ライフサイエンスコーパス: light microscopy

1 ed depletion of intracytoplasmic granules by light microscopy.

2 c field of a quadruple electrode array using light microscopy.

3 specific imaging capabilites of fluorescence light microscopy.

4 the current super-resolution by fluorescence light microscopy.

5 arasites and be of interest to many users of light microscopy.

6 a reference standard of positive culture or light microscopy.

7 displacement technique were evaluated using light microscopy.

8 erely restricted by the diffraction limit of light microscopy.

9 visualized in detail by taking advantage of light microscopy.

10 break the diffraction-limited resolution of light microscopy.

11 ba) but had negative results via culture and light microscopy.

12 for analyzing neuronal MT organization using light microscopy.

13 c membranoproliferative pattern of injury on light microscopy.

14 uding proteomics, ionomics, and fluorescence light microscopy.

15 icult to visualize using diffraction-limited light microscopy.

16 deal with practical challenges in biological light microscopy.

17 luorescent, severely limiting the utility of light microscopy.

18 ffraction-limited resolution of conventional light microscopy.

19 -throughput neuroanatomy in Drosophila using light microscopy.

20 bril-like structures like those observed via light microscopy.

21 20-60 mum in diameter and readily imaged by light microscopy.

22 and light "tiger tail" banding on polarized light microscopy.

23 e original authors undertaken an analysis by light microscopy.

24 from 18 RAs were histologically examined by light microscopy.

25 o changes to the meat matrix were evident by light microscopy.

26 e limited spatial resolution of conventional light microscopy.

27 bronectin-coated microslides, Liu stain, and light microscopy.

28 ls the cellular nanoarchitecture by standard light microscopy.

29 eosin, periodic acid-Schiff, Congo red, and light microscopy.

30 sualize synapses in identified neurons using light microscopy.

31 90 days, specimens (n = 6) were obtained for light microscopy.

32 e the MT-Augmin-gamma-TuRC-MT junction using light microscopy.

33 esolvable by traditional diffraction-limited light microscopy.

34 ffraction-limited resolution of conventional light microscopy.

35 ta and histopathologic specimens examined by light microscopy.

36 Only 50% of these cases could be detected by light microscopy.

37 icrospheres and could be easily monitored by light microscopy.

38 Cytologic analysis was performed using light microscopy.

39 mall to be properly resolved by conventional light microscopy.

40 nd (ii) compare these findings with standard light microscopy.

41 otion estimation of biological structures in light microscopy.

42 during implant placement and analyzed under light microscopy.

43 raphic reconstructions, directly by standard light microscopy.

44 or protein distributions using conventional light microscopy.

45 was analyzed by a new method using polarized light microscopy.

46 ing were quantified using special stains and light microscopy.

47 X-ray micro-computed tomography, and optical light microscopy.

48 ade possible in several cases by advances in light microscopy.

49 a new temporal dimension for wide-field low-light microscopy.

50 al to 15 eosinophils per high-power field on light microscopy.

51 d in vivo x-ray microcomputed tomography and light microscopy.

52 six mammals using stereology techniques and light microscopy.

53 used for localizing proteins of interest by light microscopy.

54 at or below the 250 nm diffraction limit of light microscopy.

55 r genetic or exogenous contrast labeling for light microscopy.

56 l and mesenchymal components identifiable by light microscopy.

57 ion was evaluated with scanning electron and light microscopies.

58 ely to the diffraction limit of conventional light microscopy (200-300 nm).

59 ontrol kidneys appeared relatively normal by light microscopy; 3 of 20 specimens showed focal injury

60 Using genome editing and advanced light microscopy, a recent study has offered new insight

61 s, and therefore that evaluation by means of light microscopy after hematoxylin and eosin staining mi

62 e examined for the presence of fibrin, using light microscopy after Maurits, Scarlet and Blue stainin

63 spray ionization (nanoDESI), interfaced with light microscopy allows for protein profiling directly o

64 Superresolution light microscopy allows the imaging of labeled supramole

65 e imaging system using conventional confocal light microscopy and a specialized analysis software to

66 in operando platform composed of dark-field light microscopy and a transparent electrochemical cell

67 f the 21st century has seen a renaissance in light microscopy and anatomical tract tracing that toget

68 tify single cells in the Drosophila calyx by light microscopy and compared these with cell shapes, sy

69 ystals using ultrafast two-dimensional white-light microscopy and discover a low-energy singlet state

70 ng new genetic tags developed for correlated light microscopy and electron microscopy (the tetracyste

71 vast majority of Drosophila neuroanatomical light microscopy and electron microscopy connectomic dat

72 Here, we used light microscopy and electron microscopy to examine Nest

73 By integrating same-kinetochore light microscopy and electron microscopy, we demonstrate

74 We used light microscopy and electron tomography to elucidate me

75 rens junction complex assembly in situ using light microscopy and Fluorescence Covariance Analysis.

76 Simultaneous acquisition of phase-contrast light microscopy and fluorescently labeled bacteria, mov

77 echnology, such as combining high resolution light microscopy and genetically encoded Ca(2+) reporter

78 nfluenza B virus infection were evaluated by light microscopy and immunohistochemical assays for infl

79 day 14, and enucleated eyes were analyzed by light microscopy and immunohistochemistry.

80 rce microscopy (AFM), and Ti dissolution via light microscopy and Inductively-coupled Mass Spectromet

81 ctroscopic techniques, scanning electron and light microscopy and infrared spectroscopy were used to

82 comedullary-junction tubules by conventional light microscopy and Kim-1 immunostains, respectively (P

83 Correlative light microscopy and liquid-phase scanning transmission

84 By light microscopy and live-cell imaging, we show that CD6

85 n distinct tissue regions identified by both light microscopy and MS imaging.

86 While our light microscopy and mutant studies show that microtubul

87 Subdiffraction-resolution light microscopy and negative-staining electron microsco

88 We used superresolution light microscopy and platinum replica transmission elect

89 he limitations of the official methods (i.e. light microscopy and Polymerase Chain Reaction) suggest

90 The current official methods, light microscopy and polymerase chain reaction, do not f

91 lasmodium parasitaemia was carried out using light microscopy and qPCR.

92 Light microscopy and scanning electron microscopy (SEM)

93 Morphological evaluation performed by both light microscopy and scanning electron microscopy showed

94 transformations provide correlation between light microscopy and scanning electron microscopy/FIB.

95 Here we combined light microscopy and serial-section electron tomography

96 Transmitted light microscopy and synchrotron X-ray fluorescence imag

97 tic because of the axial resolution limit of light microscopy and the difficulty in preserving and an

98 The microstructure was evaluated using light microscopy and the effect of anthocyanins on lipid

99 itions for Z-ring assembly with fluorescence light microscopy and then prepared specimens for negativ

100 inspection was first achieved with inverted light microscopy and then the DeadEnd(TM) Fluorometric T

101 Fluorescence microscopy, light microscopy and time domain nuclear magnetic resona

102 ans and should be useful for a wide range of light microscopy and tomography techniques applied to bi

103 Morphology was assessed by light microscopy and transmission electron microscopy (T

104 tion, the ciliary epithelium was analyzed by light microscopy and transmission electron microscopy (T

105 Autophagy was characterized using light microscopy and transmission electron microscopy fo

106 Immunostaining was quantified by light microscopy and with a computerized image analysis

107 xylem anatomy and function using fluorescent light microscopy and x-ray computed microtomography.

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

109 ue can be performed by scientists trained in light microscopy and yields results in <1 week.

110 as observed by scanning electron microscopy, light microscopy, and changes in carbohydrate compositio

111 sites months after the initial presentation, light microscopy, and comprehensive immunohistochemistry

112 We demonstrate, using OCT, light microscopy, and electroretinography, that two Sfxn

113 olution micro-computed tomography (microCT), light microscopy, and fluorescence microscopy to charact

114 onfocal elastography, quantitative polarized light microscopy, and Fourier-transform infrared imaging

115 divisions were examined using tract tracing, light microscopy, and immunoelectron microscopy at four

116 ical examination, corneal photography, IVCM, light microscopy, and immunohistochemistry.

117 oned at 3 to 4 mm intervals and evaluated by light microscopy, and morphometric analysis was performe

118 rinogen, x-ray crystallography, electron and light microscopy, and other biophysical approaches, has

119 um covering these areas by stereomicroscopy, light microscopy, and scanning electron microscopy (SEM)

120 We used microspectrophotometry, light microscopy, and scanning electron microscopy to ch

121 s in the corneal epithelium were detected by light microscopy, and the MUC5AC transcript was detected

122 used a combination of molecular techniques, light microscopy, and transmission electron microscopy t

123 nological developments of ophthalmoscopy and light microscopy, and with the introduction of surgical

124 To address this, we devise a light microscopy approach for connectivity analysis of d

125 ge, there are two more critical links in the light microscopy approach: labeling and quantitative ana

126 Light microscopy approaches aimed to indirectly determin

127 More sensitive techniques than light microscopy are available to analyze the presence o

128 Third, particles identified from light microscopy are compositionally mapped at high defi

129 fibrillar protein aggregates and visible by light microscopy, are responsible for cell death in thes

130 been constrained by the diffraction limit of light microscopy, as the cisternae are only 10-20 nm thi

131 at allow them to be readily distinguished by light microscopy, as well as distinct suites of proteins

132 yo-stage allowing for spinning-disk confocal light microscopy at cryogenic temperatures and describe

133 allowing nearly any protein to be imaged by light microscopy at submicrometer spatial resolution and

134 action limits the resolution of conventional light microscopy at the lateral focal plane to 0.61lambd

135 ue characterization by means of conventional light microscopy-based histology, immunohistochemistry,

136 ructure that is too small to be imaged using light microscopy), but the field of view is limited and

137 38 patients, crystals were not detectable by light microscopy, but they were visible by electron micr

138 M), a method for improving the resolution of light microscopy by physically expanding a specimen, has

139 otein) fusions and complementation-activated light microscopy (CALM) for subresolution imaging of ind

140 However, conventional light microscopy can only achieve a resolution of approx

141 s for detection and typing of HSV, including light microscopy, culture, serology, and nucleic acid-ba

142 Both electron microscopy and light microscopy data show that H129 capsids and envelop

143 tailored to the specific characteristics of light microscopy datasets: super-voxels help registratio

144 ility, textural and sensory properties using light microscopy, differential scanning calorimetry (DSC

145 advances in high-throughput cell analysis by light microscopy, electron microscopy, and flow cytometr

146 with other microscopy techniques, including light microscopy, electron microscopy, cryomicroscopy, a

147 Using quantitative light microscopy, electron tomography, laser-mediated ab

148 Light microscopy established that the random network arc

149 were procured after death and processed for light microscopy evaluation.

150 ew important aspects of designing a rigorous light microscopy experiment: validation of methods used

151 Polarized light microscopy experiments not only proved the SCSC na

152 ough a combination of surface patterning and light microscopy experiments we show that vinculin can b

153 We reviewed light microscopy findings in all autopsies and performed

154 oral information from live-cell fluorescence light microscopy (fLM) to high-resolution cellular ultra

155 spatiotemporal information from fluorescence light microscopy (fLM) with high-resolution structural d

156 Using fluorescence light microscopy (fLM), direct stochastic optical recons

157 copic data of various modalities and scales (light microscopy, fluorescence microscopy, electron micr

158 on of the PNA microcapsules were analysed by light microscopy, fluorescent microscopy, scanning elect

159 d discusses several of the major advances in light microscopy for imaging cleared tissue.

160 andard cytochemical biomarkers and polarized light microscopy for microplastic tracking in tissue.

161 Here, we combine the efficiency of light microscopy for revealing cellular functions using

162 describe here a strategy based on polarized light microscopy for the quick and accurate measurement

163 NTB phase has been confirmed using polarized light microscopy, freeze fracture transmission electron

164 Samples were imaged using visible light microscopy fresh, 1-minute and 24-hours post-fixat

165 By light microscopy, GPER1-immunoreactivity (IR) was most n

166 Light microscopy has historically been a central method

167 Light microscopy has long been an indispensable tool for

168 Light microscopy has several features that make it ideal

169 tubules mistaken for sheets by conventional light microscopy, highlighting the importance of revisit

170 Conventional and super-resolution light microscopy identified significantly elevated frequ

171 Routine light microscopy identifies two distinct epithelial cell

172 Compared with Congo-red-based light microscopy, IEM was equally sensitive (75% to 80%)

173 that could be applied to any two-dimensional light microscopy image of stained nuclei across experime

174 Direct volume rendering of serial 6.25 x light microscopy images did not demonstrate the major ch

175 We also applied it to light microscopy images of cytoskeletal and nucleoskelet

176 ghted the advantages of 3D reconstruction of light microscopy images.

177 ative PCR (qRT-PCR) confirmed the results of light microscopy immunochemical analysis.

178 nce and structural organization over time by light microscopy, immunocytochemistry, metabolic imaging

179 Guidelines for the report format, light microscopy, immunofluorescence microscopy, electro

180 tion following renal injury as determined by light microscopy, immunohistochemistry, and intrarenal m

181 Histopathological examination included light microscopy, immunohistochemistry, and morphometry.

182 Tissue examination was done by light microscopy, immunohistochemistry, electron microsc

183 s were preserved in fixative and analyzed by light microscopy/immunostaining or electron microscopy f

184 n all cases, no organisms were identified by light microscopy in any of the 7 specimens.

185 Here I provide a brief introduction to using light microscopy in cell biology, with particular emphas

186 tion there (visualized by silver enhancement light microscopy in combination with transmission electr

187 Light microscopy in one patient demonstrated scarring li

188 Polarized light microscopy in Sirius red-stained sections demonstr

189 The core samples were evaluated by routine light microscopy, including immunohistochemical/immunofl

190 Polarized light microscopy indicated alterations in collagen fiber

191 The examination of tissue histology by light microscopy is a fundamental tool for investigating

192 Light microscopy is a key tool in modern cell biology.

193 Light microscopy is a powerful tool for probing the conf

194 Multi-label electron or confocal light microscopy is required to examine specific types o

195 generally close to the diffraction limit of light microscopy, it is often challenging, if not imposs

196 ral resolution exceeding diffraction-limited light microscopy, lack of contrast has largely limited u

197 -moving cells on flat surfaces, conventional light microscopy lacks the spatial and temporal resoluti

198 o unique and extremely beneficial aspects of light microscopy: live-cell imaging in multiple colors.

199 o separate microscope platforms: fluorescent light microscopy (LM) and electron microscopy (EM).

200 s over large volumes remains challenging for light microscopy (LM) and electron microscopy (EM).

201 ermeabilization, thereby enabling correlated light microscopy (LM) and EM studies.

202 eri-implantitis biopsies were analyzed using light microscopy (LM) and scanning electron microscopy (

203 Using both light microscopy (LM) and transmission electron microsco

204 We conducted super-resolution light microscopy (LM) imaging of the distribution of rya

205 y culture or fungal structures identified by light microscopy (LM) of scrape material, histopathology

206 Iridocorneal angles were examined using light microscopy (LM), immunofluorescence (IF), and tran

207 uits, including electron microscopy (EM) and light microscopy (LM).

208 because the nucleolinus is easily visible by light microscopy, making it accessible by laser microsur

209 large carotenoid crystals clearly visible by light microscopy, mango and papaya contained different t

210 stimates based on thermokinetic modeling and light microscopy measurements.

211 e processing including: electron microscopy, light microscopy, medical X-ray imaging, astronomy, etc.

212 hotography, subjective clinical improvement, light microscopy, melanin index, reflectance spectroscop

213 We developed a high-throughput light microscopy method, validated by electron microscop

214 Low-light microscopy methods are receiving increased attenti

215 o enable clearing and 3D tissue imaging with light microscopy methods, we developed a colorimetric, n

216 rther study from bright-field and dark-field light-microscopy modes, respectively.

217 recent development of super-resolution (SR) light microscopy now allows the visualisation of viral s

218 erent neoplasms, and for correlation between light microscopy observations and computerized image ana

219 standard for malaria detection remains basic light microscopy of Giemsa-stained patient blood smears

220 Light microscopy of immunostained TbHrg indicated locali

221 tion, enzyme assays, chlorophyll content and light microscopy of leaves were used to characterize acc

222 Super-resolution light microscopy of mutants, cryo-electron tomography, b

223 Light microscopy of proximal tubules showed geographic i

224 Manual light microscopy of stool remains the gold standard but

225 transport in combination with the polarized light microscopy of structural domains in mesoscopic LAO

226 Preceding light microscopy of the living cells allowed correlating

227 splant glomerulopathy (Banff cg score >=1 by light microscopy), on the basis of biopsies performed fr

228 the biopsy yielded at least 10 glomeruli at light microscopy, one glomerulus at immunofluorescence m

229 s advice on how to identify microcrystals by light microscopy or by negative-stain electron microscop

230 chinery-intensive process, relying on either light microscopy or direct physical registration.

231 y and--being designed almost exclusively for light microscopy or electrophysiology studies--seldom in

232 variable expanses of empty tubule as seen by light microscopy or EM.

233 ions: either histological sections imaged by light microscopy, or electron micrographs of single ultr

234 examination of two smears with Ziehl-Neelsen light microscopy over 2 days, examination of two smears

235 By light microscopy, pDOR-immunoreactivity (ir) was located

236 Recent advances in light microscopy permit visualization of the behavior of

237 to conduct a clinicopathologic and polarized light microscopy (PLM) analysis of 14 new I-RLs and comp

238 ensile stress-strain curves and polarization light microscopy (PLM) of the polymer electrolyte film r

239 laria in pregnancy was not confirmed by PCR, light microscopy, rapid diagnostic test, or histology.

240 In light microscopy, refractive index mismatches between me

241 ria is endemic and are often undetectable by light microscopy, rendering their study in human populat

242 ochemistry by autofluorescence and polarized light microscopy, respectively.

243 rganisms in deep ulcers in which culture and light microscopy results were negative.

244 Live-imaging approaches based on light microscopy reveal the intricate dynamics of this p

245 Quantitative light microscopy revealed a significant increase in pDOR

246 Light microscopy revealed clear healing of the corneal e

247 Polarized light microscopy revealed large amounts of birefringent

248 ng produced micropores in the cell walls and light microscopy revealed that NaOH steeping increased d

249 Time-lapse fluorescence light microscopy reveals that sheaths of the type VI sec

250 al, several analytical techniques (reflected light microscopy, scanning electron microscopy with ener

251 136 nonatherosclerotic swine and examined by light microscopy, scanning electron microscopy, pharmaco

252 Light microscopy showed loss of normal stromal collagen

253 calized with virus budding structures, while light microscopy showed that they excluded a freely diff

254 o performed using bright-field and polarised light microscopy, small-angle and wide-angle X-ray scatt

255 Dermal-epidermal separation was assessed by light microscopy studies and quantified using Fiji softw

256 d around the cartwheel, and super-resolution light microscopy studies have measured the average radii

257 Light microscopy studies showed marked edema of the papi

258 Research modalities include various light microscopy techniques (confocal, multiphoton, tota

259 on Mass Spectrometry (NanoSIMS) approach and light microscopy techniques to follow formation of NR by

260 reflection (DFSR) are advanced but expensive light microscopy techniques with limited availability.

261 able, we provide guidance for using standard light microscopy techniques, as well as recommending sta

262 nctional analysis with standard and advanced light microscopy techniques.

263 Here, we show by quantitative light microscopy that the protein abundance of NHE6 is d

264 Using light microscopy, the anterior half of the stroma displa

265 In the field of light microscopy, the Bio-Formats library was designed t

266 In three-dimensional light microscopy, the heterogeneity of the optical densi

267 In addition to light microscopy, the majority of the biopsies were asse

268 e has drastically improved the resolution of light microscopy to approximately 10 nm, thus creating e

269 R absorption, fluorescence spectroscopy, and light microscopy to characterize the mesoscopic phase st

270 d serial block-face electron microscopy with light microscopy to determine the cell types targeted by

271 , 1758) and dissected the ventral tube using light microscopy to elucidate the fine structure and the

272 cused ion beam (FIB) milling and correlative light microscopy to ensure that the event of interest is

273 erformed using polarization filter reflected light microscopy to identify CC.

274 l electron microscopy, electrophysiology and light microscopy to illustrate the wiring patterns in mo

275 ns were studied by confocal and conventional light microscopy to quantify hair cells, cochlear neuron

276 th energy-dispersive x-ray spectroscopy, and light microscopy to quantify, localize, and assess the e

277 P-MS), transmission electron microscopy, and light microscopy to quantify, localize, and assess the e

278 e opsin expression in B. mysticetus, whereas light microscopy, transmission electron microscopy, and

279 Electroretinography (ERG), histology, light microscopy, transmission electron microscopy, and

280 A combination of light microscopy, transmission electron microscopy, RNA-

281 Autopsy tissue samples were evaluated by light microscopy, Warthin-Starry stain, immunohistochemi

282 the number of fractures per scaffold seen on light microscopy was 6.0 (5.0-10.5) when overexpanded 1.

283 ickness were measured for all specimens, and light microscopy was performed for those surviving surge

284 Light microscopy was used to evaluate specimens for infl

285 Polarized light microscopy was used to localize crystallinity indu

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

287 co-inspiration with India ink and polarized light microscopy, was highly dependent upon volume.

288 ching reconstructed neurons to examples from light microscopy, we assigned neurons to cell types and

289 cales near or below the diffraction limit of light microscopy, we developed a superresolution imaging

290 h cells are easy to identify and quantify by light microscopy, we evaluated the mean number of Paneth

291 cerevisiae Using cell-free fusion assays and light microscopy, we find that GTPase activation and tra

292 tag for electron microscopy and ratiometric light microscopy, we go on to show that bulk membrane pr

293 E. coli filamentation was observed by light microscopy when cells were grown in the presence o

294 ubular isometric vacuolization observed with light microscopy, which correlates with double-membrane

295 t adequately resolved by diffraction-limited light microscopy, which has limited our understanding of

296 The approach was designed for light microscopy, which is compatible with the mild fixa

297 tion is below the resolution of conventional light microscopy, which makes analysis of these interact

298 Comparison of our results from light microscopy with a mathematical model suggests that

299 Here, we combine photoactivated light microscopy with quantitative statistical analysis

300 ividual virus-associated objects observed in light microscopy with ultrastructural features seen by e