ライフサイエンスコーパス: scanning

1 by the Food and Drug Administration for MRI scanning).

2 CT was performed, and the use of multiphase scanning.

3 r liking of the presented person during fMRI scanning.

4 d healthy controls (n=68) also underwent MRI scanning.

5 h resolution light sheet system without beam scanning.

6 vidual illusion magnitude and structural MRI scanning.

7 g the polarization angle of the laser during scanning.

8 associations with mood state at the time of scanning.

9 ts and underwent comparative (68)Ga-THP-PSMA scanning.

10 o types of memory test while undergoing fMRI scanning.

11 s because 3 patients withdrew consent before scanning.

12 d were appropriately reprogrammed before the scanning.

13 prospective multicenter study of FDG-PET/CT scanning 12 weeks after CCRT in newly diagnosed patients

14 ntified the same particles as those found by scanning a filter area with IR-microscopy.

15 GFET) on silicon carbide (SiC) substrates by scanning a focused laser beam across the GFET.

16 ustic sources were sequentially addressed by scanning a focussed optical beam across the proximal end

17 was performed by adrenal computed tomography scanning and adrenal vein sampling, using strict criteri

18 at influenced dose variation were multiphase scanning and institutional protocol choices.

19 he core and aryl appendages was performed by scanning and matrix libraries synthesized by the multipl

20 In 31 patients, bone scanning and radiologic imaging were performed for preth

21 imaging modalities, including, for example, scanning and spectroscopic techniques.

22 We used atomic force microscopy (AFM), scanning and transmission electron microscopy (SEM and T

23 Selected lesions were also examined by scanning and transmission electron microscopy and by sta

24 ching, dual-source, split-filter, sequential-scanning, and dual-layer detector systems.

25 Using a crystal scanning approach, we determine the high-resolution stru

26 Although spiral scanning avoids the sudden changes in the beam location

27 Using genetic lineage-tracing and scanning-block face electron microscopy, we show that in

28 Differential Scanning Calorimeter (DSC) showed better thermal stabili

29 Differential Scanning Calorimeter analysis showed that the transition

30 results are consistent with the differential scanning calorimetry (DSC) data for the peaks correspond

31 l crystallization studies using differential scanning calorimetry (DSC) showed increased inhibitory e

32 roperties of starch depicted by differential scanning calorimetry (DSC).

33 C were further characterized by Differential Scanning Calorimetry (DSC).

34 We used pressure perturbation differential scanning calorimetry (PPC) that studies a system on the

35 multaneous thermogravimetry and differential scanning calorimetry (TG-DSC), evolved gas analysis (TG-

36 Complete characterization from differential scanning calorimetry and (1)H NMR and UV-vis-NIR spectro

37 An anomaly in differential scanning calorimetry has been reported in a number of me

38 The differential scanning calorimetry studies demonstrated that the sampl

39 osphoethanolamine (POPE), using differential scanning calorimetry, and sequential (2)H and (31)P soli

40 ectroscopy, cyclic voltammetry, differential scanning calorimetry, single-crystal X-ray diffraction,

41 etic resonance spectroscopy and differential scanning calorimetry, together with dye leakage assays.

42 permeation chromatography, and differential scanning calorimetry.

43 onance and thermal behaviour by differential scanning calorimetry.

44 f the heat capacity measured by differential scanning calorimetry.

45 we show the usefulness of live-imaging laser scanning confocal microscopy to investigate coral health

46 r variability as well as to filter anomalous scanning data.

47 mpower researchers analyzing deep mutational scanning data.

48 al tensile stress perpendicular to the laser scanning direction is elevated due to a significant temp

49 we sought to demonstrate how deep mutational scanning (DMS) could provide details about important fun

50 %) patients with only 1 patient requiring re-scanning due to motion blur.

51 ve stability assessment for simultaneous PET scanning during functional MRI studies was performed wit

52 coated microelectrode used as the tip in the scanning electrochemical microscope (SECM).

53 ns in high resolution imaging with nanoscale scanning electrochemical microscopy (SECM) and neurochem

54 determined using cyclic voltammetry (CV) and scanning electrochemical microscopy (SECM) approach curv

55 Scanning electrochemical microscopy (SECM) can map surfa

56 iderably higher than previously reported for scanning electrochemical microscopy (SECM) imaging of mo

57 , in which Raman microscopy is combined with scanning electrochemical microscopy (SECM) in order to p

58 anning ion conductance microscopy (SICM) and scanning electrochemical microscopy (SECM) measurements

59 Here we report on the application of scanning electrochemical microscopy (SECM) to enable the

60 eration/substrate collection (TG/SC) mode of scanning electrochemical microscopy (SECM).

61 al activity in individual cancer cells using scanning electrochemical microscopy (SECM).

62 ode (25 mum diameter each) for use as a dual scanning electrochemical microscopy probe.

63 olved O2 by photosystem 2 using a positioned scanning electrochemical microscopy tip are evaluated.

64 means of electron impedance spectroscopy and scanning electrochemical microscopy.

65 of single aerographite tetrapods via in situ scanning electron and atomic force microscopy measuremen

66 electrochemical characterisation, as well as scanning electron and atomic force microscopy.

67 Scanning electron micrographs revealed that the sonicate

68 mography (CT), plasma focused ion beam (FIB) scanning electron microscope (SEM) imaging and scanning

69 nocomposites properties were accomplished by scanning electron microscope (SEM), electrochemical impe

70 uct nanomechanical experiments in an in situ scanning electron microscope and show that micrometer-si

71 tituents were mapped using elemental display scanning electron microscope images.

72 ackscatter diffraction (EBSD) technique in a scanning electron microscope to non-destructively charac

73 Focused ion beam/scanning electron microscope tomography reveals the key

74 d composition distribution were analyzed via scanning electron microscope(SEM) and energy dispersive

75 ing of the nanobiosensor e.g. field emission scanning electron microscope, cyclic voltammetry and ele

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

98 Scanning electron microscopy analysis confirmed the pres

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

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

101 Scanning electron microscopy and spectroscopic ellipsome

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

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

104 Confocal and scanning electron microscopy confirm removal of biofilm

105 Scanning electron microscopy documents ommatidial organi

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

107 Serial block face scanning electron microscopy of zebrafish cones revealed

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

109 Field emission scanning electron microscopy revealed that ethanol solut

110 METHODS AND Scanning electron microscopy revealed that the synthesis

111 Scanning electron microscopy sampling showed a generally

112 Scanning electron microscopy showed that NaOH steeping p

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

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

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

116 Furthermore, scanning electron microscopy was used to investigate thr

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

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

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

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

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

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

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

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

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

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

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

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

129 Disk surface morphology was evaluated by scanning electron microscopy.

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

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

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

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

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

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

136 morula and blastocyst-like stages by light, scanning electron or three-dimensional confocal scanning

137 es and wax micro-structures were examined by scanning emission microscopy, and hydrophobicities of pl

138 lting in increased interepithelial cell (EC) scanning, expression of antimicrobial genes, and glycoly

139 tails separated by <25 nm where conventional scanning failed to acquire sufficient signal.

140 technologies with faster scan speeds, wider scanning fields, higher resolution, and improved tissue

141 oupled plasma mass spectrometer coupled to a scanning flow cell, the activity and stability of non-no

142 roscopy techniques, namely cross-correlation scanning fluorescence correlation spectroscopy and numbe

143 surface of individual HIV-1 particles using scanning fluorescence correlation spectroscopy on a supe

144 To this end, using differential scanning fluorimetry and hydrogen-deuterium exchange mas

145 g temperatures derived from the differential scanning fluorimetry experiments indicated a significant

146 Differential scanning fluorimetry showed interaction of the isolated

147 y-multi-angle light scattering, differential scanning fluorimetry, and isothermal calorimetry, to cha

148 ne-based electrophysiology, and differential scanning fluorometry were used to characterize Na(+) and

149 effectively increases the efficiency of TCR scanning for antigen before the T cell is committed to a

150 car (55%) or fovea (16%), and posterior pole scanning for new tumors (11%).

151 For this, we used a scanning force microscope that makes detailed, topograph

152 gressively matures on the target mRNA from a scanning form into an effector mRNP particle by sequenti

153 nt laser produced plasma (LPP) source with a scanning-free GEXRF setup, providing a large solid angle

154 (68)Ga-PSMA PET/CT scanning has been shown to be more sensitive than conven

155 Through alanine scanning, immunofluorescence cell staining and co-immuno

156 It does not need any scanning in the spectral, spatial or polarization dimens

157 oach of atomic force microscopy and vertical scanning interferometry, we quantify the difference in r

158 Recently, we described potentiometric-scanning ion conductance microscopy (P-SICM) for ion-con

159 ng probe nanopipet that enables simultaneous scanning ion conductance microscopy (SICM) and scanning

160 Scanning ion conductance microscopy (SICM) is a nanopipe

161 ons supplied by intact axons identified with scanning ion conductance microscopy in primary hippocamp

162 by a secondary ion mass spectrometry (SIMS) scanning ion image technique (SII).

163 The optimal time for scanning is 144 h after injection.

164 We confirmed that (18)F-FDG PET scanning is a reliable tool for BMI assessment in HL, an

165 patially resolved infrared spectroscopy, and scanning Kelvin probe microscopy are used to investigate

166 Here, the use of an obliquely scanning laser eliminates the z-stacking process, then a

167 d growth occur upon heating and ahead of the scanning laser focus.

168 is paper, we present a method termed oblique scanning laser microscopy (OSLM) to combine optical cohe

169 ch as optical coherence tomography, confocal scanning laser ophthalmoscopy, or scanning laser perimet

170 , confocal scanning laser ophthalmoscopy, or scanning laser perimetry, to measure structure quantitat

171 Proof of principle for the potential of scanning LC-FAIMS-MS in omics applications is demonstrat

172 Overall, (68)Ga-PSMA PET/CT scanning led to a change in planned management in 51% of

173 Imaging with an adaptive optics scanning light ophthalmoscope (AOSLO) enables direct vis

174 tine Cr2Ge2Te6 atomic layers, as revealed by scanning magneto-optic Kerr microscopy.

175 itudinal resolutions of images under various scanning methods.

176 MSM) levels and visualized by confocal laser scanning microscope before being characterized by protei

177 ly integrated into standard two-photon laser-scanning microscopes to generate an axially elongated Be

178 tons imaged with time-lapse two-photon laser scanning microscopy (2PLSM).

179 stered volumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of stained

180 Confocal laser scanning microscopy (CLSM) showed that the number of fun

181 of sectioned specimens under confocal laser scanning microscopy (CLSM).

182 he application of newly developed helium ion scanning microscopy (HIM) to examine the glomerulopathy

183 using in situ zymography and confocal laser scanning microscopy after 24 h or 1-y storage in artific

184 Through confocal laser scanning microscopy and flow cytometry analysis, we demo

185 urthermore, in situ real-time confocal laser scanning microscopy imaging reveals the dynamic process

186 d in the intestine through multiphoton laser scanning microscopy in an ex vivo intestinal model.

187 Two-photon laser scanning microscopy of calcium dynamics using fluorescen

188 ation, immunofluorescence and confocal laser scanning microscopy showed virus replication significant

189 Here, Embon et al. use a unique scanning microscopy technique to image steady-state pene

190 nning electron or three-dimensional confocal scanning microscopy.

191 a protein matrix as shown by confocal laser scanning microscopy.

192 es at higher resolutions than confocal laser scanning microscopy.

193 lky secondary structures, indicating a dsRNA scanning mode of TRBP.

194 A leaky-scanning model of translation based on Kozak translation

195 ificity of antibodies was studied by homolog-scanning mutagenesis (HSM) with single human domain huma

196 Here we used a scanning mutagenesis approach to identify residues in th

197 In this work, we performed alanine scanning mutagenesis of aromatic residues located in tra

198 l analyses, peptide binding analysis, linker-scanning mutagenesis, and nuclear magnetic resonance (NM

199 Alanine scanning mutation of Epep revealed residues critical for

200 Using scanning nanothermometry with submicrokelvin sensitivity

201 GPs have been visualized by scattering-type scanning near-field optical microscopy (s-SNOM), the rea

202 IGNA PET/MR was examined during simultaneous scanning of aggressive MR pulse sequences.

203 Finally, alanine scanning of CDR1 and CDR2 sequences of TRBV4-1 revealed

204 er the entire field of view without any beam scanning or imaging reconstruction.

205 tions, i.e. image distortions, we use spiral scanning paths, allowing precise control of a sub-A size

206 ensor By integrating the microbiosensor in a scanning photoelectrochemical microscope, it was capable

207 e present the development and application of scanning photoelectrochemical microscopy (SPECM) for the

208 whole-cell patch-clamp recordings with laser-scanning photostimulation and performed unsupervised clu

209 Recent developments in scanning probe block copolymer lithography (SPBCL) enabl

210 of a versatile and low-cost electrochemical-scanning probe microscope (EC-SPM) is presented.

211 Here, the authors demonstrate that a scanning probe microscope tip can be used to manipulate

212 ace-based environment and the utilisation of scanning probe microscopies as a primary characterisatio

213 This review gives an overview of using Scanning Probe Microscopy (SPM), in particular Scanning

214 nce microscopy (SICM) is a nanopipette-based scanning probe microscopy technique that utilizes the io

215 Using multifrequency scanning probe microscopy, collagen elastic modulus was

216 ies of these processes have been revealed by scanning probe microscopy.

217 A multifunctional dual-channel scanning probe nanopipet that enables simultaneous scann

218 topological defect-driven magnetic writing-a scanning probe technique-provides access to all of the p

219 The covalent linkages are visualized by scanning probe techniques with submolecular resolution,

220 In motion, the scanning probe tip thereby deterministically reconfigure

221 ere, we report the design and fabrication of scanning probe tips that combine SECM with atomic force

222 fabricated, picowatt-resolution calorimetric scanning probes, we measured the thermal conductance of

223 zed the strong anisotropic behavior of BP by scanning Raman microscopy providing an accurate method f

224 who had positive (68)Ga-HBED-PSMA-11 PET/CT scanning results and underwent comparative (68)Ga-THP-PS

225 Alanine scanning revealed that hydrophobic amino acids in the fi

226 vide molecular mechanisms for stochastically scanning, rewiring, and recycling genetic information on

227 An unbiased alanine-scanning screen covering the entire region combined with

228 o-Raman spectroscopy, Transmission (TEM) and Scanning (SEM) Electron Microscopy on Focused Ion Beam f

229 ively with how high subjects felt during the scanning session.

230 Furthermore, large-area mask-projection scanning stereolithography demonstrates the scalability

231 oliated black phosphorus using confocal fast-scanning technique at different time intervals.

232 ture phenomena revealed by atomic-resolution scanning TEM (STEM) and single-crystal diffraction using

233 device sensitivity and/or the requirement of scanning the detection system to form an image.

234 aptured for the first time a DNA glycosylase scanning the genome for a damaged base in the very first

235 By scanning the newly found data set from RNA-seq, scientis

236 By scanning the spectrum within the characteristic absorpti

237 ucose (n = 305) positron emission tomography scanning to assess amyloid accumulation and brain hypome

238 protein reconstruction with deep mutational scanning to characterize alternative histories in the se

239 ED/RESOLFT nanoscopy through restricting the scanning to subdiffraction-sized regions.

240 We have used the novel environmental scanning transmission electron microscope (ESTEM) with 0

241 esolution imaging in an aberration-corrected scanning transmission electron microscope (STEM) can ena

242 anning electron microscope (SEM) imaging and scanning transmission electron microscope (STEM) tomogra

243 Here we use in situ heating in a scanning transmission electron microscope to observe the

244 c force microscopy (AFM) and high-resolution scanning transmission electron microscopy (HR-STEM) indi

245 udied by scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM) and ene

246 als with low defect density, as confirmed by scanning transmission electron microscopy (STEM) measure

247 orrelative light microscopy and liquid-phase scanning transmission electron microscopy (STEM) were us

248 urements, atomic force microscopy (AFM), and scanning transmission electron microscopy (STEM), we obs

249 Scanning transmission electron microscopy and energy-dis

250 Aberration-corrected scanning transmission electron microscopy and energy-dis

251 and characterizing structures by correlating scanning transmission electron microscopy imaging and CO

252 Operando scanning transmission electron microscopy observations o

253 Atomic-resolution scanning transmission electron microscopy reveals an int

254 n, photoluminescence, and annular dark-field scanning transmission electron microscopy to determine t

255 Scanning transmission electron microscopy was used at su

256 nalyzed by electron backscatter diffraction, scanning transmission electron microscopy, high resoluti

257 Using aberration-corrected scanning transmission electron microscopy, it is found t

258 First, using environmental scanning transmission electron microscopy, we monitor th

259 ion electron microscopy, and high-resolution scanning transmission electron microscopy.

260 ture of the stacking boundary is revealed by scanning transmission electron microscopy.

261 ce (mu-XRF), X-ray diffraction (mu-XRD), and scanning transmission X-ray microscopy (STXM) computed t

262 Complementary scanning transmission X-ray microscopy revealed that the

263 patterned into 1 microm diameter dots, using scanning transmission x-ray microscopy.

264 , we apply in situ, and aberration-corrected scanning, transmission electron microscopy to examine de

265 ecule on a Ag(110) surface using a cryogenic scanning tunneling microscope (STM).

266 110) by combining supersonic molecular beam, scanning tunneling microscopy (STM), and ab initio molec

267 anning Probe Microscopy (SPM), in particular Scanning Tunneling Microscopy (STM), to study the change

268 Using high resolution scanning tunneling microscopy and spectroscopy (STM/STS)

269 ing an alternative approach, which relies on scanning tunneling microscopy and spectroscopy, we prepa

270 (110) at 4.6 K was studied experimentally by scanning tunneling microscopy and theoretically by molec

271 arge signal amplitudes have been revealed by scanning tunneling microscopy in intercalated van der Wa

272 all-angle X-ray scattering and complementary scanning tunneling microscopy measurements.

273 In situ scanning tunneling microscopy reveals not only their mol

274 We used scanning tunneling microscopy to study low-angle grain b

275 iquid interface was investigated by means of scanning tunneling microscopy, allowing imaging of the m

276 ort of small molecules is measured well with scanning tunneling microscopy, conducting atomic force m

277 ay photoelectron spectroscopy, high-pressure scanning tunneling microscopy, high-pressure surface X-r

278 -charge-density-wave insulator 1T-TaS2 using scanning tunneling spectroscopy.

279 tial periodicity below TDW from diffraction, scanning tunnelling and photoemission based probes sugge

280 polymers assisted by hole injections from a scanning tunnelling microscope (STM) tip.

281 pectral distribution of light emitted from a scanning tunnelling microscope junction not only bears i

282 d a point-like top gate made by decorating a scanning tunnelling microscope tip with a gold nanowire.

283 ing scheme to uncover, in conjunction with a scanning tunnelling microscope tip-assist, a hidden equi

284 riodicity is given by kF/pi, consistent with scanning tunnelling microscopy and angle resolved photoe

285 Scanning tunnelling microscopy and atomic manipulation c

286 Here we use numerical simulations and scanning tunnelling microscopy data to show that these r

287 Scanning tunnelling microscopy enables individual rotors

288 Here we show by spin-resolved scanning tunnelling microscopy that the spin direction a

289 Scanning tunnelling microscopy together with density fun

290 Here we use scanning ultrafast electron microscopy to image the dyna

291 n=17) and without (n=20) ADHD completed fMRI scanning under each of three conditions: (a) smoking as

292 ents with MDD (HDRS-24 = 24.8) underwent PET scanning using (11)C-DASB.

293 Results Mean heart rate during scanning was 83 beats per minute +/- 21 (standard deviat

294 Furthermore, rapid, repetitive scanning was done, which allowed measurement of contrast

295 The 3D scanning was performed 0, 1, 3, 5, and 10 min after ligh

296 hy (DSA) of cerebral vessels with rotational scanning was performed.

297 ess (after accounting for age at the time of scanning) was associated with reduced cortical thickness

298 ithout prior local therapy and (18)F-FET PET scanning were retrospectively identified in 2 centers.

299 re, the shelf life of more than 24 h and the scanning window of at least 3 h make (64)Cu-DOTATATE fav

300 d sensitivity was stable during simultaneous scanning within 0.3%.