ライフサイエンスコーパス: staining

1 neutrophils and macrophages by histological staining.

2 erase chain reaction and immunohistochemical staining.

3 t microscopy after Maurits, Scarlet and Blue staining.

4 milar human-based score on hematoxylin-eosin staining.

5 ether (18)F-FDG uptake correlates with GLUT1 staining.

6 probe coupled with cardiac-specific antibody staining.

7 ina was examined using Hematoxylin and eosin staining.

8 diffusely for PD-L2 and showed sparse PD-L1 staining.

9 ools, was examined by intracellular cytokine staining.

10 arts for 2,3,5-triphenyltetrazolium chloride staining.

11 42 staining, annexin V/PI staining, and JC-1 staining.

12 on, Western blotting, and immunofluorescence staining.

13 ent TonEBP mice showed normal pattern of LC3 staining.

14 assay (ELISpot), and intracellular cytokine staining.

15 A scans with negative results had only 1+/2+ staining.

16 and eyes with superficial ODD showed nodular staining.

17 lorofluorescein (DCF), dihydroethidium (DHE) staining.

18 was further validated by immunohistochemical staining.

19 sion electron microscopy and picrosirius red staining.

20 ibrosis, and characteristic immunohistologic staining.

21 d immunospot assay or intracellular cytokine staining.

22 P-biotin nick end labeling assay and Hoechst staining.

23 transferase-mediated dUTP nick-end labeling staining.

24 assessed for necrosis with hematoxylin-eosin staining.

25 nfections without organisms detected by Gram staining.

26 hen compared to optimized immunofluorescence staining.

27 esolution without the need for sectioning or staining.

28 ng flow cytometry and intracellular cytokine staining after stimulation with phorbol myristate acetat

29 Immunofluorescence staining against AstA, AT, and TK in the brain revealed

30 Immunohistochemical staining against podoplanin and intratumoral platelet ag

31 s 1,000-fold more sensitive than Gag protein staining alone, with a detection limit of 0.5-1 Gagpol m

32 The immuno-staining analysis also showed that topoisomerase II is t

33 ath was measured by Hoechst/propidium iodide staining and activation of caspase-3.

34 elation between low frequencies of macroH2A1 staining and advanced, aggressive HCC subtypes with poor

35 Congo red staining and apple green birefringence demonstrated vitr

36 transcription, as shown by propidium iodide staining and BrUTP incorporation.

37 emonstrated less senescence by X-beta-Gal SA staining and by lower expression of p16.

38 by senescence-associated beta-Galactosidase staining and by Western blot analysis of p16.

39 cleotidyl transferase dUTP nick end labeling staining and caspase-3 activation.

40 g recognition as determined by CD1d multimer staining and CD1d-restricted functional responses.

41 gh alanine scanning, immunofluorescence cell staining and co-immunoprecipitation, we define a critica

42 a acquired from different sources, different staining and cutting protocols and different scanners.

43 d mononuclear cells (PBMCs) by intracellular staining and dual-secretion assay.

44 eric plexus presence by acetylcholinesterase staining and embryonic day 12.5 (E12.5) intestine transc

45 Analysis of Masson trichrome staining and fibrotic marker protein and mRNA expression

46 kines was analyzed by ELISA or intracellular staining and flow cytometry, and the expression of musca

47 as determined by indirect immunofluorescence staining and flow-cytometric analysis.

48 Microtome sectioning, differential staining and fluorescence microscopy were used to visual

49 va of the right eye for periodic acid-Schiff staining and from the left eye for MUC5AC mucin immunost

50 s and PSMA expression in immunohistochemical staining and generate a cutoff value for differentiation

51 yuridine (BrdU) assay, propidium iodide (PI) staining and growth curves, and blocks cell migration ba

52 Using Congo Red staining and hexadecane-aqueous buffer partitioning, the

53 Heart tissue was evaluated with vital staining and histologic examination.

54 Alizarin red staining and immunohistochemistry of GFP and osteocalcin

55 Consistently, immunohistochemical staining and in vitro binding assays showed that apoE co

56 d by morphometric quantitation of Sirius Red staining and increased mRNA levels of profibrotic genes,

57 Hdac3-deficient iNKT cells have less Cyto-ID staining and lower LC3A/B expression, indicative of redu

58 iver was established by immunohistochemistry staining and mass spectrometric analysis.

59 ological methods that include silver reduced staining and mass staining with dextran-conjugated dyes.

60 By combining fluorescent staining and microspectroscopy with software-based spect

61 caused by microneedle penetration following staining and optical imaging.

62 Retrospective analyses using PAS staining and PCR identified 3 and 3 more cases, respecti

63 ere reexamined by periodic acid-Schiff (PAS) staining and PCR to identify undiagnosed amoebic appendi

64 non-mineralised tissue can be enhanced using staining and phase contrast techniques.

65 rein, we utilized immunohistochemistry (IHC) staining and public microarray data analysis showing tha

66 Furthermore, phalloidin staining and reactive oxygen species estimation of Wnt5a

67 l fibrosis, as determined by Picrosirius Red staining and Second Harmonic Generation (SHG) Microscopy

68 phism (rs13266634) have decreased proinsulin staining and susceptibility to T2DM.

69 EETs and S aureus by using immunofluorescent staining and the PNA-Fish assay, respectively.

70 Immunohistochemical staining and Western blot analyses showed increased EZH2

71 resent study, we employed immunofluorescence staining and Western blot analysis to assess the express

72 re than 300 tumors using immunohistochemical staining and western blot.

73 ample-to-sample variability, due to antibody staining and/or instrument sensitivity, can introduce su

74 hocytes by double immunohistochemistry (PCNA-staining) and flow cytometry (BrdU incorporation) reveal

75 onjunction with immunohistochemistry, myelin staining, and a novel three-choice, reversal-learning ta

76 and silver methenamine, and picrosirius red staining, and CD31 and CD34 immunohistochemistry were ap

77 Cell apoptosis was detected by EB/AO staining, and cell cycle was analyzed by flow cytometry.

78 glycan deposition as assessed by Alcian blue staining, and gene expression of key anabolic proteins b

79 in reaction, dual-labeling immunofluorescent staining, and immunoassays.

80 assay, Hoechst 33342 staining, annexin V/PI staining, and JC-1 staining.

81 ndrial depolarisation was quantified by TMRE staining, and levels of DNA damage were compared in cell

82 electron microscopy (TEM) and Prussian Blue staining, and quantified using an iron specific colourim

83 mary epithelial proliferation, based on Ki67 staining, and suppressed tumor development.

84 drogenase (LDH) release assay, Hoechst 33342 staining, annexin V/PI staining, and JC-1 staining.

85 ELISA of cultured supernatants, and F-actin staining; apoptosis and efferocytosis by morphology and

86 ment, confirmed by Micro-CT and histological staining as well as expression of osteoblastic marker (O

87 a microscope-based propidium iodide/Hoechst staining assay assess only late stage membrane permeabil

88 olysis, cell viability, and AnnexinV-FITC/PI staining assays.

89 r stability, tear production, ocular surface staining, bulbar and limbal redness, tear volume, anteri

90 ified by cytology with hematoxylin and eosin staining but also provided molecular resolution through

91 The live/dead staining, cell proliferation assay and immunohistochemis

92 ic T cells, including intracellular cytokine staining, cell surface cytokine-capture assays, and stai

93 raphic atrophy (GA); and ultrastructural and staining characteristics of druse subtypes.

94 l transferase dUTP nick-end labeling (TUNEL) staining, circulating levels of alanine aminotransferase

95 pressed in the corticospinal tract and CHIT1 staining colocalised with markers of microglia (IBA1) an

96 Immunofluorescent staining confirmed that SFRP2 and FMO1 define cell types

97 athy was associated with increased caspase-3 staining, decreased CD3(+) T cells, and increased SIV-in

98 Immunohistochemical staining demonstrated that Ebf3 and Meis2 showed a restr

99 ography, 2,3,5-triphenyltetrazolium chloride staining determined infarct size, and fluorescence-activ

100 fter performing gammaH2AX immunofluorescence staining, DSBs were quantified with automated digital mi

101 ion with improved penetration properties and staining efficiency.

102 MS), native mass spectrometry, and negative-staining electron microscopy to comprehensively characte

103 culture, transfection, fixation, heavy-metal staining, embedding in resin, and EM imaging.

104 The method also works well for staining embryos, even late-stage embryos with cuticles,

105 opulation-averaged viability and trypan blue staining experiments.

106 atterns appear complementary, preferentially staining extramodular LCIC zones.

107 e and by the lack of antibodies suitable for staining FFPE tissue, primarily due to the inaccessibili

108 persed, and the intensity of apical membrane staining for AQP2 was reduced significantly (by approxim

109 In these animals, staining for beta-galactosidase (beta-gal) identifies ce

110 2 in the stromal compartment as well as high staining for CXCR4 and CXCR7 in the epithelial compartme

111 bined with mass spectrometry and verified by staining for direct protein-protein interaction, we find

112 GCA-positive group, 3 patients had positive staining for herpes zoster antigen.

113 messenger RNA (mRNA) expression and positive staining for IL-6.

114 (LVD) was determined by immunohistochemical staining for podoplanin.

115 fferentiate into osteoclasts was assessed by staining for tartrate-resistant acid phosphatase activit

116 in ATC patient tissues by immunofluorescent staining for the autophagy marker microtubule-associated

117 itu RNA hybridization combined with antibody staining for the HIV Gag protein.

118 Twist2-IKKbetaca lungs had increased staining for the vascular marker platelet endothelial ce

119 Immunohistochemical stainings for calprotectin in renal allograft biopsy spe

120 ugh mutation load and PD-L1 immune cell (IC) staining have been associated with response, they lack s

121 H2AX, Rad51, and HDAC4 by immunofluorescence staining; HDAC4, Rad51, and ubiquitin-conjugating enzyme

122 lbumin) extravasation, and hematoxylin-eosin staining helped detect only scattered extravasation of r

123 unospot (ELISPOT) and intracellular cytokine staining (ICS) in ZIKV-infected IFN-alpha/beta receptor-

124 The fluorescence staining identified the same particles as those found by

125 tribution of PLAG1 in the testis using X-gal staining; (ii) transcriptomic consequences of PLAG1 defi

126 re prominent in subsequent immunofluorescent staining images but not with classical hematoxylin and e

127 Double-staining immunohistochemistry showed CXCL9 co-localized

128 d and lesional morphea skin, and used double-staining immunohistochemistry to determine the cutaneous

129 alyzed by histology, immunoblots, phalloidin staining, immunohistochemistry, electron microscopy, and

130 correctly identified mislocalized or absent staining in 100% of the discovery cohort.

131 ithout intestinal disease, and levels of CD3 staining in all LSI animals strongly correlated with the

132 Immunohistochemical staining in an aromatase reporter mouse revealed that ma

133 t kidneys exhibited distinctly increased APA staining in areas of intact glomerular capillary loops.

134 with ranibizumab when compared with the VEGF staining in Case 2.

135 ty activity in cell line A-431 and low green staining in cells.

136 odendrocyte density and myelin basic protein staining in CNS lesions.

137 ed the levels of synaptophysin (SYP) protein staining in cortical (CTX) and hippocampal (HIPP) tissue

138 Significantly lower Iba-1 and Perls' iron staining in DP1(-/-) and laropiprant-treated WT groups w

139 Overexpression of miR-10b increased Ki-67 staining in human organ-cultured corneas and proliferati

140 ted defects in autophagic flux and lysosomal staining in human samples of type 2 diabetes.

141 ance (R2 = 0.76-0.99) when using chromogenic staining in isogenic cell lines.

142 % were positive for KLF5 (defined as nuclear staining in more than 5% of tumor cells).

143 man tumor biopsies showed significant fibrin staining in nearly all tumor types evaluated.

144 e, we examined, in the same sections, Kv3.1b staining in parvalbumin-positive interneurons, which sho

145 The novel location of C4d staining in proximity to liver sinusoidal endothelial ce

146 ip to calcitonin gene-related peptide (CGRP) staining in the dorsal horn.

147 conditioning, we observed increased beta-gal staining in the nucleus accumbens (NAC) shell and dorsal

148 greater than 5% positive immunohistochemical staining in the respective cell populations.

149 RK-10 shows staining in the tumor regions of FFPE tissues where the

150 iated with an increased alkaline phosphatase staining in the XLH cultures.

151 al iron deposits; this was proven with Perls staining in two patients.

152 ar hyperosmolarity, increased ocular surface staining, increased inflammation, symptomatic irritation

153 cytochrome c, and cleaved caspase-3 positive staining indicated that increased apoptosis involved a m

154 Histochemical GUS staining indicated that OsbHLH068 and AtbHLH112 share a

155 ical generator, was able to increase filipin staining indicating a link between ROS production and in

156 lesion exhibited increased filamentous actin staining, indicating active cell movement.

157 estinal segments studied revealed comparable staining intensities.

158 le amino acid substitution revealed that the staining intensity by anti-Valpha24 Abs depends on wheth

159 We also found a trend of increasing regional staining intensity for all positive GABAA receptor subun

160 usting for age, sex, and BCC location, PD-L1 staining intensity in tumor cells increased with the num

161 In PN sections (n = 31), median staining intensity was mild, median percentage of staine

162 tumour cells with membrane staining of >/=1+ staining intensity), and evaluable disease, who had not

163 try (>/= 25% of tumor cells with at least 2+ staining intensity).

164 stricted CASZ1 staining or low nuclear CASZ1 staining is found in tumor samples from patients with po

165 lex instrumentation and expertise while only staining isolated areas.

166 we compared lipid-, protein-, and RNA-based staining methods and developed a robust EV staining stra

167 Tissue microarray and microfluidics staining methods have emerged as powerful high throughpu

168 ely, and tartrate-resistant acid phosphatase staining notably was absent in the subarticular regions

169 umours (>/=25% of tumour cells with membrane staining of >/=1+ staining intensity), and evaluable dis

170 arboring CTNNB1 mutations have heterogeneous staining of beta-catenin and variable expression of gona

171 Cells with dual staining of both markers tended to be in well-to-moderat

172 Patients with higher dual-staining of CA19-9 and sTRA had statistically longer tim

173 ased expression of CTSB, as well as stronger staining of cathepsin B in the stratum granulosum of aff

174 of cell membranes, it controls the apparent staining of cells.

175 with the CPC core enzyme Aurora kinase B and staining of CPC components at centromeres is altered in

176 cell ELISA was used to establish the surface staining of CR-Kp strains.

177 damage, as measured by the CometChip and the staining of DNA double-strand break marker, gammaH2AX.

178 and transmission electron microscopy and by staining of filamentous actin.

179 ression was evaluated by immunohistochemical staining of formalin-fixed, paraffin-embedded sections.

180 icroscopy of glomeruli and immunofluorescent staining of glomerular epithelial cells (podocytes) indi

181 y immunohistochemical and immunofluorescence staining of hearts and aortas.

182 sequent immunohistochemistry and fluorescent staining of histological features.

183 eth cell deficiency was assessed by lysozyme staining of ileum tissues and lysozyme activity in fecal

184 Haematoxylin and eosin staining of infarcts showed well demarcated zones of oed

185 errogans Histological periodic acid-Schiff D staining of infected kidney showed interstitial nephriti

186 d blood/tissue partitioning by intravascular staining of leukocytes, we showed that both inflammatory

187 and temporal analyses of viral nucleoprotein staining of lung tissue sections and dissociated lung ce

188 Immunohistochemical staining of mice and human brain slices shows DAM with i

189 Immunohistological staining of occludin, Ki-67, NF-kappaB-p65, and terminal

190 Our exhaustive staining of paddlefish chromosomes combined with cytogen

191 Immunohistochemical staining of patient samples revealed that a significant

192 max, 5.1; range, 2.4-9.2) and correlative 3+ staining of prostatectomy specimens on PSMA immunohistoc

193 CD71/RNA double staining of reticulocytes enriched from adult peripheral

194 The cell imaging study revealed the staining of the cell and multicolor emission in the pres

195 Luxol fast blue staining of the corpus callosum was significantly greate

196 i-DNAJB9 antibody showed strong and specific staining of the glomerular tufts in a distribution that

197 Immunohistochemical staining of the hippocampus detected nBMP2 in the nuclei

198 En face staining of the murine aorta or carotid arteries modifie

199 Furthermore, immunohistochemical staining of the NFPAs clinical samples showed that the e

200 cous membrane cultures, and/or by culture or staining of the placenta or umbilical cord.

201 TJs of adjacent cells in immunofluorescence staining of the TJ molecules occludin and zonula occlude

202 Surface staining of the viral HA revealed that most cell populat

203 ge of primary tumor cells showing a positive staining of their nucleus or cytoplasm per 1 high-power

204 In patients, immunohistochemical staining of tissue microarrays and mRNA expression analy

205 Selective detection and staining of toxic amyloid plaques, a potential biomarker

206 Immunofluorescent staining of tumour sections from human oestrogen recepto

207 Immunofluorescence staining of ventral prostate tissue from obese HiMyc mic

208 ls to develop a reliable method for antibody staining of whole Drosophila larvae of any developmental

209 Immunohistochemical staining on formalin-fixed BCCs from a dermatology clini

210 g was also validated with immunofluorescence staining on Foxp3(+)CD4(+) and PD-1(+)CD8(+) T cells.

211 in vivo was confirmed by immunofluorescence staining on multinucleated cells at the bone surface of

212 Furthermore, podoplanin staining on stromal cells was more diffuse, and CXCL12 s

213 t with classical hematoxylin and eosin (H&E) staining on the same tissue section.

214 Without tissue staining or clearing, mPAM generates micrometer-resoluti

215 ub-micrometre level without the need for any staining or contrast agent.

216 erences were observed for phosphorylated tau staining or insoluble tau levels.

217 In contrast, cytoplasmic-restricted CASZ1 staining or low nuclear CASZ1 staining is found in tumor

218 with tear breakup time, corneal fluorescein staining, or ocular medications used by patients.

219 r205) and CP13 (pSer202) immunohistochemical stainings] pathological inclusions, neurofibrillary tang

220 tein 1, colocalize within a fingerprint-like staining pattern that correlates with ultrastructural mo

221 autoantibodies revealed a new sinusoidal C4d staining pattern when compared with HLA DSA (71% vs 3%;

222 As a conclusion, ACA displays a specific ANA staining pattern with a bimodal distribution, and ACA-po

223 The incorporation of the MYC staining patterns allowed the stratification of pRCC typ

224 combination with the MYC immunohistochemical staining patterns allows a more accurate prediction of p

225 ts with pRCC type 1 tumors and favorable MYC staining patterns died from tumor-related causes.

226 gnificantly higher levels than the other ANA staining patterns in both RA and healthy population (p <

227 ckout mice showed similar actin stress fiber staining patterns in unstimulated conditions.

228 thologic analysis illustrated characteristic staining patterns supporting a potential mechanism of tr

229 ion are cell transfection and a 2- to 45-min staining period with 3,3-diaminobenzidine (DAB) and hydr

230 hout destroying its function, simultaneously staining peripheral sensory structures and central axona

231 se 4 separate PD-L1 antibodies on 2 separate staining platforms and have their own scoring systems, w

232 Diagnosis of MCC was confirmed by staining positive for cytokeratin 20 (CK20) and synaptop

233 barrier without harming the cell during the staining process.

234 Zebrin staining produces alternating positive and negative stri

235 ions can be partially addressed by extending staining protocols to over a week (Drosophila brain) and

236 , was down-regulated, and its characteristic staining remained disrupted even at chronic phase.

237 panel, which are of major importance for the staining result.

238 with subsequently acquired immunofluorescent staining results.

239 Congo red staining revealed brilliant red amyloid deposits confirm

240 Tau staining revealed neuronal pretangle forms and glial tau

241 Examination by SDS-PAGE followed by protein staining revealed protein profiles indicative of severe

242 icroCT, alizarin red/alcian blue and calcein staining revealed severe skeletal deformity, presence of

243 3 cell types by means of immunofluorescence staining, RT-PCR, and qRT-PCR, and qRT-PCR analysis reve

244 esia) >/=1 and </=10 mm, corneal fluorescein staining score >/=2.0 (0-4 scale), eye dryness score (ED

245 Staining showed decreased fibrosis and improved angiogen

246 Immunohistochemical staining showed increased expression of pSMAD158 and VEG

247 crescent formation, and nuclear phospho-p65 staining showed NF-kappaB activation within CD31-express

248 analysis in conjunction with GABA-immunogold staining showed that (1) GAD-positive terminals mainly t

249 Ecocardiography and Masson staining showed that ZYZ-168 substantially improved card

250 The JC-1 staining shows the mitochondrial membrane potential is d

251 d staining methods and developed a robust EV staining strategy, with the amine-reactive fluorescent l

252 IM1 antibodies on TRPC1-based SOCs and STIM1 staining suggest that channel activation may involve ins

253 slight yet statistically significantly lower staining than either 28-8 or E1L3N, but this significanc

254 n exhibited a more prominent immuno-positive staining that correlated with rRNA transcription, as sho

255 abeling (TUNEL) and phospho-histone H3 (PH3) staining to assess apoptosis and cell proliferation, res

256 re examined first by hematoxylin-eosin (H&E) staining to establish the diagnosis of GCA.

257 We used hematoxylin-eosin staining to examine cochlear histopathological changes.

258 use of neuron-specific promoters can direct staining to mammalian neurons to provide clear detection

259 computational method on pan-cytokeratin IHC stainings to quantify tumor fragmentation (TF), a measur

260 roscopy and fluorescence detection (Nile Red staining) to interrogate Mycobacterium tuberculosis cell

261 Here we use thioflavin T staining, transmission electron microscopy, as well as i

262 Golgi staining, ultra-structural and electrophysiological stud

263 Double immunofluorescence staining using antibodies against choline-acetyltransfer

264 Double staining using in situ hybridization and immunocytochemi

265 PSMA staining was added for representative sections in RP spe

266 ere ERG-positive, and being negative for ERG staining was associated with higher Gleason score.

267 Hematoxylin and eosin staining was done to verify the presence of lymphatic me

268 n stromal cells was more diffuse, and CXCL12 staining was dramatically reduced in Il-17ra(-/-) mice p

269 However, the intensity of wtp53 staining was generally weaker than that of p53R172H, whi

270 However, staining was heterogeneous across and within tumor types

271 Wild-type TTR staining was less prominent in TTR-FAP patients.

272 ol had no impact and reactive oxygen species staining was negligible in KK.

273 OSM staining was observed in NPs, showed colocalization with

274 Less VEGF staining was observed within the retina of the eyes trea

275 In the posterior pole, positive staining was only observed at the level of the nerve fib

276 integrity, aurophosphate (Black Gold) myelin staining was performed on mPFC sections.

277 In two patients, Perls staining was performed on tissue samples from the LSIR.

278 ith nuclear polarization, but exclusive sTRA staining was present in small clusters of cells with poo

279 Positive staining was present within the nerve fiber layer, inner

280 use of paper point sampling and fluorescence staining was shown to be a rapid method, able to detect

281 Immunohistochemical staining was used to identify active JCPyV infection wit

282 nce of macrophages, CD68 immunohistochemical staining was used.

283 d with diabetes, in combination with insulin staining, was performed to assess beta-cell selectivity

284 Using triple immunofluorescence staining we tested whether there were alterations in the

285 Using immunofluorescence staining, we confirmed the expression of ecto-5'-nucleot

286 Using cell membrane staining, we investigated the spatial distribution of Co

287 with more than 10% and 1% nuclear tumor cell staining were considered, respectively, AR- and ER-posit

288 but histologic findings at hematoxylin-eosin staining were normal.

289 Hematoxylin and eosin and Oil Red O staining were performed to determine steatosis.

290 with COPD was assessed by immunofluorescence staining, Western blot analysis, and ELISA.

291 Staining with an antibody against M2FA demonstrated that

292 Immunohistochemical staining with an antibody specific for anti-PD-L1 (22C3)

293 Immunofluorescence staining with anti-alpha-tubulin antibodies and cell cyc

294 hat include silver reduced staining and mass staining with dextran-conjugated dyes.

295 fic B cells were identified using dual-color staining with fluorescently labeled PLA.

296 However, we found that staining with MitoTracker Green, a commonly used dye to

297 ls and sub-G1 populations as well as nuclear staining with orange fluorescence of treated cancer cell

298 g, cell surface cytokine-capture assays, and staining with peptide:MHC class II multimers, all of the

299 Finally, human AAA samples had stronger staining with the antibodies against 3-HAA, IDO, and kyn

300 ermeabilized WT myocytes showed little or no staining, without striation.