ライフサイエンスコーパス: microscopy

1 ation provided by visible light and electron microscopy.

2 ely being used in spectroscopy, sensing, and microscopy.

3 n a salivary rinse sample using fluorescence microscopy.

4 , and imaged by high-resolution atomic force microscopy.

5 sophila genetics and husbandry, and confocal microscopy.

6 letion of intracytoplasmic granules by light microscopy.

7 ects can be studied in real time using video microscopy.

8 changes using single-particle cryo-electron microscopy.

9 py mapping and calibrated Kelvin probe force microscopy.

10 ro-computed tomography and scanning electron microscopy.

11 stituted in lipids optimal for cryo-electron microscopy.

12 aphy was also viewed under scanning electron microscopy.

13 ted live-cell, super-resolution and electron microscopy.

14 pectroscopy, X-ray diffraction, and electron microscopy.

15 ca wafer was characterized with atomic force microscopy.

16 te-of-the-art scanning transmission electron microscopy.

17 Mitochondria were evaluated using electron microscopy.

18 s measured by a method based on atomic force microscopy.

19 , H&E staining, and light-sheet fluorescence microscopy.

20 mer screening, ELISA, and immunofluorescence microscopy.

21 absence of hepcidin solved by cryo-electron microscopy.

22 sts experienced in conventional fluorescence microscopy.

23 gen content and morphology using multiphoton microscopy.

24 receptor expression using immunofluorescent microscopy.

25 assay, structure-based mutants, and advanced microscopy.

26 ic resolution scanning transmission electron microscopy.

27 or glucose analog, and analyzed by confocal microscopy.

28 zed using optical microcopy and atomic force microscopy.

29 nted for visualization using superresolution microscopy.

30 series sectioning for transmission electron microscopy.

31 logic neoplasms had substructure on electron microscopy.

32 erated by serial blockface scanning electron microscopy.

33 solution by non-invasive NIR-IIb light sheet microscopy.

34 l activation by combining fUS and two-photon microscopy (2PM) in a co-registered single voxel brain v

35 lso provide a deeper focus into atomic force microscopy (AFM) applications that can bridge diverse le

36 optical and magnetic tweezers, atomic force microscopy (AFM), single-molecule fluorescence resonance

37 s of the deposits acquired from atomic force microscopy (AFM).

38 nd imaging were performed using atomic force microscopy (AFM).

39 cally patterned substrates with atomic force microscopy (AFM).

40 Further combination with fluorescence microscopy allows users to determine cells or regions of

41 alence of P falciparum infection detected by microscopy, anaemia (study defined values or haemoglobin

42 iochemical approaches and immunofluorescence microscopy analyses, we sought to investigate the mechan

43 Overall, reflection interference contrast microscopy analysis of SCP-biochip interactions revealed

44 ere we perform in situ transmission electron microscopy analysis of the synthesized red-phosphorus-im

45 s and advanced in situ transmission electron microscopy analysis to elucidate the interplay between f

46 y validated by chromatographic mycotoxin and microscopy analysis.

47 ia a combined hydrodynamic size and electron microscopy analysis.

48 ing system using conventional confocal light microscopy and a specialized analysis software to produc

49 ents and analyzed its appearance by electron microscopy and ability to support histone pre-mRNA proce

50 ingle molecule fluorescence, time-lapse TIRF microscopy and AFM imaging we characterize this phenomen

51 in-situ environmental transmission electron microscopy and atomistic simulation, we reveal that the

52 Using cryoelectron microscopy and biochemistry, we show that RIG-I-like rec

53 Scanning electron microscopy and colony forming unit counting are commonly

54 combination of atom-resolved scanning probe microscopy and density functional theory to reveal how t

55 t of tissue-clearing methods and light-sheet microscopy and discuss applications of these techniques

56 maging approaches including super-resolution microscopy and electron microscopy we identified, in adu

57 Furthermore, correlative light-electron microscopy and energy-filtered transmission electron mic

58 Here, fluorescence microscopy and genetics were used to confirm the central

59 her investigated by genetic, high-resolution microscopy and high-throughput co-immunoprecipitation st

60 on of total internal reflection fluorescence microscopy and image correlation spectroscopy to monitor

61 9 angstrom, respectively, with cryo-electron microscopy and image reconstruction methods.

62 tomography, light and transmission electron microscopy and in vivo ophthalmoscopy, we describe the u

63 ing x-ray diffraction, transmission electron microscopy and in-situ small angle neutron scattering.

64 oint edge-excitation sub-diffraction (SPEED) microscopy and its two-dimensional (2D)-to-3D transforma

65 at different time points using fluorescence microscopy and Lactate dehydrogenase (LDH) assay on the

66 Confocal microscopy and molecular and classical microbiology were

67 ubwavelength applications such as near-field microscopy and nanoparticle manipulation.

68 stals, as confirmed by transmission electron microscopy and Raman signatures.

69 Atomic force microscopy and scanning electron microscopy show cluster

70 However, existing methods for linking microscopy and single-cell RNA-seq (scRNA-seq) have limi

71 have been investigated by scanning tunneling microscopy and spectroscopy, complemented by theoretical

72 ths of TB treatment, as well as sputum-smear microscopy and sputum-culture positivity at 2 and 6 mont

73 cholangiocytes, but both immunogold electron microscopy and super-resolution microscopy showed that I

74 Mating experiments, fluorescence microscopy and TEM revealed indigenous bacteria could ob

75 le to that of linear structured illumination microscopy and the axial resolution is similar to that o

76 h the cell morphologies by scanning electron microscopy and the ion-concentration analysis by inducti

77 hesions during cell migration using confocal microscopy and total internal reflection fluorescence mi

78 uctural resolution of Pv-M17 by cryoelectron microscopy and X-ray crystallography together with solut

79 scanning calorimetry (DSC), polarised light microscopy and X-ray diffraction (XRD) techniques.

80 ial scanning calorimetry, polarizing optical microscopy and X-ray diffraction provided insight into t

81 study, we combine microfluidics, time-lapse microscopy, and computational modeling to investigate ho

82 spectroscopy, scanning transmission electron microscopy, and electrical characterization.

83 computed tomography (micro-CT), fluorescence microscopy, and fine root hydraulic conductivity measure

84 ed through UV-VIS spectrometry, SEM, optical microscopy, and light exposure.

85 perspectral imaging, confocal laser scanning microscopy, and nanoparticle-based O(2) imaging, we demo

86 otential, dynamic light scattering, electron microscopy, and other spectroscopic techniques.

87 , stable isotope analysis, scanning electron microscopy, and sediment analyses, we document hundreds

88 attering and environmental scanning electron microscopy, and with porcine mucin as the model mucin sy

89 ties of the 9.4 MHz SPML-OCT system in three microscopy applications.

90 proaches in single molecule spectroscopy and microscopy are able to resolve the spatial and temporal

91 pathways obtained using in situ atomic force microscopy are also discussed.

92 Advances in cryo-electron microscopy are enabling increasingly elaborate sub-compl

93 scence, and analytical transmission electron microscopies as well as stable isotope labeling.

94 s assessed employing confocal laser scanning microscopy as well as confocal Raman microspectroscopy.

95 ese isoforms were studied using atomic force microscopy at high resolution in air and buffer.

96 ng in the infrared and highlight an electron-microscopy-based approach for probing complex-shaped nan

97 Finally, microscopy-based metabolic analysis revealed that migrat

98 Here, we developed a high-throughput microscopy-based retrotransposition assay that identifie

99 vative was studied by the scanning tunneling microscopy break-junction method.

100 g-incidence wide-angle X-ray scattering, and microscopy can be related directly to device degradation

101 croscopy who get basic training in dual-beam microscopy can complete the protocol within 2-3 d, allow

102 Fluorescence microscopy can provide extensive information about these

103 s, cell transfection, Western blot, confocal microscopy, cell degranulation, prostaglandin D(2) secre

104 microscopy (SEM) and confocal laser scanning microscopy (CLSM) confirmed that TPI played an important

105 lied cryogenic correlated light and electron microscopy, combined with electron cryo-tomography, to i

106 Here, we use high-resolution microscopy, computational modeling, and in vitro and in

107 t achieves synchronous fluorescence-electron microscopy correlation.

108 puted tomographic imaging, scanning electron microscopy, corrosion casting, and direct multiplexed me

109 Transmission electron microscopy coupled with energy dispersive X-ray spectros

110 Cryo-electron microscopy (cryo-EM) images show that new aggregates pro

111 ization using a time course of electron cryo-microscopy (Cryo-EM) imaging reveals a crystalline inter

112 on results with the results of cryo-electron microscopy (cryo-EM) reconstruction of multiple 3D DNA o

113 Moreover, a 3.4 angstrom cryo-electron microscopy (cryo-EM) structure of a neutralizing monoclo

114 The 4 angstrom resolution cryoelectron microscopy (cryo-EM) structure of gammaTuRC, combined wi

115 Here, we report the cryo-electron microscopy (cryo-EM) structure of Homo sapiens CHD4 enga

116 era enabled us to determine the cryoelectron microscopy (cryo-EM) structure of the channel functional

117 Here, we report the cryoelectron microscopy (cryo-EM) structures of DNA-PKcs (DNA-PK cata

118 Here, we present cryo-electron microscopy (cryo-EM) structures of translationally inact

119 Here, we present two cryoelectron microscopy (cryo-EM) structures of UCN1-bound CRF1R and

120 High-resolution cryoelectron microscopy (cryo-EM) structures reveal that the binding

121 the nucleosome, generated using cryoelectron microscopy (cryo-EM), cross-linking mass spectrometry, a

122 Using cryoelectron microscopy (cryo-EM), we resolved the first three-dimens

123 termined their structure using cryo-electron microscopy (cryo-EM).

124 onance (NMR) imaging, and cryogenic electron microscopy (cryo-EM).

125 Cryogenic transmission electron microscopy (cryo-TEM) revealed key differences in the na

126 Here we report a cryo-electron microscopy (cryoEM) structure of PDE6 complexed to GTP-b

127 turbation of gene expression, acquisition of microscopy data and image analysis can be completed with

128 trary to commonly used experimental methods, microscopy data are fast processed, in less than 1 h.

129 ree-dimensional single-molecule localization microscopy datasets.

130 Scanning electron microscopy demonstrated particle sizes of 3-100 mum.

131 Immunoelectron microscopy demonstrates myelination of the graft-derived

132 The state-of-the-art microscopy directly images atomic/molecular configuratio

133 Field-emission scanning electron microscopy elucidated the morphology of the subpopulatio

134 Here we present cryo-electron microscopy (EM) data resolving the EC1 and EC1+2 domains

135 fast development of high-resolution electron microscopy (EM) demands a background-noise-free substrat

136 Large field epifluorescence microscopy enabled in situ and real-time tracking of Bac

137 erised by dynamic light scattering, electron microscopy, encapsulation efficiency, and drug loading c

138 nt to single-cell occupancies quantified via microscopy, establishing robust droplet screening at sin

139 ge growth rates can be inferred from DSC and microscopy experiments which could be used to guide mole

140 xceeded 100 U.kg(-1), determined by confocal microscopy, extractability and free sulfhydryl assays.

141 rised using field emission-scanning electron microscopy (FE-SEM) and cyclic voltammetry (CV).

142 aberrometry, and biomechanical and confocal microscopy findings.

143 Fluorescence lifetime imaging microscopy (FLIM) is a key technology that provides dire

144 Using fluorescence microscopy, fluorescence spectroscopy, and cell fraction

145 MOS) technology has greatly advanced optical microscopy for biomedical research with superior sensiti

146 us samples for single-particle electron cryo-microscopy for over three decades.

147 namely holotomography and transmission X-ray microscopy, for the quantitative 3D analysis of the evol

148 tion/desorption isotherms, scanning electron microscopy, Fourier-transform infrared spectroscopy, the

149 Single-molecule super-resolution microscopy has developed from a specialized technique in

150 Super-resolution fluorescence microscopy has enabled important breakthroughs in biolog

151 Here we used high-speed atomic force microscopy (HS-AFM) and kinetic modeling which allowed u

152 ts usefulness by studying scanning tunneling microscopy images of a Co-doped iron arsenide supercondu

153 d surface roughness obtained by atomic force microscopy images.

154 Here, we employed atomic force microscopy imaging in air and liquids to visualize ring

155 tion is intrinsically coupled to position in microscopy imaging, and molecular wobbling during the im

156 rm optical mapping and transmission electron microscopy in a drug-induced (sea anemone toxin, ATXII)

157 be combined with machine learning to enable microscopy in diverse fields from cancer diagnoses to fo

158 esolution imaging techniques, and two-photon microscopy in living knock-ins enables the visualization

159 recordings and molecular biology to confocal microscopy in primary cortical cultures, and from acute

160 orbance, circular dichroism and fluorescence microscopy indicated that the microfluidic control of th

161 Despite advances in diagnosis, smear microscopy insufficiently detects pulmonary disease, wit

162 Single-molecule localization microscopy is a powerful tool for visualizing subcellula

163 Intravital microscopy is increasingly used to capture the dynamics

164 nd, one of the primary tools in fluorescence microscopy is that of computational deconvolution.

165 Furthermore, Lorentz transmission electron microscopy is used to directly image Neel-type skyrmion

166 Widefield fluorescence microscopy is used to monitor the spiking of populations

167 ions of serial-section transmission electron microscopy, it was possible to reveal that the sub-retin

168 st of murine neutrophils in vitro Intravital microscopy (IVM) showed increased association of Ab-opso

169 However, TIR infrared microscopy lacks high spatial resolution due to the opti

170 ingle-molecule tracking and super-resolution microscopy, light-induced subcellular localization, reac

171 are challenging to detect with fluorescence microscopy, making it difficult to determine whether act

172 containing vacuoles observed with electronic microscopy, may be a useful histologic marker for active

173 in situ environmental transmission electron microscopy measurements herein show that pit formation i

174 h a combination of scanning PTE and electron microscopy measurements of single-crystal and bicrystal

175 east partially, LP-EM has evolved into a new microscopy method with nanometer spatial resolution and

176 Various analytical techniques and microscopy methods were employed to examine the composit

177 n by X-ray crystallography and cryo-electron microscopy not only confirms that IrtAB has an ABC expor

178 cell patch-clamp and 2-photon laser scanning microscopy of basket cells (BCs), we found that classica

179 Optical and electron microscopy of HIPK4-null male germ cells reveals defects

180 Focused ion-beam scanning electron microscopy of infected cells validated numerous membrano

181 urements in Xenopus oocytes, and fluorescent microscopy of mammalian cells.

182 We correlate stimulated-emission-depletion microscopy of proteins and synchrotron X-ray fluorescenc

183 y and total internal reflection fluorescence microscopy on fixed specimens.

184 for regular and single-molecule localization microscopy on live-cell samples.

185 Spectrally resolved fluorescence microscopy on single block copolymerized organic heteros

186 Recent advances in scanning probe microscopy on surface enable not only direct observation

187 lecule images for 3-dimensional localization microscopy or single-molecule tracking.

188 he following: they are prone to human error (microscopy) or expensive and time-consuming (polymerase

189 rostructured catalysts according to electron microscopy outcomes.

190 er-resolution Photo-Activatable Localization Microscopy (PALM) mapping of the static positions of SBF

191 epletion (STED), photoactivated localization microscopy (PALM), stochastic optical reconstruction mic

192 tious mitral endocarditis, were diagnosed by microscopy, PCR-based detections and culture: we showed

193 tralization, we generated cryogenic electron microscopy reconstructions of Fab:CHIKV complexes at 4-

194 r, generating meaningful data using confocal microscopy requires careful planning and a thorough unde

195 The scanning electron microscopy results showed void spaces on the treated mel

196 py and energy-filtered transmission electron microscopy reveal the well-associated optical and electr

197 sis of particulates by transmission electron microscopy revealed 2-10 nm crystallites of fcc-UO(2) or

198 Atomic force microscopy revealed 40-300 nm diameter OMVs from control

199 Superresolution microscopy revealed a reduced interaction of CG with the

200 Immunofluorescence staining and confocal microscopy revealed alterations in the structure and com

201 Superresolution microscopy revealed in infected cells the vertical displ

202 Confocal microscopy revealed in situ that bacteria formed a dense

203 Atomic force microscopy revealed that MFS CMs are stiffer compared to

204 monoclonal antibody (mAb5) by cryo-electron microscopy, revealing the tertiary and quaternary struct

205 Negative-stain electron microscopy reveals that the complex can adopt a variety

206 In addition, magnetic force microscopy reveals the ability to tune DMI in a range th

207 Atomic force microscopy reveals the Y269 residue is required for prop

208 We used a combination of cryo-electron microscopy, ribosome profiling, and mRNA stability assay

209 SD95 and SAP102), and Spinning Disc confocal Microscopy (SDM), to estimate the number of fluorescent

210 The combined use of scanning electron microscopy (SEM) and confocal laser scanning microscopy

211 ion using a combination of scanning electron microscopy (SEM) techniques.

212 stem which, assembled with scanning electron microscopy (SEM), is the most popular tool used in nanot

213 ctron microscopy (TEM) and scanning electron microscopy (SEM).

214 tomic force microscopy and scanning electron microscopy show clusters and, occasionally, isolated ind

215 Intravital microscopy showed decrease in leukocyte adhesion and rol

216 However, electron microscopy showed heterogeneity in the particles and a t

217 lso, ultrastructural examination by electron microscopy showed no evidence of viral particles in the

218 Confocal microscopy showed that GluD1 is preferentially colocaliz

219 Time-lapse microscopy showed that HuR was required for the promotio

220 old electron microscopy and super-resolution microscopy showed that ITPR3 in CCA cells was also in re

221 Time-lapse 3D confocal microscopy showed that self-lysis occurs locally at even

222 Scanning ion conductance microscopy (SICM) has emerged as a versatile tool for st

223 state and high speed structured illumination microscopy (SIM) to generate continuous gigapixel panora

224 croscopy (STORM) and structured illumination microscopy (SIM), has enabled functional imaging of cell

225 re we show through a series of cryo-electron microscopy single particle reconstructions how the Strep

226 ogy, mammalian cell culture and fluorescence microscopy skills.

227 le restructuring of Pd deposited on Ag using microscopy, spectroscopy, and novel simulation methods.

228 py (PALM), stochastic optical reconstruction microscopy (STORM) and structured illumination microscop

229 leosome interaction to empower cryo-electron microscopy structure determination of the complex at 3.1

230 ased on a recently solved cryogenic-electron microscopy structure of an active alpha(2)beta(2) comple

231 Here we present a cryo-electron microscopy structure of beta-arrestin 1 (betaarr1) in co

232 t the first, to our knowledge, cryo-electron microscopy structure of the eukaryotic EMC.

233 we present the high-resolution cryo electron microscopy structure of the GFLV-Nb23 complex, which pro

234 led coil according to the cryogenic electron microscopy structure of TRPM8.

235 Three cryoelectron microscopy structures of Fab in complex with Ross River

236 Here we present two cryo-electron microscopy structures of human PAC in a high-pH resting

237 Here, we report the cryo-electron microscopy structures of murine SIgA and dIgA.

238 Cryo-electron microscopy structures of Saccharomyces cerevisiae Spf1 r

239 Recent crystallography and electron microscopy studies have refined our model of herpesvirus

240 Fluorescent microscopy studies revealed 9-dechlorochrysophaentins le

241 l and total internal reflection fluorescence microscopy suggested that Amot's role in actin organizat

242 pid interactions in vitro, alongside optical microscopy techniques aimed at directly visualizing phas

243 A variety of microscopy techniques are used by researchers in the lif

244 y diffraction (p-XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM).

245 Traction force microscopy (TFM) has been instrumental for studying such

246 find by electron and structured illumination microscopy that knockdown of the a3-subunit altered the

247 rther exploited for studying with intravital microscopy the extravasation of 0.58 kDa rhodamine and 1

248 mbrane fusion can be tracked by fluorescence microscopy, the 3D configuration of proteins and lipids

249 In concert with microscopy, the metabarcoding data indicated a die-off o

250 der X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, inductively coup

251 determination and correlative light/electron microscopy, thus expanding the scope of cryogenic cellul

252 lectric field gradient from a scanning probe microscopy tip.

253 capsid structure, determined by cryoelectron microscopy to 3- angstrom resolution, has a similar surf

254 ulations, we used long-term in vivo 2-photon microscopy to compare morphology and basic functional pa

255 We used two-photon microscopy to elucidate the spatial organization, motili

256 Here we used cryo-electron microscopy to elucidate the structure of an agonist-boun

257 e report the use of scanning ion conductance microscopy to measure the ion permeability of GO films a

258 interactions in vivo by combining two-photon microscopy to monitor astrocyte calcium and electrocorti

259 e using plus-end tip tracking and intravital microscopy to quantify MT dynamics in live xenograft tum

260 We employed fluorescence polarization microscopy to show that cadherin order is not required f

261 We further used 2-photon and intravital microscopy to study endothelial activation and leukocyte

262 uantitative, single-molecule superresolution microscopy to study TNFR1 assembly directly in native ce

263 uated using a holistic approach ranging from microscopy to transcriptomics.

264 luorescence resonance energy transfer (FRET) microscopy to uncover the molecular mechanism for how su

265 C in 20 mTorr O(2) is shown by atomic force microscopy to yield nearly pinhole-free film growth whil

266 LM, single-molecule orientation localization microscopy, to directly measure the orientation spectra

267 Advances in imaging methods such as electron microscopy, tomography, and other modalities are enablin

268 Ultrasound localization microscopy (ULM) permits the reconstruction of super-res

269 Live cell microscopy using chemical and genetic reporters revealed

270 port was observed by confocal laser scanning microscopy using green fluorescent protein (GFP).

271 munohistochemistry and transmission electron microscopy verified that PIM inhibitors promote mitochon

272 Intravital microscopy via cranial window and flow cytometry showed

273 new studies use a whole adult brain electron microscopy volume to reveal new long-range connectivity

274 Leveraging a whole-brain electron microscopy volume, we studied the adult Drosophila melan

275 were fluorescently labeled, and fluorescence microscopy was employed to assess their electrophoretic

276 In this work, X-ray fluorescence microscopy was used to measure diffusion constants of K(

277 In this study, coherent Raman scattering microscopy was used to probe de novo intracellular lipid

278 focal analysis of non-fixed pancreatic islet microscopy we demonstrated that ODND probes may be used

279 M supported by fluorescence lifetime imaging microscopy we identified higher order assemblies contain

280 ing super-resolution microscopy and electron microscopy we identified, in adult cardiac myocytes, a N

281 Using cryo-soft X-ray microscopy we imaged intracellular calcium-containing pa

282 ecule total internal reflection fluorescence microscopy we show that Wsp1 synergizes with Dip1 to co-

283 methionine at residue 848 and cryo-electron microscopy, we determined structures that capture RAG en

284 By following invasion using video microscopy, we find a strong link between RBC tension an

285 Using correlative light and electron microscopy, we further demonstrated that one of these me

286 gh spatial and temporal resolution live-cell microscopy, we identified a role for mitochondria-lysoso

287 Here, using scanning tunnelling microscopy, we identify a new topological kagome magnet,

288 ith Raman spectroscopy and scanning electron microscopy, we investigated 10 papyri fragments from J.-

289 LC3B immunoblots, and live-cell fluorescence microscopy, we report here that in the presence of rumin

290 sensing, X-ray scattering, and Atomic Force Microscopy, we show that mammalian pulmonary membranes s

291 nuclear magnetic resonance and cryo-electron microscopy, we show that thiol groups of cysteine residu

292 e approach, which we validated with confocal microscopy, we significantly expand the list of epigenet

293 imulated emission depletion super-resolution microscopy were performed in prkar1 knock-out mouse embr

294 Live-cell imaging and microscopy were used to determine the effect of PIM loss

295 isometric vacuolization observed with light microscopy, which correlates with double-membrane vesicl

296 with ACs were monitored with epifluorescence microscopy, which revealed a local leaflet expansion upo

297 Users familiar with cryo-electron microscopy who get basic training in dual-beam microscop

298 By combining electron microscopy with glutamate immunogold labeling, we identi

299 this setup for fluorescence lifetime imaging microscopy with phasor analysis (FLIM/Phasor) and invest

300 nthanide ion binding, and X-ray fluorescence microscopy (XFM).