ライフサイエンスコーパス: hematoxylin

1 verity of inflammation was assessed by eosin/hematoxylin.

2 clear marker (NeuN), and counterstained with hematoxylin.

3 In 12 cadavers, specimens were stained with hematoxylin and eosin (3 sections) or Masson trichrome (

4 ) previously had biopsies submitted for both hematoxylin and eosin (H & E) and direct IF testing.

5 Routine hematoxylin and eosin (H & E) staining and direct immuno

6 Hematoxylin and eosin (H & E) staining was performed to

7 Hematoxylin and eosin (H & E) staining was then performe

8 dded lacrimal glands (LGs) were stained with hematoxylin and eosin (H&E) and evaluated with a stereom

9 Hematoxylin and eosin (H&E) and immunohistochemical anal

10 Serial sections were then stained with hematoxylin and eosin (H&E) and subjected to detailed mo

11 al examination of the explanted livers using hematoxylin and eosin (H&E) and Tdt-mediated UTP nick-en

12 tumor cells or cell aggregates identified by hematoxylin and eosin (H&E) and/or IHC.

13 novel OCT system and verified the results by hematoxylin and eosin (H&E) histology.

14 The prognostic value of ultrastaging hematoxylin and eosin (H&E) negative LNs (N0) using pan-

15 ing (SRS) imaging technique and a new pseudo-hematoxylin and eosin (H&E) recoloring methodology.

16 stromal-immune interface across 400 melanoma hematoxylin and eosin (H&E) specimens from The Cancer Ge

17 Application of digital image analysis from hematoxylin and eosin (H&E) stain to multiplex labeling

18 The algorithm was tested using digitized hematoxylin and eosin (H&E) stained prostate cancer spec

19 ificance of TILAb score on digitized WSIs of Hematoxylin and Eosin (H&E) stained slides of OSCC patie

20 scent staining images but not with classical hematoxylin and eosin (H&E) staining on the same tissue

21 Hematoxylin and eosin (H&E) staining, confocal microscop

22 In contrast, hematoxylin and eosin (H&E) staining-which highlights ce

23 2 maps and were histologically identified by hematoxylin and eosin (H&E) staining.

24 s was performed using immunofluorescence and hematoxylin and eosin (H&E) staining.

25 zation, and histopathological abnormities by hematoxylin and eosin (H&E) staining.

26 Enucleated eyes were processed for hematoxylin and eosin (H&E) staining.

27 for histopathological analysis with routine hematoxylin and eosin (H&E) staining.

28 Here, we compared fluorojade B (FJB) and hematoxylin and eosin (H&E) stains primarily to examine

29 icobacter pylori IgG-antibody titer changes, hematoxylin and eosin (H&E) stains, immunohistochemical

30 2,3,5-triphenyltetrazolium chloride (TTC) or hematoxylin and eosin (H&E) stains.

31 ct comparison between H&E alone and elastica Hematoxylin and Eosin (H&E) was made in 53 patients.

32 Tissue sections were stained with hematoxylin and eosin (H&E), and DNA was extracted from

33 osections were prepared for autoradiography, hematoxylin and eosin (H&E), and immunofluorescence stai

34 ed only on the analysis of WSIs stained with hematoxylin and eosin (H&E), even though there is additi

35 sies stained with three histological stains: hematoxylin and eosin (H&E), Masson's trichrome, and ret

36 ion (SHIFT) which takes histologic images of hematoxylin and eosin (H&E)-stained tissue as input, the

37 erial tissue sections that were stained with hematoxylin and eosin (H&E).

38 ed sections of the samples were stained with hematoxylin and eosin (HE) and subjected to histomorphom

39 Hematoxylin and eosin (HE) staining of cerebral tissue w

40 The SN was examined first by hematoxylin and eosin (HE), and if the SN was negative w

41 Liver damage was assessed by hematoxylin and eosin and alanine aminotransferase level

42 Every fifth section was stained with hematoxylin and eosin and analyzed histologically.

43 Specimens were stained using hematoxylin and eosin and by immunohistochemistry for cy

44 were selected for histologic analysis using hematoxylin and eosin and dihydroxyphenylalanine oxidase

45 Brain sections at 7 days were examined via hematoxylin and eosin and Fluoro-Jade C (identifying dyi

46 the excised left kidney tissue stained with hematoxylin and eosin and Gomori's methenamine silver st

47 Hematoxylin and eosin and immunohistochemical analyses s

48 rwent frozen sectioning and were examined by hematoxylin and eosin and immunohistologic (cytokeratin)

49 ion of different regions of the retina using hematoxylin and eosin and immunostaining.

50 Hematoxylin and eosin and Masson trichrome staining show

51 The results of hematoxylin and eosin and Masson's trichrome staining as

52 s evaluated through histologic staining with hematoxylin and eosin and oil red O and also by quantita

53 Hematoxylin and eosin and Oil Red O staining were perfor

54 cumulation and liver injury, as evidenced by hematoxylin and eosin and Oil Red O staining.

55 ns were routinely processed and stained with hematoxylin and eosin and periodic acid Schiff.

56 were assessed by means of flow cytometry and hematoxylin and eosin and periodic acid-Schiff staining,

57 and lung biopsy specimens were stained with hematoxylin and eosin and periodic acid-Schiff, visualiz

58 tions were stained with Masson trichrome and hematoxylin and eosin and subjected to the tartrate-resi

59 also performed on Tax(+) mouse tails, using hematoxylin and eosin and tartrate-resistant acid phosph

60 eoclast (OCS) accumulation were evaluated by hematoxylin and eosin and tartrate-resistant acid phosph

61 munohistochemistry (IHC) and inflammation by hematoxylin and eosin and trichrome staining, IHC, and i

62 were cultured, and microscopic analysis with hematoxylin and eosin and trichrome was performed.

63 re made of each cut surface and stained with hematoxylin and eosin and/or Diff-Quik.

64 cted changes in histology were determined by hematoxylin and eosin as well as by Fluoro-Jade staining

65 ibiting close correlation with corresponding hematoxylin and eosin histology.

66 specimens imaged using both SRH and standard hematoxylin and eosin histology.

67 ls or colocalization analysis on brightfield hematoxylin and eosin images, which is useful for unders

68 umor diagnostic imaging is commonly based on hematoxylin and eosin or immunohistochemical staining of

69 Thin sections (5 microm) were stained with hematoxylin and eosin or tartrate-resistant acid phospha

70 Hind limb sections were stained with hematoxylin and eosin or toluidine blue and scored for i

71 jury, as indicated by Sirius Red/Fast Green, hematoxylin and eosin quantification, and serum alanine/

72 In 319 patients with both frozen-section hematoxylin and eosin results and BLN Assay results, the

73 develop CNN architectures to analyze 27,815 hematoxylin and eosin scanned images from The Cancer Gen

74 Anatomy was assessed by serial hematoxylin and eosin sections and scanning electron mic

75 and can be readily identified using routine hematoxylin and eosin sections, we suggest that pathway

76 ASS1 + HCA combined with a typical hematoxylin and eosin stain aspect defined a new HCA sub

77 Hematoxylin and eosin stain revealed a paucity of connec

78 ally and clinically node-negative by routine hematoxylin and eosin stain, 100 patients were found to

79 were killed at 7 days and injured neurons in hematoxylin and eosin stained coronal brain sections thr

80 ion of histologic features relying solely on hematoxylin and eosin stained pancreatic tissue sections

81 related with histopathological assessment of hematoxylin and eosin stained thin tissue sections obtai

82 of occult nodal metastases not identified by hematoxylin and eosin staining (H&E).

83 Hematoxylin and eosin staining and histologic grading fo

84 on of a cell block is desirable to allow for hematoxylin and eosin staining and immunohistochemical a

85 omposition, and cytokine expression by using hematoxylin and eosin staining and immunohistochemistry.

86 osectioned tissue sections were subjected to hematoxylin and eosin staining and MALDI-MSI analyses.

87 Hematoxylin and eosin staining and smooth muscle actin (

88 Histological examination with hematoxylin and eosin staining and von Kossa staining co

89 changes that are identified by cytology with hematoxylin and eosin staining but also provided molecul

90 Hematoxylin and eosin staining confirmed marked synovial

91 hen stained to reveal tumor pathophysiology: Hematoxylin and eosin staining demonstrated viable and n

92 h categories were examined with conventional hematoxylin and eosin staining for epithelial, connectiv

93 eased apoptosis by both active caspase 3 and hematoxylin and eosin staining in both the intestinal ep

94 valuation by means of light microscopy after hematoxylin and eosin staining might not accurately refl

95 al signs of muscular dystrophy, as judged by hematoxylin and eosin staining of muscle biopsies taken

96 in whole eye flatmounts was quantified, and hematoxylin and eosin staining of paraffin sections was

97 rkflow for intraoperative diagnosis based on hematoxylin and eosin staining of processed tissue is ti

98 and three quantitative characteristics from hematoxylin and eosin staining of prostate tissue.

99 Hematoxylin and eosin staining of treated tissues did no

100 Hematoxylin and eosin staining revealed intact colonic e

101 Furthermore, hematoxylin and eosin staining revealed necrotic cell de

102 Hematoxylin and eosin staining revealed similar nuclear

103 Hematoxylin and eosin staining revealed that moderate to

104 Hematoxylin and eosin staining showed clear signs of vas

105 Hematoxylin and eosin staining showed epithelial migrati

106 Hematoxylin and eosin staining showed no differences in

107 leukocyte, liver, and jejunum DNA damage and hematoxylin and eosin staining to investigate macroscopi

108 Hematoxylin and eosin staining was done to verify the pr

109 biopsies were analyzed for histomorphology (hematoxylin and eosin staining) and DNA damage (terminal

110 biopsies were analyzed for histomorphology (hematoxylin and eosin staining) and markers of apoptosis

111 romote microglial activation as confirmed by hematoxylin and eosin staining, (3)H-PK11195 autoradiogr

112 the extent of surface hemorrhage/contusion, Hematoxylin and Eosin staining, and behavioral deficits

113 ,3,5-triphenyltetrazolium chloride staining, hematoxylin and eosin staining, and terminal deoxynucleo

114 Histological examination included hematoxylin and eosin staining, immunofluorescence, immu

115 ens and corneal development were assessed by hematoxylin and eosin staining, in situ hybridization, a

116 d-type control animals was examined by using hematoxylin and eosin staining.

117 ures closely resembling histopathology using hematoxylin and eosin staining.

118 examined by immunohistochemical analysis and hematoxylin and eosin staining.

119 s; structural mucosal damage was measured by hematoxylin and eosin staining.

120 h slit lamp, digital confocal microscopy and hematoxylin and eosin staining.

121 Mouse eye morphology was assessed by hematoxylin and eosin staining.

122 y knee biopsy and assessed histologically by hematoxylin and eosin staining.

123 ally and neuronal integrity was assessed via hematoxylin and eosin staining.

124 l structure of the retina was examined using Hematoxylin and eosin staining.

125 d is usually incompatible with commonly used hematoxylin and eosin staining.

126 Morphology (hematoxylin and eosin), apoptosis (M30), tight junctions

127 ic data (e.g., images of cell proliferation, hematoxylin and eosin).

128 ing an abdominal reexploration, stained with hematoxylin and eosin, and evaluated according to a semi

129 ning plastic sections with toluidine blue or hematoxylin and eosin, and show how to couple these stai

130 formalin, embedded in paraffin, stained with hematoxylin and eosin, and/or fresh frozen.

131 histopathologic evaluation of organ injury (hematoxylin and eosin, electron microscopy) and immunohi

132 cytokines, and osteoclasts was assessed from hematoxylin and eosin, immunohistochemical, or tartrate-

133 n, intracellular Ca(2+) handling, histology (hematoxylin and eosin, Masson trichrome), protein damage

134 Tissue of resected HCCs was stained for hematoxylin and eosin, Masson trichrome, alpha-smooth mu

135 reated mice as shown by transaminase levels, hematoxylin and eosin, Masson's trichrome staining, and

136 Standard hematoxylin and eosin, periodic acid-Schiff and silver m

137 Kidneys were harvested for histology (hematoxylin and eosin, periodic acid-Schiff) and termina

138 Gram staining, bright-field microscopy, hematoxylin and eosin, periodic acid-Schiff, Congo red,

139 Hematoxylin and eosin, Prussian blue and ED-1, a monoclo

140 Hematoxylin and eosin, S100, and smooth muscle actin imm

141 Eye sections were stained with hematoxylin and eosin, Schiff reagent, and fluorescein,

142 The microscopic slides were stained with hematoxylin and eosin, special stains for organisms, and

143 Sections were stained with hematoxylin and eosin, tissue gram stain, and immunostai

144 In this study, we collect hematoxylin and eosin- stained histopathology whole-slid

145 A-derived purity, leukocyte methylation, and hematoxylin and eosin-derived lymphocyte counts) and cel

146 n the epithelium) were examined by reviewing hematoxylin and eosin-stained biopsies and by immunohist

147 19 (16%) had morphologic evidence of HCL in hematoxylin and eosin-stained bone marrow sections.

148 Hematoxylin and eosin-stained histologic sections were u

149 rmanent sections were evaluated with up to 4 hematoxylin and eosin-stained levels and cytokeratin imm

150 yorrhexis, and red blood cells from standard hematoxylin and eosin-stained pathology images in lung a

151 Hematoxylin and eosin-stained plastic sections were used

152 tmounts and by counting preretinal nuclei of hematoxylin and eosin-stained retinal sections, respecti

153 One hematoxylin and eosin-stained section of the resected pr

154 Full-face hematoxylin and eosin-stained sections of 506 tumors fro

155 Microscopic examination of hematoxylin and eosin-stained sections revealed non-case

156 In addition to the macroscopic analyses, hematoxylin and eosin-stained sections were used to stud

157 Morphologic analyses were conducted on hematoxylin and eosin-stained sections.

158 und surface and inflammation was assessed on hematoxylin and eosin-stained sections.

159 l diagnosis, three pathologists examined the hematoxylin and eosin-stained slides of the known DIF-po

160 Demineralized and hematoxylin and eosin-stained tissues at developmental s

161 lve ophthalmic pathologists analyzed scanned hematoxylin and eosin-stained virtual microscopic slides

162 Sections were routinely stained with hematoxylin and eosin.

163 es from each specimen were also stained with hematoxylin and eosin.

164 the alpha-camera and the other stained with hematoxylin and eosin.

165 specimens were decalcified and stained with hematoxylin and eosin.

166 yes, and paraffin sections were stained with hematoxylin and eosin.

167 examined histologically after staining with hematoxylin and eosin.

168 Multiple serial sections were stained with hematoxylin and eosin.

169 can be reliably used on tissue stained with hematoxylin and eosin.

170 imaged with autoradiography and stained with hematoxylin and eosin.

171 mage in cardiac tissue sections stained with hematoxylin and eosin.

172 In parallel, RTDs were stained with hematoxylin and periodic acid Schiff to determine pericy

173 plying the electrochemical signal generator, hematoxylin and the peak current of differential pulse v

174 staining methods: Hematoxylin &Eosin, CD31 &Hematoxylin, and Ki-67 and where most of the nuclei were

175 )Cu-NOTA-AE105 was confirmed by alignment of hematoxylin- and eosin-stained and uPAR immunohistochemi

176 or of histopathologic response was scored on hematoxylin- and eosin-stained sections of the surgical

177 , Hoechst fluorescence vascular imaging, and hematoxylin-and-eosin histology-were superimposed, evalu

178 cence assessment was far more sensitive than hematoxylin-and-eosin staining in detecting small MDBs,

179 Hematoxylin-and-eosin staining showed viable grafts in 9

180 MDB formation was compared using hematoxylin-and-eosin staining, or immunofluorescence st

181 Decalcified, hematoxylin-and-eosin-stained cross-sections of the defe

182 f an inflammatory infiltrate was measured in hematoxylin-and-eosin-stained sections.

183 Due to the intercalation mechanism of hematoxylin-DNA interaction, the detachment of aptamer f

184 ed skin cancer is microscopic examination of hematoxylin & eosin stained tissue by a pathologist.

185 arvested for mechanical tests, histological (Hematoxylin & Eosin, and Masson's Trichrome) and immunoh

186 ree cohorts with different staining methods: Hematoxylin &Eosin, CD31 &Hematoxylin, and Ki-67 and whe

187 Gross inspection, slicing, and hematoxylin-eosin (10 specimens) and nicotinamide adenin

188 ded temporal arteries were examined first by hematoxylin-eosin (H&E) staining to establish the diagno

189 dye and/or radiotracer and were examined by hematoxylin-eosin (H&E) staining, cytokeratin immunohist

190 riphenyltetrazolium chloride (TTC) staining, hematoxylin-eosin (H&E) staining, the terminal deoxyribo

191 burden, sections were processed for standard hematoxylin-eosin (H&E) staining.

192 oidal thickness and area were measured after hematoxylin-eosin (H&E) staining.

193 uclear layer (ONL) thickness was measured on hematoxylin-eosin (H&E)-stained sections, and apoptosis

194 Sections were scored for TILs on hematoxylin-eosin (H&E)-stained sections, and immunohist

195 Hematoxylin-eosin (H-E) staining was performed on three

196 block, 3 sequential slides were stained with hematoxylin-eosin (H-E), melanoma antigen (melan-A), and

197 with immunohistochemical analysis, including hematoxylin-eosin (H-E), Von Kossa, and von Willibrand f

198 Hematoxylin-eosin (HE) and immunohistochemical staining

199 ation into hepatic DNA, the mitotic index in hematoxylin-eosin (HE) sections and by immunochemical de

200 every patient with colorectal cancer (CRC), hematoxylin-eosin (HE)-stained tissue slides are availab

201 Sections were stained with hematoxylin-eosin and exposed to immunohistochemistry fo

202 Neuronal damage was subsequently assessed by hematoxylin-eosin and Fluoro-Jade B staining.

203 opsy specimens from all lesions stained with hematoxylin-eosin and immunohistochemical markers (melan

204 Hematoxylin-eosin and immunohistochemical stainings for

205 upstaged 48 of 161 histopathology-negative (hematoxylin-eosin and immunohistochemistry) SLN specimen

206 The biopsy specimens were stained with hematoxylin-eosin and immunostained for Musashi-1 (Msi-1

207 Brain sections were stained with hematoxylin-eosin and Luxol fast blue.

208 after paraffin embedding, and staining with hematoxylin-eosin and Movat pentachrome.

209 IHC) are visualized as inclusion bodies with hematoxylin-eosin and nucleic acid stains and in methyle

210 Hematoxylin-eosin and PAX8 immunohistochemical stains we

211 HP was performed on hematoxylin-eosin and periodic acid Schiff-stained secti

212 Histopathologic analysis was performed on hematoxylin-eosin and periodic acid-Schiff sections.

213 made from all the samples and stained using hematoxylin-eosin and periodic acid-Schiff stains.

214 d at 5 and 10 days post-PHX, as indicated by hematoxylin-eosin and proliferating cell nuclear antigen

215 stological analyses of sections stained with hematoxylin-eosin and tartrate-resistant acid phosphatas

216 At 2 wk, hematoxylin-eosin and terminal deoxynucleotidyl transfer

217 from infected control animals, stained with hematoxylin-eosin and the Gram stain, showed edema and/o

218 multilevel sectioning and were stained with hematoxylin-eosin and the pancytokeratin marker AE1/AE3.

219 Histologic appearance (hematoxylin-eosin and trichrome staining) and presence o

220 Slides stained with hematoxylin-eosin and trichrome were evaluated by two li

221 eth processed for histologic evaluation with hematoxylin-eosin and Verhoeff's stains.

222 imonidazole, sirius red, cytokeratin 14, and hematoxylin-eosin for quantitative assessment of hypoxia

223 samples should be made available for routine hematoxylin-eosin histopathological evaluation until the

224 Sentinel lymph node specimens (hematoxylin-eosin negative) and bone marrow specimens we

225 ed, and alternate sections were stained with hematoxylin-eosin or stained for GFP expression.

226 orrelated with hyperplasia of melanocytes in hematoxylin-eosin sections (kappa = 0.422, P < .001).

227 filtrating lymphocytes (TILs) were scored in hematoxylin-eosin slides using current consensus guideli

228 ks of acquired specimens were examined using hematoxylin-eosin stain and double immunostain using HMB

229 Histologic slides (hematoxylin-eosin stain) from three resected rotator cuf

230 image-based automated assessment of TILs on hematoxylin-eosin stained sections in melanoma.

231 formed by using standard light microscopy on hematoxylin-eosin stained specimens; immunohistochemistr

232 reported in the anatomic diagnosis, based on hematoxylin-eosin staining alone, for three (8%) of the

233 The corneal buttons were then evaluated by hematoxylin-eosin staining and by immunostaining with ma

234 Hematoxylin-eosin staining confirmed that all spots with

235 Histology of heart sections included hematoxylin-eosin staining for overt damage, immunofluor

236 to macromolecule albumin) extravasation, and hematoxylin-eosin staining helped detect only scattered

237 Histologic data from hematoxylin-eosin staining of explanted liver specimens

238 Immunohistochemical and hematoxylin-eosin staining of liver sections was perform

239 ied by frozen section, touch preparation, or hematoxylin-eosin staining on permanent section.

240 stochemically positive or negative [IHC+/-], hematoxylin-eosin staining positive or negative [H & E +

241 Hematoxylin-eosin staining showed that neuronal injury i

242 Histologic examination with hematoxylin-eosin staining showed that results of 36 (67

243 We used hematoxylin-eosin staining to examine cochlear histopath

244 Hematoxylin-eosin staining was also performed.

245 as evaluated and histologic examination with hematoxylin-eosin staining was performed at 4 hours, 24

246 stroduodenoscopy, but histologic findings at hematoxylin-eosin staining were normal.

247 Autoradiography and hematoxylin-eosin staining were performed on the dissect

248 x vivo both for inflammation grade (by using hematoxylin-eosin staining) and for expression of select

249 ivo by means of histologic examination (with hematoxylin-eosin staining) and immunostaining of vascul

250 (reduced alanine transferase) and necrosis (hematoxylin-eosin staining) compared with the HSP27 WT m

251 tive histological assessment of liver lipid (hematoxylin-eosin staining), inflammation (galectin-3 im

252 At hematoxylin-eosin staining, coagulation necrosis was obs

253 ses were performed with specific techniques (hematoxylin-eosin staining, terminal deoxynucleotidyl tr

254 ent to those containing VZV were examined by hematoxylin-eosin staining.

255 (98.3%), 3904 (76.3%) were tumor-negative by hematoxylin-eosin staining.

256 Tumors were assessed for necrosis with hematoxylin-eosin staining.

257 e of TF using a similar human-based score on hematoxylin-eosin staining.

258 Finally, coregistration of histologic hematoxylin-eosin stains with autoradiography signals fr

259 ned with isolectin B4, Masson trichrome, and hematoxylin-eosin were used to characterize injured myoc

260 c, major histocompatability complex class I, hematoxylin-eosin).

261 icrom) along the coronal plane, stained with hematoxylin-eosin, and visualized by conventional light

262 GI was quantified on hematoxylin-eosin, CD3, CD20, and CD68 stains on biopsie

263 RPM specimens from 7 eyes were stained with hematoxylin-eosin, cytokeratin 7, cytokeratin AE1/3, smo

264 egration, or regeneration was analyzed using hematoxylin-eosin, immunohistochemical staining, and cel

265 Hematoxylin-eosin, Masson trichrome, and biotinylated is

266 pathologic findings in sections stained with hematoxylin-eosin, periodic acid-Schiff (PAS) reaction,

267 araffin-embedded tissues and correlated with hematoxylin-eosin, periodic acid-Schiff (PAS), and mucic

268 pecimen was examined following staining with hematoxylin-eosin, periodic acid-Schiff, and Gram stain.

269 Sections of the liver were examined with hematoxylin-eosin, periodic acid-Schiff, Masson trichrom

270 tained using a variety of methods, including hematoxylin-eosin, periodic acid-Schiff, methenamine sil

271 anine aminotransferase) and liver histology (hematoxylin-eosin, Sudan III) were determined to monitor

272 Histopathologic slides were evaluated with hematoxylin-eosin, trichrome, and elastin stains.

273 evaluated levels of percentage of TILs using hematoxylin-eosin-stained core biopsy sections taken at

274 luorescence images, NADH-stained images, and hematoxylin-eosin-stained images were compared.

275 Staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr

276 nts using staged excision with comprehensive hematoxylin-eosin-stained permanent section margin contr

277 Standard hematoxylin-eosin-stained sections and immunohistochemic

278 re studied by (i) microscopic examination of hematoxylin-eosin-stained sections for inflammation and

279 Hematoxylin-eosin-stained sections of the same transplan

280 After resection, whole-mount hematoxylin-eosin-stained sections were registered to th

281 (1) Review of clinical data and hematoxylin-eosin-stained sections with (2) immunohistoc

282 Review of clinical data, hematoxylin-eosin-stained sections, and immunohistochemi

283 Hematoxylin-eosin-stained slices of mammary tissues were

284 and inflammatory cell counts were counted on hematoxylin-eosin-stained slides and osteoclasts were co

285 Stromal TILs were assessed on whole-section hematoxylin-eosin-stained slides using a dichotomized cu

286 issue sections and/or detection of amebas in hematoxylin-eosin-stained slides.

287 Hematoxylin-eosin-stained tumor slides from patients wit

288 uted tomography (CT) and light microscopy of hematoxylin-eosin-stained tumor tissue were compared.

289 erated and compared with digitized images of hematoxylin-eosin-stained whole-mount histologic slices.

290 ed in each specimen on routine staining with hematoxylin-eosin.

291 Hematoxylin/eosin and toluidine blue staining and atomic

292 lso applying a specific DNA probe as well as hematoxylin for electrochemical indicator.

293 d to diagnose LSCD than the conventional PAS-hematoxylin method, although a minimum RNA concentration

294 dium); they were tested with trichrome, iron-hematoxylin, or modified acid-fast stains or the Meridia

295 Histologic analysis was performed by hematoxylin-phloxine-safran staining, followed by immuno

296 et cells in the cornea was determined by PAS-hematoxylin staining, whereas the presence of the MUC5AC

297 ples were also available for comparative PAS-hematoxylin staining.

298 drug uptake and subsequent visualization on hematoxylin staining.

299 preretinal nuclei were quantified by PAS and hematoxylin staining.

300 Nissl and hematoxylin stains provided little information regarding