ライフサイエンスコーパス: microscopy

1 ular location in the plastid by fluorescence microscopy.

2 of the nucleus, as shown by super-resolution microscopy.

3 on is imaged by single-particle fluorescence microscopy.

4 immunohistochemistry and immunofluorescence microscopy.

5 mages are acquired with automated time-lapse microscopy.

6 as analyzed by using structured illumination microscopy.

7 ructured dodecamer as visualized by electron microscopy.

8 ture, using SEM, light and immunofluorescent microscopy.

9 s well as scanning electron and atomic force microscopy.

10 titated using confocal and scanning electron microscopy.

11 d two PSII monomers as deduced from electron microscopy.

12 determined by single-particle electron cryo-microscopy.

13 orescence-lifetime imaging microscopy (FLIM) microscopy.

14 ry cortices using three-dimensional electron microscopy.

15 sily tracked over 72 h via standard confocal microscopy.

16 ing 185 smears (50.4%) that were positive by microscopy.

17 the structure identified by super-resolution microscopy.

18 signal to noise ratio of localisation based microscopy.

19 e orientation with fluorescence polarization microscopy.

20 iffraction and aberration corrected electron microscopy.

21 gh-speed non-contact lateral molecular force microscopy.

22 crease in surface roughness evident by force microscopy.

23 y focused ion-beam milling scanning electron microscopy.

24 for 2.5 min was shown by immunofluorescence microscopy.

25 rived from stochastic optical reconstruction microscopy.

26 n affinity fluorescence and super-resolution microscopy.

27 n was studied by flow cytometry and confocal microscopy.

28 dra2, a well-known PAFP used in localization microscopy.

29 cellular level using immunofluorescence and microscopy.

30 ofluorescence microscopy, and immunoelectron microscopy.

31 3 K for 8-360 hours and analyzed by electron microscopy.

32 aphy (CT), autoradiography, and fluorescence microscopy.

33 namic light scattering and scanning electron microscopy.

34 myeloid leukemia using intravital two-photon microscopy.

35 on of F-actin in Li1 plant cells by confocal microscopy.

36 es and high resolution transmission electron microscopy.

37 investigations were performed using confocal microscopy.

38 e transfer of BMDCs was examined by means of microscopy.

39 fibril formation using transmission electron microscopy.

40 , superresolution, and transmission electron microscopy.

41 family as novel probes for super-resolution microscopy.

42 ion of 1) single-objective based light-sheet microscopy, 2) photoconvertible proteins, and 3) fluores

43 der two-photon fluorescence lifetime imaging microscopy (2pFLIM).

44 nting this method in secondary electron (SE) microscopy, a SE spectrum (white electrons) associated w

45 an be imaged and analysed using mobile phone microscopy, achieving a new milestone for tele-medicine

46 l-channel two-photon fluorescence anisotropy microscopy acquisition to perform drug-target measuremen

47 he nanometer-scale radius of an atomic force microscopy (AFM) tip yields a very low signal-to-noise r

48 ispersive X-ray analysis (EDX), atomic force microscopy (AFM), scanning electron microscopy (SEM), UV

49 ere explored in live cells with atomic force microscopy (AFM).

50 investigated by means of scanning tunneling microscopy, allowing imaging of the molecular structure

51 for PAM in biomedical sciences.Photoacoustic microscopy allows for label-free 3D in vivo imaging by d

52 urements and images obtained by atomic force microscopy also demonstrated the dissociation of the PCN

53 s spectrometry, flow cytometry, and electron microscopy analyses indicated that Cavin-2 is secreted i

54 Finally, transmission electron microscopy analysis revealed the effect of the interface

55 ession of GCaMP6s, combined with light sheet microscopy and a novel image processing pipeline, for th

56 We present a combination of optical microscopy and AFM-IR imaging to characterize OM heterog

57 amined by scanning and transmission electron microscopy and by staining of filamentous actin.

58 Advances in fluorescence microscopy and calcium sensitive dyes has led to the rou

59 enitors using image patches from brightfield microscopy and cellular movement.

60 Using fluorescence microscopy and cryo-electron tomography, we showed that

61 sits were characterized using confocal laser microscopy and electrochemical methods.

62 We present chemical (scanning electron microscopy and electron microprobe) and structural (elec

63 embly, we carried out real-time atomic force microscopy and electron microscopy studies.

64 Using fluorescence microscopy and electron tomography, we find that centrio

65 mbination of 3-DISCO technique with 1-photon microscopy and epifluorescence microscopy under high pow

66 s of acute leukemia, we used high-resolution microscopy and flow cytometry to highlight the heterogen

67 diffusion of the mobile lo domains by video microscopy and particle tracking showed that the domains

68 rful tools for super-resolution localization microscopy and protein tagging.

69 g stage for automated high-content screening microscopy and provide detailed step-by-step instruction

70 Fluorescence microscopy and quantitative reverse transcription polyme

71 Despite an extensive microscopy and radiography network at middle levels of t

72 and samples collected for scanning electron microscopy and RNA sequencing.

73 The transmission electron microscopy and selected-area electron diffraction confir

74 Offline microscopy and spectroscopy studies have shown that dry

75 s difficult to obtain quantitative data from microscopy and subcellular fractionation is experimental

76 imilar measurements by confocal fluorescence microscopy and subcellular fractionation of endocytic ve

77 directions of tip-enhanced near-field Raman microscopy and TERS.

78 determined by single-particle cryo-electron microscopy and validation of the structure using footpri

79 Single-vesicle optical (by TIRF microscopy) and biophysical measurements of ATP release

80 grees , C *, DeltaE) microstructure (optical microscopy), and ascorbic acid (AA) degradation kinetics

81 novel tissue-clearing technique, lightsheet microscopy, and automated registration by image analysis

82 we used quantitative live-cell fluorescence microscopy, and compared the effects of the DAT inhibito

83 to copper joints using transmission electron microscopy, and found a 10 nm thick transition layer co

84 emical tools, development of high-resolution microscopy, and identification of centriole components h

85 rmed by Western blotting, immunofluorescence microscopy, and immunoelectron microscopy.

86 pproaches (non-invasive imaging, 3D-electron microscopy, and mathematical modelling) to show that phl

87 ive-cell imaging, correlative light electron microscopy, and single-cell analysis, we found that afte

88 te, their locations determined using optical microscopy, and the cell locations used to guide the acq

89 Here the authors use fluorescence microscopy approaches to directly visualize and investig

90 cial marks for single particle cryo-electron microscopy approaches.

91 ge fusion specific to SIMS-based correlative microscopy are discussed in detail alongside the advanta

92 eparation and data acquisition with confocal microscopy are simple and fast, the method can serve as

93 onment and the utilisation of scanning probe microscopies as a primary characterisation tool are high

94 Using confocal and electron microscopy as well as mathematical analyses, we examined

95 thioflavin T staining, transmission electron microscopy, as well as ion mobility-mass spectrometry co

96 l investigations using transmission electron microscopy at various locations to reveal the origins of

97 e present an imaging system for localisation microscopy based on non-destructive readout camera techn

98 ological profiling of cDNA constructs, via a microscopy-based Cell Painting assay.

99 Fluorescence microscopy-based in vitro reconstitution assays reveal t

100 At the concentrations used in cryo-electron microscopy, Bim1 causes the compaction of yeast microtub

101 content and collection-efficiency boosts in microscopy, but efficient implementations for macroscopi

102 erular diseases characterized on fluorescent microscopy by C3 accumulation with absent, or scanty, im

103 using a conventional conductive atomic force microscopy (CAFM) without a top electrode is not feasibl

104 subjected to an in-depth analysis by optical microscopy, calorimetry and small angle X-ray scattering

105 ss spectrometry and high resolution electron microscopy can define the subunit topology and copper bi

106 In vivo confocal microscopy can help in this challenging diagnosis, espec

107 catter diffraction and transmission electron microscopy) characterization of the recovered phases and

108 lumetric fluorescent confocal laser scanning microscopy (CLSM) images (z-stacks) of stained cells and

109 Confocal laser scanning microscopy (CLSM) showed that the number of fungal cells

110 Here, we used electron microscopy combined with genetic labeling to define the

111 Motorized fluorescence microscopy combined with high-throughput microfluidic ch

112 ircular dichroism spectroscopy, and electron microscopy; compared the properties of the recombinant p

113 ite recording from pure axonal branches in a microscopy-compatible environment.

114 Confocal and scanning electron microscopy confirm removal of biofilm matrix components

115 ach to cryogenic photoactivated localization microscopy (cPALM) that permits the use of a room-temper

116 We determined electron cryo-microscopy (cryo-EM) and crystal structures of unbound a

117 this work, we demonstrate that cryo-electron microscopy (cryo-EM) can be used to image nanoscale lipi

118 nt advances in single-particle electron cryo-microscopy (cryo-EM) data processing allowing for the ra

119 Cryo-electron microscopy (cryo-EM) had played a central role in the st

120 macromolecular structures into cryo-electron microscopy (cryo-EM) maps is a major challenge, as the m

121 ere, we report high resolution cryo electron microscopy (cryo-EM) maps of wild type CPMV containing R

122 h we present a high-resolution cryo-electron microscopy (cryo-EM) structure of the core tetrameric HI

123 precipitated with tyrosinase, while confocal microscopy demonstrated colocalization of the proteins.

124 Fluorescence microscopy demonstrated intense labelling of non-ghost a

125 Analytical microscopy demonstrated internalization and dissolution

126 Immunogold electron microscopy demonstrated that E4 34K is located at a sing

127 e of this complex by negative stain electron microscopy, demonstrating that two copies of VirD4 dimer

128 thin films by ultrafast transient absorption microscopy, demonstrating three distinct transport regim

129 n, and nucleator deficiency, consistent with microscopy-derived models proposing PMS as specialized c

130 Despite progress in super-resolution microscopy, discriminating and quantifying these process

131 ) were characterized using scanning electron microscopy, dynamic light scattering, and zeta potential

132 Using light-sheet microscopy, early neural development is here followed in

133 cipher neuronal circuits, including electron microscopy (EM) and light microscopy (LM).

134 On virions, electron microscopy (EM) and tomography reveal monomeric spikes s

135 Progress in 3D electron microscopy (EM) imaging has greatly facilitated neurosci

136 Rad26 heterotetrameric complex with electron microscopy enabled me to propose a structural model for

137 gain in resolution over traditional optical microscopy, enabling the localization of individual mole

138 Reflectance confocal microscopy enhanced the diagnosis of pigmented facial ma

139 lution of ultrafast electron diffraction and microscopy experiments is currently limited by the avail

140 Fluorescence microscopy experiments showed that I2 colocalized with a

141 photoelectron spectroscopy and atomic force microscopy experiments.

142 This result was confirmed by confocal microscopy experiments.

143 For instance, fluorescence microscopy faces a 'colour barrier', owing to the intrin

144 the overall sensitivity of in vivo confocal microscopy features of AK is low.

145 in cells using fluorescence-lifetime imaging microscopy (FLIM) microscopy.

146 all suitable specimens for detecting fungi; microscopy, fungal culture, galactomannan antigen, and a

147 and CuPc films are analyzed by atomic force microscopy, grazing incident X-ray diffraction, X-ray ph

148 Atomic force microscopy, high-resolution flow cytometry, real-time qu

149 The Electron Microscopy Hole Punch (EMHP) is a streamlined suite of t

150 zed by high resolution transmission electron microscopy (HRTEM), energy dispersive X-ray analysis (ED

151 Here we present high-speed atomic force microscopy (HS-AFM) observations of membrane-reconstitut

152 We obtained 3-D electron microscopy images of podocytes and used quantitative fea

153 Confocal fluorescence microscopy images of the perpendicular and parallel brai

154 Confocal microscopy images showed that the intensity of the green

155 ation analysis and Fourier transformation of microscopy images.

156 By combining Kelvin probe force microscopy imaging and phase-field simulations, we show

157 tion and sensitivity for a range of electron microscopy imaging modalities, including, for example, s

158 e, in situ real-time confocal laser scanning microscopy imaging reveals the dynamic process of gNP ag

159 ss spectrometry analyses as well as electron microscopy imaging.

160 electrocardiography, and magnetic resonance microscopy imaging.

161 Using confocal laser and scanning electron microscopy, immunofluorescence, and live-cell imaging, o

162 Time-lapse two-photon microscopy in adult slices was used to determine the pre

163 intestine through multiphoton laser scanning microscopy in an ex vivo intestinal model.

164 sing superresolution structured illumination microscopy in conjunction with both pharmacological and

165 scence correlation spectroscopy and electron microscopy in live cells, we show that G12V K-Ras exists

166 prisms, enabled by nanometer-scale real-time microscopy in solution, shows a transition from an early

167 y transforming stimulated emission depletion microscopy into a time-resolved ultrafast approach, we m

168 Microscopy investigations revealed the transformation of

169 Forster resonance energy transfer (FRET) microscopy is a powerful technique capable of investigat

170 t near-atomic resolution using cryo-electron microscopy, is strikingly similar to that observed in ds

171 As an extension of wide-field fluorescence microscopy, it is inherently capable of multicolor imagi

172 as revealed by fluorescence lifetime imaging microscopy, leading to integrin-mediated phosphorylation

173 including electron microscopy (EM) and light microscopy (LM).

174 ectrophoretic manipulation with fluorescence microscopy making use of their fluorescence emission in

175 arison with a 7.8 A resolution cryo-electron microscopy map of a Mediator-RNA polymerase II holoenzym

176 A recently reported 9-A cryo-electron microscopy map of the Tetrahymena telomerase holoenzyme

177 ttering and complementary scanning tunneling microscopy measurements.

178 this segment determined by the cryo-electron microscopy method micro-electron diffraction explain its

179 A novel time-lapse synchrotron deep-UV microscopy methodology was developed that made use of th

180 field that is inaccessible to other optical microscopy methods can be obtained.

181 demonstrate microtomy-assisted photoacoustic microscopy (mPAM) of mouse brains and other organs, whic

182 ,318 were tested for malaria infection using microscopy (n = 131,652) or RDT (n = 138,540).

183 llection increased tuberculosis diagnosis by microscopy (odds ratio [OR] 1.6, 95% CI 1.3-1.9, p<0.000

184 sis of recombinant protein and electron cryo-microscopy of acidified hantavirus allows us to propose

185 Moreover, transmission electron microscopy of glomeruli and immunofluorescent staining o

186 Utilizing multi-color TIRF microscopy of in vitro reconstituted F-actin networks, w

187 was also apparent from transmission electron microscopy of infected cells.

188 Here we use four-dimensional confocal microscopy of live animals to observe changes to spermat

189 capsidating nucleoprotein, and cryo-electron microscopy of nucleocapsid or nucleocapsid-like structur

190 Serial block face scanning electron microscopy of zebrafish cones revealed that nearly 100 m

191 Super-resolution microscopy offers a significant gain in resolution over

192 Single-molecule-based super-resolution microscopy offers researchers a unique opportunity to qu

193 ciparum CSP, we used negative-stain electron microscopy on a recombinant shortened CSP (rsCSP) constr

194 Here, we combine advanced spectroscopy and microscopy on model Pd/C samples to decouple the electro

195 e not apparent through transmission electron microscopy or limited proteolysis.

196 sistance increased diagnostic performance by microscopy (OR 1.6, 95% CI 1.3-2.0, p<0.0001).

197 either histological sections imaged by light microscopy, or electron micrographs of single ultrathin

198 ibed potentiometric-scanning ion conductance microscopy (P-SICM) for ion-conductance measurement in p

199 gy and urine POC-CCA testing detected all 23 microscopy-positive study participants (100% sensitivity

200 ) for use as a dual scanning electrochemical microscopy probe.

201 Spontaneous Raman microscopy probes vibrational transitions with much narr

202 X-ray fluorescence (XRF) microscopy, quantified with elemental correlation densit

203 In this study, we used multispectral microscopy, quantitative pathology, and gene expression

204 der X-ray diffraction, transmission electron microscopy, Raman and wavelength/energy dispersive X-ray

205 aracterizations (X-ray diffraction, electron microscopy, Raman, and UV-visible spectroscopies).

206 Reflectance confocal microscopy (RCM) improves diagnostic accuracy for LM and

207 In light microscopy, refractive index mismatches between media an

208 at look amorphous and disordered by electron microscopy, reminiscent of the reported formation of amo

209 labeling approach to structured illumination microscopy resulted in an increase in resolution, highli

210 Secretome-wide predictions and confocal microscopy reveal that rust fungi might have evolved mul

211 In failing myocardium, confocal laser microscopy revealed alpha-B crystallin in subsarcolemmal

212 In addition, microscopy revealed rapid restoration of bladder integri

213 -3 treated matrices by transmission electron microscopy revealed remodelling and degradation of core

214 Field emission scanning electron microscopy revealed that ethanol solutions of 3 form flo

215 Cryo-electron microscopy reveals the structure of a chloride channel t

216 iously reported for scanning electrochemical microscopy (SECM) imaging of molecular microarrays.

217 cancer cells using scanning electrochemical microscopy (SECM).

218 ostructures are studied by scanning electron microscopy (SEM), scanning transmission electron microsc

219 ic force microscopy (AFM), scanning electron microscopy (SEM), UV-Vis spectroscopy, X-ray diffraction

220 k material was analyzed by Scanning Electron Microscopy (SEM), X-ray-tomography and Fourier-Transform

221 ing Ultra-Microtome (ATUM) Scanning Electron Microscopy (SEM).

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

223 8 mum can be observed from scanning electron microscopy (SEM).

224 ges of the template obtained by atomic force microscopy show that TFAM creates loops in a discrete re

225 the surface of S. epidermidis, and electron microscopy showed cellular aggregates connected by discr

226 Atomic Force Microscopy showed significant alterations to the surface

227 Confocal fluorescence microscopy showed that a fraction of HCF222-green fluore

228 Photoinduced force microscopy shows that doping level can be optically modu

229 Scanning ion conductance microscopy (SICM) is a nanopipette-based scanning probe

230 f optical sectioning structured illumination microscopy (SIM), we have captured high-resolution 3D im

231 Round morphology (by transmission electron microscopy), size ( approximately 180 nm diameter by nan

232 unfolding using single molecule atomic force microscopy (smAFM) and steered molecular dynamics (SMD)

233 used to perform single-molecule localization microscopy (SMLM) on cells expressing mCherry, which ren

234 oscopy (SEM), scanning transmission electron microscopy (STEM) and energy dispersive X-ray spectrosco

235 upersonic molecular beam, scanning tunneling microscopy (STM), and ab initio molecular dynamics.

236 In a recent cryo-electron microscopy structure of chicken Slo2.2, the ion permeati

237 Here, we report the cryo-electron microscopy structure of full-length ZntB from Escherichi

238 Here, we report the cryo-electron microscopy structure of mature Japanese encephalitis vir

239 re we present the 3.0 angstrom cryo-electron microscopy structure of mTORC1 and the 3.4 angstrom stru

240 substrate (casein), we report cryo-electron microscopy structures at near-atomic resolution of Hsp10

241 ere we present high-resolution cryo-electron microscopy structures of subtype B B41 SOSIP Env trimers

242 Transmission electron microscopy studies demonstrate that single molecules are

243 al-time atomic force microscopy and electron microscopy studies.

244 present study we applied array tomography, a microscopy technique that combines ultrathin sectioning

245 (SICM) is a nanopipette-based scanning probe microscopy technique that utilizes the ionic current flo

246 Here, we translate 3D-microscopy techniques (focused ion beam nanotomography,

247 While transmission electron microscopy (TEM) and operando X-ray absorption spectrosc

248 Transmission electron microscopy (TEM) revealed that TFV and ADV-treated HK-2

249 le-ICP-MS (sp-ICP-MS), Transmission Electron Microscopy (TEM), Analytical Ultracentrifugation (AUC),

250 Using immuno-transmission electron microscopy (TEM), we observed that a large number of int

251 hin sections imaged by transmission electron microscopy (TEM).

252 tion FFF or SdFFF) and transmission electron microscopy (TEM).

253 the GJs are structures observed by electron microscopy termed the electrical synapse density (ESD) [

254 Traction force microscopy (TFM) revealed that cells produced the greate

255 is was made possible not only by advances in microscopy that helped answer questions about cell biolo

256 we show by spin-resolved scanning tunnelling microscopy that the spin direction at the surfaces of bu

257 Using conducting tip atomic force microscopy, the energies of {Co9(P2W15)3} frontier molec

258 specific interaction between an atomic force microscopy tip decorated with recombinant alphaIIbbeta3

259 vitro total internal reflection fluorescence microscopy (TIRFM) and kinetic and thermodynamic measure

260 Here, we employed high-resolution confocal microscopy to analyze nuclear morphology and F-actin rea

261 We used high-precision time-lapse microscopy to characterize the maturation kinetics of 50

262 lecular dynamics simulation and atomic force microscopy to deliver, in atomic detail, structural mode

263 analysed by immunofluorescence and confocal microscopy to determine CR1 cluster number and volume.

264 Here we use high-resolution single-molecule microscopy to directly observe the stepping behavior of

265 Here, we used high-speed atomic force microscopy to directly visualize the membrane-insertion

266 Here we utilize in situ spectroscopy and microscopy to identify and characterize a support effect

267 f RhoA, live-cell imaging and traction force microscopy to investigate the dynamics of actomyosin-bas

268 in both cases using light-sheet fluorescence microscopy to optically access the intestinal bulb of th

269 We use single-cell microscopy to parameterize a full cell-cycle model based

270 In this article, applications of FRET microscopy to protein interactions and modifications are

271 We used serial-section electron microscopy to reconstruct PNS neurons and their hitherto

272 We used scanning tunneling microscopy to study low-angle grain boundaries at the su

273 mbine Nomarski and multichannel fluorescence microscopy to study processes such as cell-fate specific

274 olution to this problem is to use two-photon microscopy to target fluorescently labeled neurons.

275 le proteins, and 3) fluorescence correlation microscopy, to quantitatively measure 3D protein dynamic

276 with 1-photon microscopy and epifluorescence microscopy under high power LED illumination, followed b

277 g pavement cells, was visualized by confocal microscopy using a flavonol-specific fluorescent dye.

278 ized by photoluminescence, scanning electron microscopy, UV-Visible spectra and X-ray diffraction pat

279 Furthermore, in transmission electron microscopy, vesicular structures are observed in connect

280 ), the positive predictive value of confocal microscopy was 87.5% and the negative predictive value w

281 Microscopy was combined with immunodetection with specif

282 mages in situations where conventional Raman microscopy was unable to visualize the sublayer.

283 In parallel, polarized light microscopy was used to observe the microstructure.

284 Confocal microscopy was used to study functional and bioenergetic

285 color total internal reflection fluorescence microscopy, we demonstrate complex formation by showing

286 siae Using cell-free fusion assays and light microscopy, we find that GTPase activation and trans-SNA

287 By using atomic force microscopy, we found that during reverse transcription t

288 replisomes in live E. coli with fluorescence microscopy, we found that the Pol III* subassembly frequ

289 Using confocal microscopy, we observe the initial particle attachment t

290 multiwavelength single-molecule fluorescence microscopy, we observed the dynamics of GreB interaction

291 Using photoactivated localization microscopy, we reveal that the contact area of single ER

292 With single-molecule atomic force microscopy, we show a specific interaction between an at

293 Here, using in situ electron microscopy, we show how gold and silver nanocrystals nuc

294 vitro total internal reflection fluorescence microscopy, we show that bacterial mini microtubules tre

295 immunofluorescent and transmission electron microscopy, we showed that S. pneumoniae rapidly adhered

296 Using electron microscopy, we showed that this peptide physically destr

297 Using atomic force microscopy, we studied the elasticity of mouse myoblasts

298 larly true for super-resolution localization microscopy where high demands are placed especially on t

299 use superresolution structured illumination microscopy with single-particle averaging to localize 14

300 the particles included transmission electron microscopy, X-ray diffraction and asymmetrical flow fiel