SEM) were well accounted to be less than 50 nm with the

50 nism with ITO electrode are characterized by SEM, EDX and XRD analyses.

51 studied, and catalysts are characterized by SEM, EDX, and XRD techniques.

52 cal structure of CPCMs were characterized by SEM, FT-IR and XRD.

53 nd Bombyx mori samples were characterized by SEM-EDX, FT-IR, XRD and TGA-DSC techniques.

54 the enzymatic pretreatment was confirmed by SEM and FTIR.

55 raphy and surface chemistry as determined by SEM microscopy and RAMAN spectroscopy.

56 itted to our laboratory and were examined by SEM and EDX in order to identify the morphologic feature

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

58 Sorbent characterization was investigated by SEM, FT-IR, EDX and VSM.

59 bioactive nanocomposite films as revealed by SEM and AFM images.

60 easing the number of surface pores; shown by SEM images and XRD data.

61 nce, and polyphenol, microstructure changes (SEM).

62 l deformation, as shown in the false-colored SEM image.

63 Optical reflectivity complements SEM and demonstrates a vertical growth of surface struct

64 mperature scanning electron microscopy (cryo-SEM) was adopted to image the fully hydrated gelatin net

65 mperature scanning electron microscopy (cryo-SEM).

66 l models increased the area under the curve (SEM) for predicting the renal outcome from 0.68 (0.02) t

67 ectrode has been monitored by time dependent SEM study.

68 Detailed SEM-EDX analyses showed reaction zones similar to those

69 Fluorescence microscopy and FE-SEM indicated simultaneous improvement in antiadhesive a

70 -vis, FT-IR, and Raman spectroscopies and FE-SEM, which indicated attachment of NR on po-Gr sheets.

71 of the modified electrodes was studied by FE-SEM and AFM.

72 -NSs were characterized systematically by FE-SEM, EDS, UV/Vis., FTIR spectroscopy, powder XRD, and XP

73 The morphological analysis by FE-SEM, on solid samples, showed arrangement of fibers into

74 ld emission scanning electron microscope (FE-SEM) imaging and energy dispersive spectroscopy (EDS) we

75 ld emission scanning electron microscopy (FE-SEM) and X-ray photoelectron spectroscopy (XPS) characte

76 ld emission-scanning electron microscopy (FE-SEM), Fourier-transform infrared spectroscopy (FTIR), hi

77 FIB-SEM 3D reconstructions showed considerably less lateral

78 mage acquisition while greatly improving FIB-SEM reliability, allowing the system to operate for mont

79 d ion beam scanning electron microscopy (FIB-SEM) and serial sectioning transmission electron microsc

80 d Ion Beam Scanning Electron Microscopy (FIB-SEM) can automatically generate 3D images with superior

81 d ion beam scanning electron microscopy (FIB-SEM), can be used to generate 3D image datasets for visu

82 ratures, and used X-ray microtomography, FIB-SEM nanotomography and neutron diffraction to reveal the

83 This study demonstrates the utility of FIB-SEM for 3D imaging of collagen gels and quantitative ana

84 Obstacles blocking wider adoption of FIB-SEM include slow imaging speed and lack of long-term sys

85 and embedded the samples, and performed FIB-SEM imaging.

86 s assessed by comparing fiber diameters from SEM and CLSM to be between 0.46% to 3.8% of the SEM refe

87 complementary elemental quantification from SEM/EDX.

88 These findings along with results from SEM, TEM, and XRPD studies support our hypothesis that w

89 il-1,3,5-triazine and characterized by FTIR, SEM and elemental analysis and used adsorbent for column

90 d podocyte loss (podocytes per glomerulus +/-SEM at 8 weeks: 667+/-40, n=4; at 20 weeks: 364+/-18 wit

91 rd 2D SEM images, likely due to artifacts in SEM introduced by dehydration.

92 fraction of coherently aligned nanowires in SEM images.

93 material by microscopy techniques including SEM, TEM and confocal microscopy is presented.

94 nanobiocatalyst was characterized by FT-IR, SEM and XRD.

95 en synthesized and characterized with FT-IR, SEM, EDX, TEM, UV-Visible, XRD and TG/DTA techniques.

96 e results from single-equation-estimation IV-SEM were notably different, revealing the impact of weak

97 ariables simultaneous equations modeling (IV-SEM) to examine physical activity relative to body mass

98 round such spiking expectation maximization (SEM) networks whose combined outputs are mediated by ITD

99 nosis in 32 of 63 infants (50.8%) at a mean (SEM) of 33.1 (5.6) days of life with a mean (SEM) turnar

100 SEM) of 33.1 (5.6) days of life with a mean (SEM) turnaround time of 13.0 (0.4) days.

101 The mean (SEM) age for infants participating in the study was 28.5

102 udy was 28.5 (1.7) days; of these, the mean (SEM) age was 29.0 (2.2) days for infants undergoing prob

103 ints below the normative mean, and the mean (SEM) total change in the MCCB during receipt of placebo

104 Mean +/- SEM pre- and postfilter venous plasma citrate concentrat

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

106 treatments (P < 0.001) [Bar15/0LS (mean +/- SEM), 169 +/- 14; Control2, 164 +/- 20; Bar15/0, 144 +/-

107 n extraction (TBI = 73.13 +/- 5.23% mean +/- SEM, Sham = 92.29 +/- 5.56%, P < 0.01), motor cortex sho

108 s index (in kg/m(2)): 25.9 +/- 0.4 (mean +/- SEM)] participated in a parallel-group randomized trial

109 s included 5 men and 5 women with a mean +/- SEM age of 61 +/- 4 y (range: 42-84 y) and body mass ind

110 Sixteen women with a mean +/- SEM body mass index (in kg/m(2)) of 44.1 +/- 1.6 were in

111 After the CR intervention, a mean +/- SEM weight loss of 9.0 +/- 0.6 kg was observed in the CR

112 x (in kg/m(2)): 31 +/- 0.5] adults (mean +/- SEM age: 28 +/- 2 y; 17 men and 13 women) consumed a con

113 Data are presented as mean +/- SEM.

114 sion.Eight male endurance athletes (mean +/- SEM age: 29 +/- 2 y; peak oxygen consumption: 66.8 +/- 1

115 pernatant after hyperoxia exposure (mean +/- SEM, 1,879 +/- 278 vs. 842 +/- 119 resorufin arbitrary f

116 in milk collected in rural Gambia (mean +/- SEM: 473 +/- 55 compared with 103 +/- 16 nmol/mL, respec

117 ein or leucine ingestion, the grand mean +/- SEM plasma 3-HIB concentration decreased (from 35 +/- 2

118 roxide after exposure to hyperoxia (mean +/- SEM, 89,807 +/- 16,616 vs. 162,706 +/- 25,321 MitoSOX Re

119 to-duodenum [-22%, -988 +/- 379 kJ (mean +/- SEM), Tukey's post hoc, P < 0.05]; and increased glucago

120 ecific activity resulted in a lower mean +/- SEM tumor load by histopathology (vital tissue, 4 +/- 2

121 .Eight older women and 8 older men [mean +/- SEM age: 72 +/- 1 y; body mass index (in kg/m(2)): 25 +/

122 in 14 healthy volunteers [50% men; mean +/- SEM age: 25 +/- 2 y; mean +/- SEM body mass index (BMI;

123 entage of body fat gain over 12 mo (mean +/- SEM: dairy 0.40% +/- 0.53% > control; P < 0.45).

124 Healthy, overweight or obese [mean +/- SEM body mass index (in kg/m(2)): 31 +/- 0.5] adults (me

125 iod of 3 h, with peak reductions of mean +/- SEM 7 +/- 3 mm Hg 2 h after MC consumption relative to t

126 s greater in recuperated offspring (mean +/- SEM: 12 +/- 2 mum) than in controls (5 +/- 0.5 mum) (P <

127 es with CFS were 53 (+/-2.8) y old (mean +/- SEM; range, 21-67 y).

128 d clinical trial, 173 participants (mean +/- SEM: age 27 +/- 1 y) who self-identified as having seaso

129 stration compared with the placebo (mean +/- SEM: 720 +/- 58 compared with 796 +/- 45 kcal; P = 0.08)

130 er maximal oxygen consumption rate (mean +/- SEM, 107 +/- 8 vs. 235 +/- 22 pmol/min/30,000 cells; P <

131 ypercapnia is higher in young SHRs (mean +/- SEM: 179 +/- 11% increase) than in age-matched normotens

132 d reactive ones [LN transformation (mean +/- SEM) healthy: 3.9 +/- 0.02 muM/mM; completely tolerant:

133 lted in significant declines of Vt (mean +/- SEM, 9.3 +/- 0.6 to 5.6 +/- 0.2 ml/kg; P < 0.0001), tran

134 lel-design study, 41 men and women [mean +/- SEM age: 35 +/- 2 y; body mass index (in kg/m(2)): 31.5

135 men; mean +/- SEM age: 25 +/- 2 y; mean +/- SEM body mass index (BMI; in kg/m(2)): 23 +/- 1].

136 The low-frequency component (mean [SEM], 52.7 [4.0] nu vs 39.9 [3.8] nu; P = .03) and the l

137 Of the controls (mean [SEM] age, 33.7 [8.8] years), 10 (42%) were male and 14 (

138 15), organ transplant-associated cSCC (mean [SEM] expression, 3.01 [0.54]; P = .005), and infiltrativ

139 06 [1.27]; P = .05), superficial cSCC (mean [SEM] expression, 3.58 [1.50]; P = .15), organ transplant

140 t necessary to obtain the higher dose (mean [SEM], 61% [0.02%] vs 39% [0.02%]; Cohen d = 0.40; P < .0

141 24.0 [145.5]; P = .01), lingual gyrus (mean [SEM], 11 996.0 [531.5] vs 13 838.1 [441.9]; P = .05), an

142 gnificantly reduced total hippocampal (mean [SEM], 8309.6 [175.0] vs 9024.0 [145.5]; P = .01), lingua

143 ared with nonuser control individuals (mean [SEM], 3801.0 [415.7] U vs 2413.3 [325.0] U; P = .01) con

144 ands in cSCC with perineural invasion (mean [SEM] expression, 5.06 [1.27]; P = .05), superficial cSCC

145 red with nonuser control participants (mean [SEM], 46.5 [3.7] nu vs 57.8 [3.6] nu; P = .04).

146 low frequency to high frequency ratio (mean [SEM], 1.37 [0.19] vs 0.85 [0.18]; P = .05) were signific

147 = .05), and superior temporal sulcus (mean [SEM], 4697.8 [192.0] vs 5446.0 [159.6]; P = .05) gray ma

148 Mean+/-SEM maximal change in Hb from baseline (DeltaHb(max)), t

149 Coronary flow reserve was 2.8+/-0.2 (mean+/-SEM) in control and 1.8+/-0.1 in AS (P<0.005) and was no

150 Peak Vo2 was reduced by 34+/-2% (mean+/-SEM, P<0.001) in HFpEF compared with controls of similar

151 2 patients with IgA nephropathy for a mean+/-SEM period of 14+/-10.2 years, during which clinical and

152 ytes and endothelial cells after AKI (mean+/-SEM: 3.3+/-0.1 microm before injury versus 12.5+/-0.2 mi

153 ) and increased cross-sectional area (mean+/-SEM: 21.9+/-0.4 microm(2) in control versus 24.1+/-0.6 m

154 Patients had mean+/-SEM ultrafiltration rates of 3.8+/-2.9 ml/kg per hour du

155 ents with HRM than those without HRM (mean+/-SEM: 1.95+/-0.43 versus 1.67+/-0.32 for LMCA with versus

156 apillary number at later time points (mean+/-SEM capillaries/high-power field: 67.6+/-4.7 in control

157 The mean+/-SEM differences in the change over 6 months between stud

158 samples from coastal Georgia, USA (means +/- SEM: 382 +/- 35 versus 73 +/- 24 nmol L(-1) d(-1) , Mann

159 88 +/- 3 kg; body fat: 16% +/- 1% (means +/- SEMs)] received primed continuous l-[ring-(2)H5]phenylal

160 CEHC (all values are least-squares means +/- SEMs: 0.6 +/- 0.1 compared with 1.0 +/- 0.1 mumol/g crea

161 /ml [means +/- standard errors of the means {SEM}; P = 0.0001).

162 Using the scanning electron microscope (SEM) and micro computed tomography (micro-CT), it was ob

163 Installed in a scanning electron microscope (SEM) field emission gun, our tip shows a current density

164 ion beam (FIB) scanning electron microscope (SEM) imaging and scanning transmission electron microsco

165 signal in the scanning electron microscope (SEM) is a technique gaining impulse for its ability to e

166 ccomplished by scanning electron microscope (SEM), electrochemical impedance spectroscopy (EIS) and c

167 ope (AFM) or a scanning electron microscope (SEM), optical tweezers, and focused electron-beam nanoma

168 roscopy (XPS), scanning electron microscope (SEM), quartz crystal microbalance (QCM), contact angle (

169 es obtained by scanning electron microscope (SEM).

170 y (EDX) with a scanning electron microscope (SEM).

171 re analyzed via scanning electron microscope(SEM) and energy dispersive spectrometry(EDS).

172 chieved using scanning electron microscopic (SEM) and Energy Dispersive X-Ray Analysis (EDX) techniqu

173 A scanning electron microscopic (SEM) image of the Au NBs revealed a NB-shaped Au structu

174 anning and transmission electron microscopy (SEM and TEM), Fourier transformed infrared (FT-IR) spect

175 chemistry and scanning electron microscopy (SEM) analysis, a Fourier-transform infrared microspectro

176 Scanning electron microscopy (SEM) and AFM imaging of C. albicans confirmed the polymo

177 try (FTIR) and scanning electron microscopy (SEM) and applied as a sorbent for selective magnetic sol

178 so revealed by scanning electron microscopy (SEM) and atomic force microscopy (AFM) analysis, respect

179 yses of GMs by scanning electron microscopy (SEM) and atomic force microscopy (AFM) feature a uniform

180 gree well with scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS) an

181 aracterized by scanning electron microscopy (SEM) and energy dispersive X-ray (EDX).

182 action (pXRD), scanning electron microscopy (SEM) and Fe 2p X-ray photoelectron spectroscopy (XPS).

183 spectroscopy, scanning electron microscopy (SEM) and gas chromatography-flame ionization detection (

184 observed with Scanning Electron Microscopy (SEM) and identified using Energy Dispersive X-ray (EDX)

185 Here we use scanning electron microscopy (SEM) and multiplex coherent anti-Stokes Raman scattering

186 aracterized by scanning electron microscopy (SEM) and profilometry.

187 raction (XRD), scanning electron microscopy (SEM) and Raman spectroscopy.

188 s confirmed by Scanning Electron Microscopy (SEM) and Raman Spectroscopy.

189 be observed by scanning electron microscopy (SEM) and Raman spectroscopy.

190 termined using scanning electron microscopy (SEM) and scanning electron microscopy with energy disper

191 spectroscopy, scanning electron microscopy (SEM) and scanning transmission electron microscopy (STEM

192 raction (XRD), scanning electron microscopy (SEM) and transmission electron microscope (TEM) techniqu

193 Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images r

194 aracterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM).

195 re observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM).

196 rizations with scanning electron microscopy (SEM) and transmission electron microscopy (TEM).

197 roscopy (AFM), scanning electron microscopy (SEM) and X-ray diffraction (XRD).

198 copy (AFM) and scanning electron microscopy (SEM) confirmed the size, spherical nature and smooth sur

199 tammetry (CV), Scanning Electron Microscopy (SEM) Electrochemical Impedence Spectroscopy (EIS), enlig

200 Scanning Electron Microscopy (SEM) has been used to demonstrate selective immobilizati

201 d conventional scanning electron microscopy (SEM) have been routinely used to identify and classify v

202 ion (SXRD) and scanning electron microscopy (SEM) have been used to measure and correlate enamel crys

203 Scanning electron microscopy (SEM) images provide insight into the morphology of the j

204 multi-view 2D scanning electron microscopy (SEM) images.

205 s evident from scanning electron microscopy (SEM) imaging of their xerogels, XGh (xerogel made from h

206 t labeling and scanning electron microscopy (SEM) imaging show that direct fusion of MkMPs into HSPCs

207 Scanning electron microscopy (SEM) imaging showed a non-porous and finely meshed micro

208 examined using scanning electron microscopy (SEM) showed characteristics of melting and blistering of

209 Scanning electron microscopy (SEM) was used for surface characterization.

210 opy (FTIR) and scanning electron microscopy (SEM) were also used to evaluate the remineralization ind

211 mical methods, scanning electron microscopy (SEM), and atomic force microscopy (AFM).

212 roscopy (EIS), scanning electron microscopy (SEM), and electron dispersion X-ray spectrometry (SEM/ED

213 raction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS) wer

214 roscopy (XPS), scanning electron microscopy (SEM), and in situ X-ray diffraction (XRD).

215 roscopy (TEM), scanning electron microscopy (SEM), and powder X-ray diffraction (PXRD).

216 emonstrated by scanning electron microscopy (SEM), and providing protection against protein oxidation

217 spectroscopy, scanning electron microscopy (SEM), and spectrofluorimetry to characterize the materia

218 nvestigated by scanning electron microscopy (SEM), and the formation of beta-phase was confirmed by X

219 mography (CT), scanning electron microscopy (SEM), and transition electron microscopy (TEM).

220 contact angle, scanning electron microscopy (SEM), atomic force microscopy (AFM) and scanning electro

221 ellipsometry, scanning electron microscopy (SEM), atomic force microscopy (AFM), and synchrotron rad

222 roscopy (TEM), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (

223 Scanning electron microscopy (SEM), electron microprobe analysis (EMPA), and micro-X-r

224 terized by the scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and

225 as assessed by scanning electron microscopy (SEM), immunofluorescence microscopy, histochemistry and

226 field emission scanning electron microscopy (SEM), Raman spectra, Fourier Transform infrared spectros

227 was studied by scanning electron microscopy (SEM), Raman spectroscopy, contact angle and zeta potenti

228 are studied by scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM) a

229 oscopy (FTIR), scanning electron microscopy (SEM), SEM-energy dispersive X-ray (EDX) mapping and atom

230 raction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray p

231 raction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray

232 raction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), photo elec

233 acterised with scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spec

234 ized using the scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diff

235 ried out using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diff

236 ut by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diff

237 Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray phot

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

239 igh-resolution scanning electron microscopy (SEM), wavelength-dispersive electron probe microanalysis

240 as analyzed by Scanning Electron Microscopy (SEM), X-ray-tomography and Fourier-Transform Infrared sp

241 observed from scanning electron microscopy (SEM).

242 opy (AFM), and scanning electron microscopy (SEM).

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

244 (Py-GC/MS) and scanning electron microscopy (SEM).

245 s estimated by scanning electron microscopy (SEM).

246 opy (CLSM) and scanning electron microscopy (SEM).

247 try (LSSV) and scanning electron microscopy (SEM).

248 on (p-XRD) and scanning electron microscopy (SEM).

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

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

251 collected for scanning electron microscopy (SEM).

252 ructed using scanning electronic microscopy (SEM) images taken from different view directions.

253 l techniques (e.g., fluorescence microscopy, SEM, AFM), and show that the PFBs continue to be mobile

254 ith those from structural equation modeling (SEM), which specifically accounted for shared familial e

255 ize) and used structural equation modelling (SEM) to achieve a system-level understanding of how arid

256 Using structural equation models (SEMs), we assessed the impact of vascular health on AD b

257 Using this new SEM, we acquired very low-noise, high-resolution images

258 The results of (13)C NMR, SEM, DSC and X-ray analyses showed that these MC levels

259 y around 90% of a test dataset consisting of SEM images, while reduced accuracy was found in the case

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

261 The results of our SEM were supported by results showing that rates of hopb

262 These investigations are coupled to parallel SEM studies that image crystalline sodium superoxide (Na

263 omposite and ball with optical profilometry, SEM, XPS and Auger spectroscopy.

264 closed core CNFs, as characterized by Raman, SEM and TEM.

265 Mean tumor-to-kidney ratios +/- SEM were 19 +/- 5, 10 +/- 5, and 2 +/- 0 for high, inter

266 RR was visualized by AFM and high-resolution SEM, which also showed approximately 5 nm sized Pt parti

267 (TEM) and serial block face scanning EM (SBF-SEM) with 3D reconstruction.

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

269 (FTIR), scanning electron microscopy (SEM), SEM-energy dispersive X-ray (EDX) mapping and atomic for

270 and electron dispersion X-ray spectrometry (SEM/EDX).

271 y with energy dispersive X-ray spectroscopy (SEM-EDX).

272 ty, solubility, moisture content, structure (SEM, XRD), FT-IR and sensory properties.

273 ron microscopy and energy dispersive system (SEM/EDS) analysis.

274 hesized materials were characterized by TEM, SEM, UV-Vis, XRD, XPS, EIS, fluorescence, and photoelect

275 were fabricated and characterized with TEM, SEM and XRD.

276 te of the art techniques including XRD, TEM, SEM and XPS.

277 The SEM and XRD results testified a slightly increase of the

278 particle shape and size as indicated by the SEM images.

279 composite was carefully characterized by the SEM, TEM, FT-IR, XRD and so on.

280 o classify and label images generated by the SEM.

281 However, the SEM of the treatment effect increased (decreased precisi

282 contrast studies by energy-filtering in the SEM from silicon p-n junction specimens that were etched

283 tabilities, accounting for almost all of the SEM heritability for hypertension.

284 and CLSM to be between 0.46% to 3.8% of the SEM reference values.

285 ross diseases and an average of 57.3% of the SEM-estimated heritabilities, accounting for almost all

286 The training set was used to retrain on the SEM dataset and to compare many convolutional neural net

287 The SEMs showed that (1) vascular health had a significant d

288 ir-excluded conditions for 6 months prior to SEM/EDS and muXANES analysis to determine V host phases

289 om Green River Shale and characterized using SEM, TGA, DSC, and nitrogen adsorption.

290 gomonas sp.-(f)Si NP was characterized using SEM.

291 We show here, using SEM and confocal microscopy, that platelet-poor-plasma f

292 rphology and gluten protein structure, using SEM, light and immunofluorescent microscopy.

293 s were collected in a novel manner utilizing SEM stubs.

294 These materials are characterized with SEM, XRD, TEM, SAED, EDX, XPS, UV-visible spectroscopy,

295 d by N2GA hysteresis loop is consistent with SEM observation on clay inter-crystalline pores while BJ

296 rs, were found than previously reported with SEM.

297 zed nanoparticles were characterized by XRD, SEM, TEM, FTIR, TGA, DSC and UV-visible spectroscopy.

298 th red phosphorus, and characterized by XRD, SEM, XPS, XRF, SAED and TEM measurements.

299 acterized by FTIR, magnetic hysteresis, XRD, SEM and N2-sorption measurements.

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