ライフサイエンスコーパス: tissue section

1 f other biological specimens (e.g., clinical tissue sections).

2 analysis of sub regions of a rat cerebellum tissue section.

3 s the local concentration of RIF in the thin tissue section.

4 proteins from spatially defined regions of a tissue section.

5 ggests the presence of GdPO4 deposits in the tissue section.

6 es in seven different regions of a rat brain tissue section.

7 toxylin and eosin (H&E) staining on the same tissue section.

8 tical approaches in the analysis of a single tissue section.

9 proteins from spatially distinct areas of a tissue section.

10 e Opal 7 color Kit (PerkinElmer) in the same tissue section.

11 ution of molecules at a high resolution on a tissue section.

12 inding and tau antibody staining on the same tissue section.

13 p the 3D fibre orientation across the entire tissue section.

14 nked glycans and proteins from the same FFPE tissue section.

15 different proteins transferred from a single tissue section.

16 ng activity in fixed paraffin-embedded (FPE) tissue sections.

17 s and formalin-fixed paraffin-embedded human tissue sections.

18 ribution images of an analyte or analytes in tissue sections.

19 rom formalin-fixed, paraffin-embedded (FFPE) tissue sections.

20 ify automatically tumor viability on unknown tissue sections.

21 f myocardial caspase 3 and TUNEL staining of tissue sections.

22 bundant analyte identification directly from tissue sections.

23 tissue observations and histomorphometry of tissue sections.

24 rence to visualize the lipid distribution in tissue sections.

25 trace amounts of cocaine in mouse brain thin tissue sections.

26 to profile discrete spots on the surface of tissue sections.

27 s and is applicable for detection in primary tissue sections.

28 ecular lipid species extracted directly from tissue sections.

29 for lipid distributions in mouse brain thin tissue sections.

30 dissected, formalin-fixed, paraffin-embedded tissue sections.

31 toradiographic images obtained from adjacent tissue sections.

32 uantification of phospholipids in thin brain tissue sections.

33 edding media greatly improved the quality of tissue sections.

34 PV type was observed in 15 (48%) of 31 whole-tissue sections.

35 atic removal of candidate carbohydrates from tissue sections.

36 DI-MSI) to profile lipids in D. melanogaster tissue sections.

37 ant staining of 5LO was detected in human KS tissue sections.

38 on 100-microm cerebellar cortical vibratome tissue sections.

39 fication of analyte molecules extracted from tissue sections.

40 uorophore, are hybridized to target mRNAs in tissue sections.

41 unt of information that can be obtained from tissue sections.

42 using immunohistochemical techniques in lung tissue sections.

43 (Persea americana) mesocarp and mouse brain tissue sections.

44 n colorectal cancer liver metastasis (CRCLM) tissue sections.

45 collection of specific cell populations from tissue sections.

46 d in situ characterization of lipids in thin tissue sections.

47 ith decreased numbers of osteoclasts in bone tissue sections.

48 ng, lymph node, trachea, and nasal turbinate tissue sections.

49 through registration and stacking of serial tissue sections.

50 pically complex cell populations directly in tissue sections.

51 system is demonstrated by imaging rat brain tissue sections.

52 unmasked and imaged directly from biological tissue sections.

53 chemical mapping of lipids at the surface of tissue sections.

54 ed probes for imaging enzyme active sites in tissue sections.

55 rescence and immunohistochemical analysis of tissue sections.

56 apping of various analytes within biological tissue sections.

57 nt in situ hybridization analyses of gastric tissue sections.

58 ging of relatively flat samples such as thin tissue sections.

59 n and quantification of drugs in animal thin tissue sections.

60 oncomitant Abeta plaques in human AD Braak V tissue sections.

61 with immunostaining of human and mouse HNSCC tissue sections.

62 or detecting amyloid fibrils in solution and tissue sections.

63 rnative to MALDI MS for imaging of TAGs from tissue sections.

64 ) elucidates molecular distributions in thin tissue sections.

65 ts of ECM are usually performed on cryotomed tissue sections.

66 lar spatial resolution in vivo or in situ in tissue sections.

67 emical detection of glycogen on the adjacent tissue sections.

68 tween surrogate tissue sections and incurred tissue sections.

69 e potential molecular targets in human tumor tissue sections.

70 glycogen and lactate, in situ within ex vivo tissue sections.

71 nd mass spectrometry from fixed histological tissue sections.

72 olor reproduction of DCFM by imaging stained tissue sections.

73 ulfonate group in taurine in situ in ex vivo tissue sections.

74 and the number of SIV RNA-positive cells in tissue sections.

75 r-quantitatively degrade PCs in fresh-frozen tissue sections.

76 e and when applied to fixed human colorectal tissue sections.

77 r global proteomics analysis from ten 10 mum tissue sections.

78 tissue layers, thus eliminating the need for tissue sectioning.

79 ins by integrating two-photon microscopy and tissue sectioning.

80 In an additional 14 whole-tissue sections, 1 HPV type was found in each lesion sam

81 with sequential removal of ultrathin surface tissue sections achieved either by ablation with a focus

82 LDI imaging mass spectrometry of lipids from tissue section after deposition by sublimation.

83 MS ion images of planarian tissue sections allow changes in peptides and unknown co

84 ements on acutely isolated mouse spinal cord tissue sectioned along the three major anatomical planes

85 tection of low-molecular weight compounds in tissue sections, analyzed by matrix assisted laser desor

86 yloid structures can coexist within a single tissue section and (iii) within individual plaques there

87 inol as matrix for spray deposition onto the tissue section and implementation of "soft" acquisition

88 filing to allow multiple targets in the same tissue section and we provide that is accurate and repro

89 dependent verification using standard serial tissue sectioning and quantification methods.

90 ates the identification workflow by avoiding tissue sectioning and slide preparation.

91 Histopathology based on tissue sectioning and staining has been the gold standar

92 bit monoclonal antibodies, in 49 NSCLC whole-tissue sections and a corresponding tissue microarray wi

93 nt surveillant or activated microglia within tissue sections and by flow cytometric analyses.

94 f antibodies, raised in the same species, in tissue sections and cultured cells.

95 rains, imaged haloperidol abundance in brain tissue sections and directly measured haloperidol (and i

96 yses of viral nucleoprotein staining of lung tissue sections and dissociated lung cells.

97 pectrometry has previously been reported for tissue sections and dried blood spot samples.

98 antitatively identifies particles in ex vivo tissue sections and enables detailed observations of acc

99 diography studies of [(18)F]-9 with AD brain tissue sections and ex vivo autoradiography studies in t

100 Small airways were identified on serial tissue sections and examined for epithelial morphology,

101 is of the TGFbeta and VEGF signaling axes in tissue sections and explanted smooth muscle cells.

102 values for D were directly measured in thick tissue sections and in 3- to 5-mum sections using calibr

103 yl peptidyl receptor (ALX/FPR) in KS patient tissue sections and in vitro KS and PEL cell models offe

104 on efficiency was observed between surrogate tissue sections and incurred tissue sections.

105 on, we detected OBSL1 expression in cervical tissue sections and noted the involvement of OBSL1 durin

106 ied as a method to localize analytes on thin tissue sections and other surfaces.

107 o) statistical method to diagnose pancreatic tissue sections and prospectively evaluate surgical rese

108 spectrometry (MALDI-IMS) on flat-mounted RPE tissue sections and retinal cross-sections.

109 results open the door for matrix-free MSI of tissue sections and small cell populations by nanophoton

110 d by the direct LAAPPI analysis of rat brain tissue sections and sour orange (Citrus aurantium) leave

111 Tissue sections and spotted samples first undergo on-sur

112 muscle cell (SMC) lineage in human and mouse tissue sections and that the mark persists even in pheno

113 Electron microcopy of lung tissue sections and tissue subcellular fractionation bot

114 We apply muMAPPS to fixed tissue sections and to the study of the collagen microsc

115 l of neuronal arrangements derived from thin tissue sections and validated in brain tissue from rhesu

116 FISSEQ is compatible with tissue sections and whole-mount embryos and reduces the

117 smFISH has been developed for culture cells, tissue sections and whole-mount invertebrate organisms,

118 primarily been studied by staining of fixed tissue sections, and a clear understanding of the behavi

119 tial distribution of glycans associated with tissue sections, and may be correlated with immunofloure

120 nd sulfatides) were scrutinized on rat brain tissue sections, and systematic MS/MS studies were condu

121 After clearing, plant organs and thick tissue sections are amenable to deep imaging.

122 ith immunoflourescence imaging when adjacent tissue sections are analyzed.

123 In this method, fresh-frozen tissue sections are fixed, incubated with the probe and

124 f HER2 expression and heterogeneity within a tissue section at the single-cell level.

125 tected and imaged in 20 mum-thick whole-body tissue sections at a spatial resolution of 12 mum per im

126 ndomicroscopic SHG images of murine cervical tissue sections at different stages of normal pregnancy

127 e different lipid species were obtained from tissue sections at high spatial resolution and the detec

128 a-glycerylphosphorylcholine, in histological tissue sections at high spatial resolutions.

129 tend this work, we examined small-intestinal tissue sections at various time points after ST infectio

130 gional I2BS densities as determined by human tissue section autoradiography and preclinical in vivo P

131 tor densities and distribution determined by tissue-section autoradiography in preclinical species an

132 tion in formaldehyde-fixed paraffin-embedded tissue sections based on combined use of in situ hybridi

133 architecture mapping (nanoNAM) of unstained tissue sections based on the intrinsic density alteratio

134 the context of single cells, laser tweezers, tissue sections, biopsies and whole animals.

135 teins, peptides and metabolites in different tissue sections, but its application to environmental re

136 h the activity of the mAbs in binding to CNS tissue sections, but not with other in vitro assays.

137 l distribution of different lipid classes in tissue sections, but the applicability of the method to

138 rnea have been restricted to examinations of tissue sections by conventional light or electron micros

139 d ex vivo and in vivo and analysis of frozen tissue sections by immunofluorescence microscopy showed

140 Gene repositioning is analyzed in patient tissue sections by labeling sequences with fluorescence

141 the analysis of triacylglycerols (TAGs) from tissue sections by laser desorption ionization (LDI) ima

142 ved quantitation of chemical species in thin tissue sections by mass spectrometric methods has been c

143 spatial mapping of drugs and metabolites in tissue sections by nano-DESI imaging.

144 Regions-of-interest in a tissue section can be analyzed based on a number of quan

145 but not CXCL1 was significantly increased in tissue sections close to the interdental region, consist

146 Histological examinations of tissue sections confirm the ability of the NR system to

147 etection of pimonidazole adducts on adjacent tissue sections confirmed that this metabolite is locali

148 Two whole-tissue sections contained collision regions, each with 2

149 Further analysis of testis and epididymis tissue sections demonstrated that only epithelial cells

150 r (TfR) colocalization in ex vivo intestinal tissue sections, despite blocking of the receptor with t

151 enzyme-laced hydrogel discs are applied to a tissue section, directing enzymatic digestion to a spati

152 own to give the same chemical information as tissue sections, eliminating the need for sectioning bef

153 ification of the expression of biomarkers on tissue sections, enabled by the ultra-rapid and uniform

154 d intima-related regions of rabbit and human tissue sections ex vivo.

155 stimating a fast initial alignment using the tissue sections' external boundaries, followed by an eff

156 an alkyne group to serine hydrolases in the tissue section followed by attachment of the dendrimer l

157 ng the distribution of nicotine in rat brain tissue sections following in vivo drug administration.

158 aking it ideal for rapid sampling of thicker tissue sections for electrophysiological and other neuro

159 the utility of metallic silver sputtering on tissue sections for high resolution imaging mass spectro

160 A 40-mum FFPE tissue section from each specimen was digested with prot

161 PFC tissue sections from 20 matched pairs of schizophrenia a

162 Prefrontal cortex tissue sections from 20 matched pairs of schizophrenia a

163 Experiments were performed on tissue sections from 20 patients undergoing surgery for

164 traoperative use by analyzing and diagnosing tissue sections from 32 surgical specimens obtained from

165 t microscopic images with MSI images of thin tissue sections from a breast tumor model.

166 Similar defects are evident in tissue sections from AKAP220-KO mice.

167 affinity and restored anti-VCAM-1 binding in tissue sections from ApoE(-)/(-) mice ex vivo.

168 for creating standard curves using surrogate tissue sections from blank tissue homogenate spiked with

169 stochemistry for HER2 was performed on whole-tissue sections from each tumor.

170 ast cancer cells in culture and in malignant tissue sections from ER+ breast tumors, HDAC6 localizes

171 Electron tomography on tissue sections from fixed and stained axon terminals of

172 cores of beta-amyloid plaques in postmortem tissue sections from frontal, temporal, and occipital ne

173 was downregulated by HBx in HepG2X cells and tissue sections from HBV-infected patients.

174 unohistochemical staining of liver and tumor tissue sections from HBV-infected patients.

175 4v6 and Met colocalize in fibroblasts and in tissue sections from ILD patients and in lungs of bleomy

176 hese studies are that they were performed on tissue sections from immunocompromised or germ-free host

177 Paraffin-embedded tissue sections from normal human skin and hyperprolifer

178 e analyzed by immunostaining first in single tissue sections from normal stomach, metaplasia, and gas

179 s II-restricted antigen in paraffin-embedded tissue sections from patients with brain tumors.

180 Human ocular tissue sections from patients with geographic atrophy or

181 Immunohistochemistry was performed on lung tissue sections from patients with idiopathic PAH and he

182 Using tissue sections from patients with malignant melanoma, i

183 In tissue sections from patients with primary amyloidosis,

184 ificantly up regulated in inflammatory colon tissue sections from patients with ulcerative colitis (p

185 epatic FGF21 activation in liver tissues and tissue sections from several mouse liver disease models

186 f regenerating nerve axons, was performed on tissue sections from the R1 lobe of the regenerating liv

187 Tissue sections from the root associated mesial (anterio

188 Primary distal PAVSMCs, lung tissue sections from unused donor (control) and idiopath

189 We found that articular cartilage tissue sections from y/y mice of up to 6 months of age c

190 s spectrometry (IMS) of muscle and abdominal tissue sections identified the drug content primarily wi

191 Many current techniques for tissue sectioning, imaging and analysis are time-consumi

192 of multiparametric information by creating a tissue section imprint on an SPRi sensor surface.

193 issection of nuclei across an FFPE rat brain tissue section in milliseconds.

194 isolated microfibrils and to microfibrils in tissue sections in a dose-dependent manner.

195 Our unsupervised method for thin lung tissue sections in murine fungal pneumonia achieved sens

196 This approach can be extended to whole tissue sections in order to generate images of the secti

197 s spectrometry imaging of proteins from thin tissue sections in raster mode and discuss advantages (a

198 Washing the tissue sections in the buffered solution resulted in rem

199 dentification of lipid species desorbed from tissue sections in the negative mode can be significantl

200 normal colon tissue whereas the majority of tissue sections in ulcerative colitis and Crohn's diseas

201 more, evaluation of Vdr(-/-) BDL mouse liver tissue sections indicated altered E-cadherin staining as

202 ons of MALDI coupled with the homogeneity of tissue sections inherent in an MSI experiment.

203 The histology tissue section is annotated and then automatically regis

204 The tissue section is stamped onto a fluorocarbon-functional

205 Finally, a freshly thawed retina tissue section is used to demonstrate the success of dec

206 h tissue section the histology from adjacent tissue sections is used to focus the analysis on the are

207 Immunohistochemistry (IHC) on tissue sections is widely used for quantifying the expre

208 Careful scrutiny of tissue sections led to detection of the presence of micr

209 biological samples (e.g., fixed cytology and tissue sections, live cells or biofluids) that assesses

210 ral circuit, typically employ thick, ex vivo tissue sections maintained under near-physiological cond

211 w strategy, involving the microdissection of tissue sections mounted on parafilm M-covered glass slid

212 top-down protein analysis directly from thin tissue sections (mouse liver, mouse brain) and from bact

213 ister images from different modalities, each tissue section must contain points of reference, which a

214 ssment of hematoxylin and eosin stained thin tissue sections obtained from the Raman measurement loca

215 DNA was isolated from whole-tissue sections of 31 high-grade AIN that were recovered

216 Binding of tritiated compounds to brain tissue sections of AD patients and healthy controls was

217 tative autoradiography studies on postmortem tissue sections of human Alzheimer's disease brains show

218 actin or collagen 1alpha in left ventricular tissue sections of IL10KO chimeric mice suggests that my

219 Microscopic tissue sections of interest were taken on PALM slides an

220 nolol in mouse brain, kidney, and liver thin tissue sections of mice administered with the drug at a

221 in complex can be sampled directly from thin tissue sections of mouse liver and correlated to a visib

222 t tissue homogenate not detectable in frozen tissue sections of myocardial biopsy of affected males.

223 We examined lung tissue sections of persons with chronic obstructive pulm

224 gative ion detection of endogenous lipids on tissue sections of porcine adrenal glands by MALDI-Fouri

225 Applied to tissue sections of rat pituitary, the platform demonstra

226 or metabolite 2-hydroxyglutarate (2-HG) from tissue sections of surgically resected gliomas, under am

227 microdissection to isolate the decidua from tissue sections of the maternal-fetal interface in sPE.

228 dA-AL-I was then measured in 10-mum thick tissue-sections of FFPE kidney from patients with upper

229 ) direct labelling of DSBs in fixed cells or tissue sections on a solid surface; (2) low-input requir

230 to quantify sub-micron features within large tissue sections.Optical clearing of tissue has enabled o

231 HSCs are rare and few can be found in thin tissue sections or upon live imaging, making it difficul

232 method is suitable for preparation of single tissue sections, or as an immersion fixation method for

233 arious materials including urine, biological tissue sections, paper, and plant material on a low pump

234 We used tissue sections, plasma, and lung fibroblasts from patie

235 mmunohistochemistry, iron was detected in MS tissue sections predominantly in non-phagocytosing macro

236 oleucine(8) Ang II) in brain homogenates and tissue sections prepared from rats given repeated inject

237 Thin tissue sections (rat kidney and mouse or rat brains) wer

238 he standard and subsequently the matrix onto tissue sections resulted in quantitation that was not st

239 tu lipidomic and proteomic analyses on brain tissue sections revealed distinct, brain region-specific

240 mmunogold electron microscopy of hippocampal tissue sections revealed extensive localization of NR2a

241 mage was acquired over a small region of the tissue section revealing the distribution of an abundant

242 on of calibration curves to quantify unknown tissue section samples.

243 ing and quantitative image analysis of whole tissue sections showed a significant increase of EZH2 ex

244 Immunohistochemistry on mouse tissue sections showed intense Na(V)1.8 labeling in dors

245 sed formalin-fixed, paraffin-embedded (FFPE) tissue section soaked in a polyethylene glycol solution.

246 ded visual signs of tissue damage in cardiac tissue sections stained with hematoxylin and eosin.

247 -fixed, paraffin-embedded human breast tumor tissue sections stained with ten labels simultaneously.

248 polyclonal antibodies were performed on all tissue sections that contained inflammation.

249 SI; instead of analyzing large parts of each tissue section the histology from adjacent tissue sectio

250 For mouse brain tissue section, the thickness was adjusted to 23 +/- 2 n

251 In mouse brain and kidney tissue sections, the distributions of over 80 putatively

252 automatically registered to the MSI-prepared tissue section; the registration transformation is then

253 by the equation CF=1/(D/T+1), where T is the tissue section thickness and D is the mean caliper diame

254 Regularly spaced tissue sections through the entire extent of the nasal c

255 -tissue MS/MS was also performed on the same tissue section to identify lipid ions that showed spatia

256 er proteins was performed on a breast cancer tissue section to illustrate the potential of this metho

257 ing points at 1 mm spatial resolution across tissue sections to build an image of xenobiotic and endo

258 ly labeled internal standards are applied to tissue sections to maximize quantitative reproducibility

259 ed in formalin-fixed paraffin embedded brain tissue sections, uncovering correlated increase in abund

260 rared laser was used to ablate material from tissue sections under ambient conditions for direct coll

261 ne and two of its metabolites spotted onto a tissue section using deuterated internal standard.

262 tau aggregates and Abeta plaques on the same tissue section using specific antibodies.

263 Subsequent analysis of adjacent tissue sections using DESI-MSI is also reported.

264 Examination of tissue sections using desorption electrospray ionization

265 sue on formalin-fixed, paraffin-embedded HCA tissue sections using laser capture methodology, we perf

266 dividual cell populations isolated from FFPE tissue sections using laser capture microdissection.

267 el method for the quantification of drugs in tissue sections using matrix-assisted laser desorption/i

268 Overlay analyses of dermal tissue sections using the recombinant versican G1 domain

269 being detected in rat liver and bovine lens tissue sections, using positive-ion detection.

270 an be visualized within individual cells and tissue sections via fluorescence microscopy is limited b

271 uronide phase II metabolites from a rat thin tissue section was also illustrated.

272 omparisons by first testing if each animal's tissue section was sampled at a similar location and ena

273 al differences in ionization response across tissue sections was also investigated.

274 Lipid IMS on tissue sections was performed using MALDI-TOF/TOF MS in

275 s were performed by blinded researchers, and tissue sections were analyzed by local and blinded refer

276 Serial tissue sections were analyzed with anti-glial fibrillary

277 ue samples such as sea algae and mouse brain tissue sections were conducted using fixed DMS compensat

278 d the levels of CD68 positive macrophages in tissue sections were evaluated.

279 Ten-mum-thick tissue sections were floated onto Low-E (IR-reflective)

280 Tissue sections were incubated initially with GNR tagged

281 Tissue sections were stained for C5b-9, C4d, and laminin

282 The rats were killed, and cryosectioned tissue sections were subjected to hematoxylin and eosin

283 Ex-vivo mouse ileal tissue sections were treated with either EcN or the huma

284 Tissue sections were triple-labeled for the 65 kD isofor

285 arental cells, and human term placenta whole tissue sections were used as controls and for antibody v

286 en bovine brain stem, cortex, and cerebellum tissue sections were washed with a series of solvent sol

287 ndings for ubiquilin-1 and -2 in human brain tissue sections, where accumulation was observed in hunt

288 of mRNA localization in vivo and in ex-vivo tissue sections, which will facilitate mRNA trafficking

289 digestion can be performed on a single thin tissue section while preserving the relationship between

290 frozen mouse liver and rabbit adrenal gland tissue sections with a range of higher spatial resolutio

291 Imaging tissue sections with DESI MS shows that the 2-HG signal

292 way of imaging biomolecular distributions in tissue sections with high spectral and spatial resolutio

293 to ensure fast transfer of proteins from the tissue sections with minimal lateral diffusion to achiev

294 In whole-tissue sections with multiple HPV types, polymerase chai

295 orates liquid extraction from the surface of tissue sections with nanoelectrospray mass spectrometry.

296 aging for sensitive detection of the drug in tissue sections with subfemtomole sensitivity in each pi

297 in a single formalin-fixed paraffin-embedded tissue section, with accurate cell discrimination and sp

298 both brain glycogen and lactate in the same tissue section would benefit this research field.

299 hree cores per block (n = 1,286) or in whole tissue sections (WS; n = 516) by using standard immunohi

300 successfully in mapping different lipids in tissue sections, yet existing protocols fail to detect t